1. Single-cell RNA sequencing was performed on hematopoietic stem cells isolated from myelodysplastic syndrome patients and normal individuals to characterize heterogeneity. Cells were collected before and after treatment with decitabine from responders and non-responders.
2. Differential expression analysis identified genes dysregulated in MDS compared to normal, including pathways involved in hematopoiesis. Clusters of patients were identified based on expression of hematopoietic stem cell signature genes.
3. The study aims to understand heterogeneity in MDS, factors influencing response to therapy, and disease progression by characterizing gene expression profiles at the single-cell level. This may help identify new therapeutic targets.
The CRISPR/Cas9 system has emerged as one of the leading tools for modifying genomes of organisms ranging from E. coli to humans. Additionally, the simple gene targeting mechanism of CRISPR technology has been modified and adapted to other applications that include gene regulation, detection of intercellular trafficking, and pathogen detection. With a wealth of methods for introducing Cas9 and gRNAs into cells, it can be challenging to decide where to start. In this presentation, Dr Adam Clore describes the CRISPR mechanism and some of the most prominent uses for CRISPR, along with methods where IDT technologies can assist scientists in designing, testing, and executing a variety of CRISPR-mediated experiments. For more informaton, visit: http://www.idtdna.com/crispr
KromaTiD's directional genomic hybridization (dGH) platform uses single-stranded probes to discover, detect, and diagnose structural variants like inversions and translocations at high resolution on a cell-by-cell basis. This complements next-generation sequencing and microarrays. dGH assays can find inherited, spontaneous, and induced mutations. PinPoint FISH assays then allow targeted detection of variants identified by dGH. KromaTiD offers both research services using its techniques and collaboration with customer labs.
Lessons learned from high throughput CRISPR targeting in human cell linesChris Thorne
In just a short period of time CRISPR-Cas9 technology has revolutionized the field of genome editing, and taken the scientific community by storm. Already our understanding of how best to apply this technology has advanced significantly and almost every week new publications appear showcasing its application in basic and translational research.
While CRISPR-Cas9 is applicable across many different cell types, we have found it particularly suited for genome editing in near-haploid human cell lines. This has allowed us to establish a robust pipeline for the inactivation of non-essential genes at unprecedented scale and efficiency.
We have now knocked out over 1500 human genes and have generated a resource that is, to the best of our knowledge, the largest collection of human knockout cell lines available, covering comprehensive subsets of genes clustered by biological pathway (e.g. the autophagy pathway, the JAK/STAT pathway) or by phylogenetic relationship (e.g. kinases, bromodomain-containing proteins).
In this talk we will discuss how, through more than 1500 genome editing experiments, we have started to unravel some of the general principles governing the use of CRISPR-Cas9 in mammalian cells. For example, we have analyzed the impact of variation in the guide RNA sequence on Cas9 cleavage efficiency and characterized the mutational signature arising from CRISPR-Cas9 cleavage.
We will also highlight (with examples) how these learnings are now being applied to introduce other genomic modifications in a high throughput manner, including chromosomal deletions, translocations, point mutations and endogenous gene tags.
This study examined how aging affects AICD gene expression in zebrafish. The researchers analyzed AICD RNA levels in the gut tissue of 5-, 11-, and 13-month old zebrafish using qPCR and found no significant difference, indicating that AICD expression is not altered during this period. They also found that changing the zebrafish housing conditions did not affect AICD levels. Future work will involve analyzing AICD and Tcf3a gene expression in 20-month old zebrafish to further study the effects of aging, requiring the isolation of B-cells from the zebrafish.
This document summarizes a presentation on characterizing extreme diversity in the human genome using a single haplotype genomic resource called CHM1. The presentation discusses how CHM1, which is a hydatidiform mole genome, provides a highly contiguous single haplotype representation of the genome that can help identify misassemblies in the current reference genome and regions with high genetic variation. It also describes how finishing additional diverse genomes and incorporating them into a population reference graph could help make the reference more representative of human genetic diversity.
- In a system where every somatic mutation could be identified (Tdt -/-), reversion of somatic mutations to germline eliminated autoreactivity in most clones, supporting that autoreactive clones arise from nonautoreactive precursors via somatic hypermutation.
- In an autoimmune mouse model lacking somatic hypermutation (AID deficiency), anti-nuclear responses were delayed and diminished, further supporting this view.
- IgV genes have high frequencies of AGY serine codons in CDRs that can readily mutate to arginine residues during somatic hypermutation. This suggests these genes are evolutionarily selected to facilitate the creation of autoreactive clones via somatic hypermutation.
1. Single-cell RNA sequencing was performed on hematopoietic stem cells isolated from myelodysplastic syndrome patients and normal individuals to characterize heterogeneity. Cells were collected before and after treatment with decitabine from responders and non-responders.
2. Differential expression analysis identified genes dysregulated in MDS compared to normal, including pathways involved in hematopoiesis. Clusters of patients were identified based on expression of hematopoietic stem cell signature genes.
3. The study aims to understand heterogeneity in MDS, factors influencing response to therapy, and disease progression by characterizing gene expression profiles at the single-cell level. This may help identify new therapeutic targets.
The CRISPR/Cas9 system has emerged as one of the leading tools for modifying genomes of organisms ranging from E. coli to humans. Additionally, the simple gene targeting mechanism of CRISPR technology has been modified and adapted to other applications that include gene regulation, detection of intercellular trafficking, and pathogen detection. With a wealth of methods for introducing Cas9 and gRNAs into cells, it can be challenging to decide where to start. In this presentation, Dr Adam Clore describes the CRISPR mechanism and some of the most prominent uses for CRISPR, along with methods where IDT technologies can assist scientists in designing, testing, and executing a variety of CRISPR-mediated experiments. For more informaton, visit: http://www.idtdna.com/crispr
KromaTiD's directional genomic hybridization (dGH) platform uses single-stranded probes to discover, detect, and diagnose structural variants like inversions and translocations at high resolution on a cell-by-cell basis. This complements next-generation sequencing and microarrays. dGH assays can find inherited, spontaneous, and induced mutations. PinPoint FISH assays then allow targeted detection of variants identified by dGH. KromaTiD offers both research services using its techniques and collaboration with customer labs.
Lessons learned from high throughput CRISPR targeting in human cell linesChris Thorne
In just a short period of time CRISPR-Cas9 technology has revolutionized the field of genome editing, and taken the scientific community by storm. Already our understanding of how best to apply this technology has advanced significantly and almost every week new publications appear showcasing its application in basic and translational research.
While CRISPR-Cas9 is applicable across many different cell types, we have found it particularly suited for genome editing in near-haploid human cell lines. This has allowed us to establish a robust pipeline for the inactivation of non-essential genes at unprecedented scale and efficiency.
We have now knocked out over 1500 human genes and have generated a resource that is, to the best of our knowledge, the largest collection of human knockout cell lines available, covering comprehensive subsets of genes clustered by biological pathway (e.g. the autophagy pathway, the JAK/STAT pathway) or by phylogenetic relationship (e.g. kinases, bromodomain-containing proteins).
In this talk we will discuss how, through more than 1500 genome editing experiments, we have started to unravel some of the general principles governing the use of CRISPR-Cas9 in mammalian cells. For example, we have analyzed the impact of variation in the guide RNA sequence on Cas9 cleavage efficiency and characterized the mutational signature arising from CRISPR-Cas9 cleavage.
We will also highlight (with examples) how these learnings are now being applied to introduce other genomic modifications in a high throughput manner, including chromosomal deletions, translocations, point mutations and endogenous gene tags.
This study examined how aging affects AICD gene expression in zebrafish. The researchers analyzed AICD RNA levels in the gut tissue of 5-, 11-, and 13-month old zebrafish using qPCR and found no significant difference, indicating that AICD expression is not altered during this period. They also found that changing the zebrafish housing conditions did not affect AICD levels. Future work will involve analyzing AICD and Tcf3a gene expression in 20-month old zebrafish to further study the effects of aging, requiring the isolation of B-cells from the zebrafish.
This document summarizes a presentation on characterizing extreme diversity in the human genome using a single haplotype genomic resource called CHM1. The presentation discusses how CHM1, which is a hydatidiform mole genome, provides a highly contiguous single haplotype representation of the genome that can help identify misassemblies in the current reference genome and regions with high genetic variation. It also describes how finishing additional diverse genomes and incorporating them into a population reference graph could help make the reference more representative of human genetic diversity.
- In a system where every somatic mutation could be identified (Tdt -/-), reversion of somatic mutations to germline eliminated autoreactivity in most clones, supporting that autoreactive clones arise from nonautoreactive precursors via somatic hypermutation.
- In an autoimmune mouse model lacking somatic hypermutation (AID deficiency), anti-nuclear responses were delayed and diminished, further supporting this view.
- IgV genes have high frequencies of AGY serine codons in CDRs that can readily mutate to arginine residues during somatic hypermutation. This suggests these genes are evolutionarily selected to facilitate the creation of autoreactive clones via somatic hypermutation.
In Vitro Characterization of a Novel Cis-acting Element (NCE) in the Cd4 Locus Yordan Penev
We have characterized a novel cis-acting regulatory element (NCE) in the Cd4 locus that exhibits developmental stage specificity in murine T cell lines. NCE functions as an enhancer in cell lines representing the intermediate and single positive developmental stages, but not in double positive stage cell lines. Transcription factor expression levels in the cell lines match expected developmental profiles, except for ThPok in one cell line. Initial experiments found no correlation between T cell receptor stimulation and NCE function. We are working to define the minimum functional sequence of NCE and identify transcription factors that bind it to understand how it regulates increasing Cd4 expression as thymocytes mature.
Presentation by Justin Zook at GRC/GIAB ASHG 2017 workshop "Getting the most from the reference assembly and reference materials" on benchmarks for indels and structural variants.
The document summarizes a study that used live cell imaging to visualize hepatitis C virus (HCV) entry into human liver cells. Key findings include:
1) HCV was labeled with fluorescent membrane dyes and found to move along actin stress fibers in an actin-dependent manner after internalization, suggesting clathrin-mediated endocytosis.
2) Inhibition of clathrin machinery or related host factors blocked HCV entry. Immunofluorescence showed HCV co-localizing with clathrin and early endosomes.
3) While tight junction proteins were thought to mediate HCV entry, live imaging found internalization occurring outside of tight junctions, indicating their role may be overstated.
4
ICMP MPS SNP Panel for Missing Persons - Michelle Peck et al.QIAGEN
Optimization and Performance of a Very Large MGS SNP Panel for Missing Persons, by Michelle Peck et al., International Commission on Mission Persons. Presented May 3, 2018, at the QIAGEN Investigator Forum, San Antonio, TX.
1. The document discusses variant calling from NGS data and prioritizing variants. It covers calling variants, identifying somatic mutations by comparing tumor and normal samples, and identifying inherited variants using trio analysis.
2. Key steps include calling variants, filtering, identifying somatic mutations as variants present in tumor but not normal, and identifying inherited variants by applying models of inheritance to family trio data.
3. Prioritization considers functional impact, population frequencies, and visual inspection to select candidates for follow up.
GENESIS™: Comprehensive genome editing - Translating genetic information into personalised medicines.
Horizon is the only source of rAAV expertise and is uniquely capable of exploiting multiple platforms: CRISPR, ZFNs and rAAV singularly or combined. Horizon’s scientists are experts at all forms of gene editing and so have the experience to help guide customers towards the approach that best suits their project
This document provides an overview of genome editing techniques such as CRISPR/Cas9 and rAAV and considerations for their use. It discusses how CRISPR/Cas9 and rAAV work to edit genomes and compares their advantages. Key factors for CRISPR gene editing are discussed such as gRNA design, donor design, and screening/validation approaches. The document also summarizes research optimizing CRISPR gene editing through improvements like testing different donor lengths and modifications. The goal is to translate genetic information into personalized medicines by leveraging tools like CRISPR and rAAV.
This document summarizes a project studying the CXCR4 co-receptor in CD4+ T cell normal and depleted sooty mangabeys. The project aims to sequence the CXCR4 gene in sooty mangabeys and compare it to human CXCR4 sequence. The hypothesis is that an amino acid difference in the V3 extracellular loop of sooty mangabey CXCR4 may make it more difficult for HIV to use as a co-receptor compared to humans. Blood samples were collected from normal and depleted CD4+ sooty mangabeys and CXCR4 was amplified by PCR and sequenced. Preliminary results found differences between sooty mangabey and human CXCR4 sequences that could impact HIV
Next Generation Sequencing and its Applications in Medical Research - Frances...Sri Ambati
The so-called “next-generation” sequencing (NGS) technologies allows us, in a short time and in parallel, to sequence massive amounts of DNA, overcoming the limitations of the original Sanger sequencing methods used to sequence the first human genome. NGS technologies have had an enormous impact on biomedical research within a short time frame. This talk will give an overview of these applications with specific examples from Mendelian genomics and cancer research. #h2ony
The document discusses the CRISPR/Cas9 system. It describes how CRISPR/Cas9 uses a Cas9 protein guided by a single guide RNA to recognize and cut target DNA. The system has three stages: adaptation, expression and processing of CRISPR RNA, and interference where the Cas9 protein complex cuts the target DNA. CRISPR/Cas9 can be engineered to act as a nuclease, nickase, or inactive dead Cas9 for gene regulation applications like activation or repression. It provides a gift from nature for precise genome editing and regulation.
Dr. Chris Lowe presented on Horizon Discovery's precision genome editing platform called GENESISTM. The presentation discussed optimizing GENESISTM by combining CRISPR and rAAV technologies to improve gene targeting efficiency. Custom cell line development services are offered to modify genes of interest in various cell lines for applications such as generating disease models and studying drug sensitivity. Key considerations for successful gene editing experiments include factors like gene/cell line selection, gRNA design/activity, donor design, screening/validation approaches. Case studies demonstrated applications of engineered cell lines.
This document summarizes a student project aimed at developing a gene therapy technique using CCR5 Δ32 mutation to potentially cure HIV/AIDS. The project involves collecting a blood sample from a participant with the CCR5 Δ32 mutation, purifying the DNA, inserting it into a vector, and transducing cells to integrate the modified gene and block HIV entry. The goal is to develop an easier gene therapy method that could cure HIV by reversing the virus's effects, as was seen in the case of Timothy Ray Brown.
Making genome edits in mammalian cellsChris Thorne
Looking at the kind of modifications that can be made in mammalian cells, and how at Horizon moving to a haploid model system has significantly improved efficiency of both editing and validation
This document discusses methods for detecting SARS-CoV-2, the virus that causes COVID-19. It first describes SARS-CoV-2 as being similar to but less pathogenic than SARS-CoV and using the same receptor. It then discusses using RT-PCR and RFLP tests to detect and differentiate SARS-CoV-2 from SARS-CoV. RT-PCR amplifies a specific DNA sequence for analysis, while RFLP detects polymorphisms between DNA sequences using restriction endonucleases. The general objective is to establish a simple method to detect SARS-CoV-2 and differentiate it from SARS-CoV. The document evaluates the sensitivity and specificity of the testing method.
This document summarizes a student research project that analyzed the frequency of the CCR5 Δ32 allele in a population in Northeastern Ohio. The students mapped primers for the CCR5 gene, developed a DNA collection and analysis protocol, and tested 50 samples from their population. Their results found that 45 samples were homozygous wild-type, 5 were heterozygous for the Δ32 mutation, and none were homozygous. They conclude that the Δ32 allele frequency in this population is 5%. Future plans include further testing at their college and using the Δ32 mutation for potential gene therapy.
This document summarizes a student research project that analyzed the frequency of the CCR5 Delta 32 allele in a population in Northeastern Ohio. The students mapped the CCR5 gene, developed a DNA collection and analysis protocol, and tested 50 samples. Their results found that 5 out of the 50 samples were heterozygous for the Delta 32 allele, indicating a gene frequency of 5% in the population. The students propose continuing their research and exploring using the Delta 32 mutation for potential gene therapy applications.
Recent breakthroughs in genome editing technology have led to a rapid adoption that parallels that seen with RNAi. And like RNAi, these methods are taking the scientific world by storm, with high profile publications in fields as diverse as HIV treatment, stem cell therapy, food crop modification and drug development to name but a few.
Critically, the endogenous modification of genes enables the study of their function in a physiological context. It also overcomes some of the artefacts that can result from established techniques such as transgenesis and RNAi, which have mislead researchers with false positives or negatives. Until recently however genome editing required considerable technical expertise, and consequently was a relatively niche pursuit.
In this talk we will look at how the latest developments in genome editing tools have changed this, with improvements in both ease-of-use and targeting efficiency, as well as a concomitant reduction in costs opening up these approaches to the wider scientific community.
Rapid adoption of the CRISPR/Cas9 system has for example led to a long list of organisms and tissues in which genetic changes have been made with high efficiency. Other technologies such as recombinant adeno-associated virus (rAAV) offer further precision, stimulating the cell’s high-fidelity DNA repair pathways to insert exogenous sequence with unrivalled specificity. Targeting efficiency can be improved still further by using the technologies in combination – genome cutting induced by CRISPR can significantly enhance homologous recombination mediated by rAAV.
Despite these rapid advances, some pitfalls remain, and so we’ll discuss some of the key considerations for avoiding these, ranging from simply picking the right tool for the job to designing an experiment that maximises chances of success.
Finally we’ll look at how genome editing is being applied to both basic and translational research, and in both a gene-specific and genome wide manner. For the study of disease associated genes and mutations scientists can now complement wide panels of tumour cells with genetically defined isogenic cell pairs identical in all but precise modifications in their gene of interest. The ease-of-design and efficiency of the CRISPR system is also being exploited for genome wide synthetic lethality screens, facilitating rapid drug target identification with significantly reduced risk of false negatives and off-target false positives. And again, further synergies are achieved when these approaches are combined to look for potential synthetic lethal targets in specific genomic contexts.
a brief description on the new emerging genome editing technology CRISPR-Cas9. this technique is making its place stronger and stronger day by day. and impossible things can be possible by this technique. and some main and famous names who discovered this technique.
DNA microarray is a technique that allows high-throughput analysis of gene expression. It involves depositing DNA fragments onto a glass slide and using fluorescent probes made from sample RNA to detect expression levels of thousands of genes simultaneously. The document discusses the basic principles and steps of DNA microarray, including sample preparation, hybridization, image analysis and data normalization. It also compares different microarray fabrication technologies and platforms, and discusses quality control considerations and limitations of the technique.
Literature mining: what is it, and should I care?Lars Juhl Jensen
The document discusses literature mining and natural language processing techniques for extracting information from scientific papers. It describes steps in an NLP pipeline including information retrieval to find relevant papers, entity recognition to identify substances, and information extraction to formalize facts. It also briefly acknowledges databases and tools used, and references a movie.
In Vitro Characterization of a Novel Cis-acting Element (NCE) in the Cd4 Locus Yordan Penev
We have characterized a novel cis-acting regulatory element (NCE) in the Cd4 locus that exhibits developmental stage specificity in murine T cell lines. NCE functions as an enhancer in cell lines representing the intermediate and single positive developmental stages, but not in double positive stage cell lines. Transcription factor expression levels in the cell lines match expected developmental profiles, except for ThPok in one cell line. Initial experiments found no correlation between T cell receptor stimulation and NCE function. We are working to define the minimum functional sequence of NCE and identify transcription factors that bind it to understand how it regulates increasing Cd4 expression as thymocytes mature.
Presentation by Justin Zook at GRC/GIAB ASHG 2017 workshop "Getting the most from the reference assembly and reference materials" on benchmarks for indels and structural variants.
The document summarizes a study that used live cell imaging to visualize hepatitis C virus (HCV) entry into human liver cells. Key findings include:
1) HCV was labeled with fluorescent membrane dyes and found to move along actin stress fibers in an actin-dependent manner after internalization, suggesting clathrin-mediated endocytosis.
2) Inhibition of clathrin machinery or related host factors blocked HCV entry. Immunofluorescence showed HCV co-localizing with clathrin and early endosomes.
3) While tight junction proteins were thought to mediate HCV entry, live imaging found internalization occurring outside of tight junctions, indicating their role may be overstated.
4
ICMP MPS SNP Panel for Missing Persons - Michelle Peck et al.QIAGEN
Optimization and Performance of a Very Large MGS SNP Panel for Missing Persons, by Michelle Peck et al., International Commission on Mission Persons. Presented May 3, 2018, at the QIAGEN Investigator Forum, San Antonio, TX.
1. The document discusses variant calling from NGS data and prioritizing variants. It covers calling variants, identifying somatic mutations by comparing tumor and normal samples, and identifying inherited variants using trio analysis.
2. Key steps include calling variants, filtering, identifying somatic mutations as variants present in tumor but not normal, and identifying inherited variants by applying models of inheritance to family trio data.
3. Prioritization considers functional impact, population frequencies, and visual inspection to select candidates for follow up.
GENESIS™: Comprehensive genome editing - Translating genetic information into personalised medicines.
Horizon is the only source of rAAV expertise and is uniquely capable of exploiting multiple platforms: CRISPR, ZFNs and rAAV singularly or combined. Horizon’s scientists are experts at all forms of gene editing and so have the experience to help guide customers towards the approach that best suits their project
This document provides an overview of genome editing techniques such as CRISPR/Cas9 and rAAV and considerations for their use. It discusses how CRISPR/Cas9 and rAAV work to edit genomes and compares their advantages. Key factors for CRISPR gene editing are discussed such as gRNA design, donor design, and screening/validation approaches. The document also summarizes research optimizing CRISPR gene editing through improvements like testing different donor lengths and modifications. The goal is to translate genetic information into personalized medicines by leveraging tools like CRISPR and rAAV.
This document summarizes a project studying the CXCR4 co-receptor in CD4+ T cell normal and depleted sooty mangabeys. The project aims to sequence the CXCR4 gene in sooty mangabeys and compare it to human CXCR4 sequence. The hypothesis is that an amino acid difference in the V3 extracellular loop of sooty mangabey CXCR4 may make it more difficult for HIV to use as a co-receptor compared to humans. Blood samples were collected from normal and depleted CD4+ sooty mangabeys and CXCR4 was amplified by PCR and sequenced. Preliminary results found differences between sooty mangabey and human CXCR4 sequences that could impact HIV
Next Generation Sequencing and its Applications in Medical Research - Frances...Sri Ambati
The so-called “next-generation” sequencing (NGS) technologies allows us, in a short time and in parallel, to sequence massive amounts of DNA, overcoming the limitations of the original Sanger sequencing methods used to sequence the first human genome. NGS technologies have had an enormous impact on biomedical research within a short time frame. This talk will give an overview of these applications with specific examples from Mendelian genomics and cancer research. #h2ony
The document discusses the CRISPR/Cas9 system. It describes how CRISPR/Cas9 uses a Cas9 protein guided by a single guide RNA to recognize and cut target DNA. The system has three stages: adaptation, expression and processing of CRISPR RNA, and interference where the Cas9 protein complex cuts the target DNA. CRISPR/Cas9 can be engineered to act as a nuclease, nickase, or inactive dead Cas9 for gene regulation applications like activation or repression. It provides a gift from nature for precise genome editing and regulation.
Dr. Chris Lowe presented on Horizon Discovery's precision genome editing platform called GENESISTM. The presentation discussed optimizing GENESISTM by combining CRISPR and rAAV technologies to improve gene targeting efficiency. Custom cell line development services are offered to modify genes of interest in various cell lines for applications such as generating disease models and studying drug sensitivity. Key considerations for successful gene editing experiments include factors like gene/cell line selection, gRNA design/activity, donor design, screening/validation approaches. Case studies demonstrated applications of engineered cell lines.
This document summarizes a student project aimed at developing a gene therapy technique using CCR5 Δ32 mutation to potentially cure HIV/AIDS. The project involves collecting a blood sample from a participant with the CCR5 Δ32 mutation, purifying the DNA, inserting it into a vector, and transducing cells to integrate the modified gene and block HIV entry. The goal is to develop an easier gene therapy method that could cure HIV by reversing the virus's effects, as was seen in the case of Timothy Ray Brown.
Making genome edits in mammalian cellsChris Thorne
Looking at the kind of modifications that can be made in mammalian cells, and how at Horizon moving to a haploid model system has significantly improved efficiency of both editing and validation
This document discusses methods for detecting SARS-CoV-2, the virus that causes COVID-19. It first describes SARS-CoV-2 as being similar to but less pathogenic than SARS-CoV and using the same receptor. It then discusses using RT-PCR and RFLP tests to detect and differentiate SARS-CoV-2 from SARS-CoV. RT-PCR amplifies a specific DNA sequence for analysis, while RFLP detects polymorphisms between DNA sequences using restriction endonucleases. The general objective is to establish a simple method to detect SARS-CoV-2 and differentiate it from SARS-CoV. The document evaluates the sensitivity and specificity of the testing method.
This document summarizes a student research project that analyzed the frequency of the CCR5 Δ32 allele in a population in Northeastern Ohio. The students mapped primers for the CCR5 gene, developed a DNA collection and analysis protocol, and tested 50 samples from their population. Their results found that 45 samples were homozygous wild-type, 5 were heterozygous for the Δ32 mutation, and none were homozygous. They conclude that the Δ32 allele frequency in this population is 5%. Future plans include further testing at their college and using the Δ32 mutation for potential gene therapy.
This document summarizes a student research project that analyzed the frequency of the CCR5 Delta 32 allele in a population in Northeastern Ohio. The students mapped the CCR5 gene, developed a DNA collection and analysis protocol, and tested 50 samples. Their results found that 5 out of the 50 samples were heterozygous for the Delta 32 allele, indicating a gene frequency of 5% in the population. The students propose continuing their research and exploring using the Delta 32 mutation for potential gene therapy applications.
Recent breakthroughs in genome editing technology have led to a rapid adoption that parallels that seen with RNAi. And like RNAi, these methods are taking the scientific world by storm, with high profile publications in fields as diverse as HIV treatment, stem cell therapy, food crop modification and drug development to name but a few.
Critically, the endogenous modification of genes enables the study of their function in a physiological context. It also overcomes some of the artefacts that can result from established techniques such as transgenesis and RNAi, which have mislead researchers with false positives or negatives. Until recently however genome editing required considerable technical expertise, and consequently was a relatively niche pursuit.
In this talk we will look at how the latest developments in genome editing tools have changed this, with improvements in both ease-of-use and targeting efficiency, as well as a concomitant reduction in costs opening up these approaches to the wider scientific community.
Rapid adoption of the CRISPR/Cas9 system has for example led to a long list of organisms and tissues in which genetic changes have been made with high efficiency. Other technologies such as recombinant adeno-associated virus (rAAV) offer further precision, stimulating the cell’s high-fidelity DNA repair pathways to insert exogenous sequence with unrivalled specificity. Targeting efficiency can be improved still further by using the technologies in combination – genome cutting induced by CRISPR can significantly enhance homologous recombination mediated by rAAV.
Despite these rapid advances, some pitfalls remain, and so we’ll discuss some of the key considerations for avoiding these, ranging from simply picking the right tool for the job to designing an experiment that maximises chances of success.
Finally we’ll look at how genome editing is being applied to both basic and translational research, and in both a gene-specific and genome wide manner. For the study of disease associated genes and mutations scientists can now complement wide panels of tumour cells with genetically defined isogenic cell pairs identical in all but precise modifications in their gene of interest. The ease-of-design and efficiency of the CRISPR system is also being exploited for genome wide synthetic lethality screens, facilitating rapid drug target identification with significantly reduced risk of false negatives and off-target false positives. And again, further synergies are achieved when these approaches are combined to look for potential synthetic lethal targets in specific genomic contexts.
a brief description on the new emerging genome editing technology CRISPR-Cas9. this technique is making its place stronger and stronger day by day. and impossible things can be possible by this technique. and some main and famous names who discovered this technique.
DNA microarray is a technique that allows high-throughput analysis of gene expression. It involves depositing DNA fragments onto a glass slide and using fluorescent probes made from sample RNA to detect expression levels of thousands of genes simultaneously. The document discusses the basic principles and steps of DNA microarray, including sample preparation, hybridization, image analysis and data normalization. It also compares different microarray fabrication technologies and platforms, and discusses quality control considerations and limitations of the technique.
Literature mining: what is it, and should I care?Lars Juhl Jensen
The document discusses literature mining and natural language processing techniques for extracting information from scientific papers. It describes steps in an NLP pipeline including information retrieval to find relevant papers, entity recognition to identify substances, and information extraction to formalize facts. It also briefly acknowledges databases and tools used, and references a movie.
This document discusses natural language processing and text mining techniques for biomedical literature and electronic health records. It describes named entity recognition to identify concepts like genes and proteins, relation extraction to find interactions between entities, and information extraction to formalize stated facts. It also discusses integrating extracted information with structured databases and visualizing relationships through web interfaces. Medical text mining can apply these techniques to clinical notes to identify diseases, drugs, adverse events and more for applications like comorbidity analysis, patient stratification, and pharmacovigilance.
Text mining techniques can be used to extract information and insights from the exponential growth of scientific literature. Key techniques include information retrieval to find relevant papers, named entity recognition to identify concepts, and information extraction to formalize facts. These techniques can be evaluated using benchmarking against manually annotated corpora, though creating such resources requires significant effort and the pragmatic approach of inspecting text mining outputs is much less work.
This document discusses various techniques in applied text mining, including named entity recognition, information extraction, and text/data integration. It covers extracting facts from text using natural language processing approaches like part-of-speech tagging and semantic tagging. It also discusses more pragmatic approaches using techniques like co-mentioning and guilt by association. The goal is to formalize biological facts and integrate text-derived information with databases of experimental data and computational predictions to build more comprehensive resources. Challenges include dealing with different data formats, identifiers, and quality across the many available databases.
This document discusses text mining and data integration techniques used to extract information from biomedical literature and databases. It describes named entity recognition to identify concepts, co-mentioning analysis to find associations between entities, and using these methods along with experimental data and predictions to build integrated networks of genes and proteins and their relationships. These networks are made accessible through web resources that unify data from various sources under common identifiers and provide visualization and programmatic access.
This document discusses mining literature and medical records using text mining techniques. It summarizes that text mining can be used to extract relevant information from large collections of scientific papers and medical records by using techniques like named entity recognition to identify concepts, information extraction to formalize stated facts, and analyzing co-mentioning of entities to find relationships. Challenges include the unstructured nature of medical records, differences between languages and formats, and privacy concerns when using patient health information. When applied carefully, text mining of literature and medical records can help identify new relationships and insights not captured in existing curated databases or help with medical research questions.
Text mining can summarize scientific documents in 3 sentences or less by identifying key entities and relationships. It recognizes concepts like genes, proteins, diseases and extracts facts from text. This extracted information can then be integrated with other data to create more useful resources and provide novel insights through augmented browsing and analysis. Text mining aims to make navigating vast amounts of scientific literature simpler and less boring.
The document discusses text mining and natural language processing techniques for extracting information from scientific documents, including information retrieval, entity recognition, and information extraction. It provides examples of identifying entities like genes and proteins, and extracting relationships between entities, such as regulatory interactions, from text. The techniques discussed aim to formalize facts and biological knowledge from unstructured text into a structured database for further analysis.
This document discusses biomedical text mining techniques used to extract information from scientific papers. It covers named entity recognition to identify concepts like proteins, chemicals and diseases. It also discusses information extraction to formalize facts stated in text, such as interactions between biological components. Techniques include co-mentioning analysis and natural language processing and tools have been applied to large text corpora to aid discovery.
Biomedical literature mining (and why we really need open access)Lars Juhl Jensen
The 28th IATUL annual conference: Global Access to Science - Scientific Publishing for the Future, Royal Institute of Technology (KTH), Stockholm, Sweden, June 11-14, 2007
This document discusses various methodologies for extracting information from biological literature, including information retrieval, entity recognition, information extraction, and text/data mining. It provides an overview of different approaches like using co-occurrence, natural language processing, and machine learning methods. It also discusses challenges like integrating text with other data types and dealing with issues like ambiguity. Examples of existing text mining tools and their potential applications are also described.
Text mining for protein and small molecule relationsLars Juhl Jensen
The document discusses using text mining to identify relationships between proteins and small molecules mentioned in biomedical documents. It describes techniques for entity recognition and identification, as well as methods for extracting relationships between entities using co-occurrence analysis and natural language processing. Examples are provided to illustrate how relationships can be identified between proteins mentioned in a sample text passage.
The document discusses various techniques for literature mining and systems biology including information retrieval, entity recognition, information extraction, text mining, and integration of text and biological data. It provides examples and status of different methods, from established techniques for information retrieval, entity recognition, and simple information extraction to improving advanced natural language processing-based information extraction and methods for text mining and integration of text and data.
Biological literature mining - from information retrieval to biological disco...Lars Juhl Jensen
14th International Conference on Intelligent Systems for Molecular Biology, Tutorial, Fortaleza Conference Center, Fortaleza, Brazil, August 6-10, 2006
From Advanced Queries to Algorithms and Graph-Based ML: Tackling Diabetes wit...Neo4j
This document describes 3 use cases for a pharmaceutical knowledge graph created by the Data and Knowledge Management team at the German Center for Neurodegenerative Diseases (DZD). The knowledge graph connects heterogeneous and unstructured data using a graph database. The 3 use cases are: 1) Mapping identifiers to handle molecular entities, 2) Finding connected information by querying relationships, and 3) Annotating and enriching text with natural language processing and ontologies. The knowledge graph allows for advanced queries, graph algorithms, and machine learning techniques to gain new insights.
Similar to Computational approaches to cell cycle analysis: Current research topics (those I am allowed to talk about) (20)
One tagger, many uses: Illustrating the power of dictionary-based named entit...Lars Juhl Jensen
This document summarizes a Twitter thread discussing the uses of a dictionary-based named entity recognition tool called Tagger. Tagger can recognize genes, proteins, diseases and other biomedical entities. It is open source, runs quickly processing over 1000 abstracts per second, and achieves 70-80% recall and 80-90% precision. Tagger has been applied to tasks like identifying drug-disease associations, adverse drug events, and protein-protein interactions. It is available as a Docker container or web service.
One tagger, many uses: Simple text-mining strategies for biomedicineLars Juhl Jensen
The document summarizes a text mining tool called a tagger that can be used for named entity recognition in biomedical texts. It recognizes genes, proteins, chemicals, diseases, and other entities. The tagger is open source, runs quickly at over 1000 abstracts per second, and has 70-80% recall and 80-90% precision. It comes with Python and Docker implementations and can be accessed via a web service. It is useful for tasks like extracting functional associations from literature and electronic health records.
This document describes Extract 2.0, a text-mining tool that can assist with interactive annotation of documents. It uses dictionary-based tagging to identify relevant entities like genes and diseases. It achieves 70-80% recall and 80-90% precision on entity extraction and was evaluated in BioCreative challenges where it received positive feedback from curators. The tool is open source and available as a web service or Python wrapper.
Network visualization: A crash course on using CytoscapeLars Juhl Jensen
This document discusses using Cytoscape, a network analysis tool, to import and visualize networks from STRING and STITCH databases. It provides three examples of networks created from literature and disease queries, demonstrating how to import networks and tables, apply node attributes and visual styles, perform enrichment analysis, and more.
STRING & STITCH: Network integration of heterogeneous dataLars Juhl Jensen
The document discusses STRING and STITCH, two online databases that integrate data on protein-protein interactions, pathways, and functional associations from various sources. STRING collects data on over 9.6 million proteins and 430 thousand chemicals from sources like text mining, experimental assays, and co-expression analyses. It aims to provide a comprehensive global view of known and predicted protein associations. STITCH also integrates interaction data but focuses more on chemical-protein interactions. Both databases provide user-friendly web interfaces for browsing and visualizing interaction networks.
Biomedical text mining: Automatic processing of unstructured textLars Juhl Jensen
1) Lars Juhl Jensen discusses biomedical text mining and automatic processing of unstructured text such as patent literature, grant proposals, FDA product labels, and electronic medical records.
2) Named entity recognition is used to identify genes/proteins, chemical compounds, diseases, and other entities in text through comprehensive dictionaries and flexible matching rules that account for variations.
3) Relation extraction uses natural language processing techniques like part-of-speech tagging and sentence parsing along with manually crafted rules and machine learning to identify implicit relations between entities in text such as transcription factor targets, kinase substrates, and protein-protein interactions.
Medical network analysis: Linking diseases and genes through data and text mi...Lars Juhl Jensen
The document summarizes the work of Lars Juhl Jensen and others on medical network analysis and linking diseases and genes through data and text mining of electronic health records. It discusses how they have used Danish national health registries containing data on over 6 million patients and 119 million diagnoses over 14 years to study disease trajectories and comorbidities. It also describes how they have developed methods to integrate data from various sources to generate networks linking diseases and genes.
Network Biology: A crash course on STRING and CytoscapeLars Juhl Jensen
This document provides an overview of STRING, a protein-protein association database, and Cytoscape, a network visualization tool. It describes how STRING contains functional associations between proteins derived from genomic context, co-expression and curated databases. Cytoscape can import STRING networks and external data to map onto nodes. It offers visualization of networks through layouts and attributes, and analysis through clustering, selection filters and enrichment. The document recommends using these tools together to explore protein association networks.
This document discusses different approaches to visualizing cellular networks and the molecular interactions between proteins. It notes that there are many different types of data that could be shown, such as protein names, functions, localization, expression, modifications, and interaction types. However, it is impossible to show all this information at once. The document recommends using different visualizations like force-directed layouts to distribute proteins in 2D or lining up interactions in 1D. It acknowledges open challenges like showing time-course data and modification sites. In the end, the document thanks several researchers who have contributed to mapping and visualizing cellular networks.
Cellular Network Biology: Large-scale integration of data and textLars Juhl Jensen
The document discusses various community resources and software tools for integrating large-scale data and text, including STRING for protein networks, STITCH for chemical networks, COMPARTMENTS for subcellular localization, TISSUES for tissue expression, and DISEASES for disease associations. It provides an overview of text mining techniques used to extract information from literature to build networks in these resources. The presenter demonstrates the Cytoscape App which can import and analyze networks from STRING, perform queries, and analyze subcellular localization, tissue expression, and disease enrichment.
Statistics on big biomedical data: Methods and pitfalls when analyzing high-t...Lars Juhl Jensen
This document discusses statistical methods for analyzing high-throughput biomedical screens and common pitfalls. It introduces several statistical tests such as t-tests, ANOVA, Fisher's exact test, and the Mann-Whitney U test. It also discusses challenges like multiple testing, resampling techniques, and biases that can occur like studiedness bias and abundance bias in big data analyses. Controlling false discovery rates and considering effect sizes are recommended over solely relying on p-values to determine biological significance.
STRING & related databases: Large-scale integration of heterogeneous dataLars Juhl Jensen
The document discusses the STRING database, which integrates heterogeneous biological data to generate association networks for proteins. It describes how STRING collects and connects curated knowledge, experimental data, and predicted interactions from genomic context, co-expression and text mining. The document also outlines exercises for users to explore protein-protein associations in STRING and related databases that integrate data on subcellular localization, tissue expression, and disease associations.
Tagger: Rapid dictionary-based named entity recognitionLars Juhl Jensen
Tagger is a named entity recognition tool that can process over 1000 abstracts per second using a dictionary-based approach. It achieves 70-80% recall and 80-90% precision using comprehensive dictionaries, expansion rules, and a curated blacklist to identify entity types like genes, proteins, chemicals, and diseases. The tool has a C++ engine, is inherently thread-safe, and includes interactive annotation, Python wrappers, and a REST API.
Network Biology: Large-scale integration of data and textLars Juhl Jensen
Lars Juhl Jensen leads a group that conducts large-scale integration of biological and medical data using proteomics, text mining, and medical data mining. The group develops protein interaction networks, disease networks, and association networks. They collaborate internationally on projects involving over 9.6 million proteins and 2000 genomes. The group works to integrate data from many sources in different formats to build comprehensive networks and knowledgebases, and also mines biomedical text to link genes and proteins with diseases.
Medical text mining: Linking diseases, drugs, and adverse reactionsLars Juhl Jensen
This document discusses medical text mining and linking diseases, drugs, and adverse reactions. It describes using text mining on clinical narratives in Danish to recognize named entities like drugs and diseases, identify relationships between them like adverse drug reactions, and discover new ADRs. The goal is to generate structured data on topics like comorbidities, diagnosis trajectories, and reimbursement to supplement limited structured data and help busy doctors by analyzing large amounts of unstructured text.
Network biology: Large-scale integration of data and textLars Juhl Jensen
The document discusses network biology and large-scale data integration. It describes protein-protein interaction networks like STRING that integrate data from curated knowledge, experiments, and predictions. It provides exercises to explore the human insulin receptor (INSR) in STRING, examining the types of evidence that support its interaction with IRS1. It also introduces other integrated networks like STITCH for chemicals and COMPARTMENTS for subcellular localization. Natural language processing techniques like named entity recognition, information extraction, and semantic tagging are used to integrate text data from the literature into these interaction networks.
Medical data and text mining: Linking diseases, drugs, and adverse reactionsLars Juhl Jensen
This document discusses medical data and text mining to link diseases, drugs, and adverse reactions. It describes using structured data from Danish central registries and unstructured data from hospital electronic health records. Named entity recognition is used to extract diseases, drugs, and adverse reactions from free text clinical notes written in Danish. Hand-crafted rules are developed to identify relationships between extracted entities like adverse drug reactions. This allows estimating frequencies of known adverse drug reactions and discovering new adverse drug reactions by analyzing diagnosis trajectories and medication information.
This document discusses cellular network biology and summarizes several key papers on topics like proteome analysis using mass spectrometry, integrating protein network and experimental data, challenges with different biological databases having varying formats and quality, and using natural language processing techniques like named entity recognition and relation extraction to analyze medical text for information like diagnosis trajectories and adverse drug reactions.
Network biology: Large-scale integration of data and textLars Juhl Jensen
This document discusses natural language processing (NLP) techniques for extracting information from biomedical literature and integrating it with network and interaction data. It describes how NLP is used to identify entities like genes and proteins, extract relationships between entities, and integrate this text-mined information with existing interaction networks from databases like STRING to expand knowledge of protein interactions, complexes, pathways and associations with diseases. The document provides examples of using NLP analysis on sentences and the STRING and Tissues databases to explore tissue specificity and disease relationships for insulin and the insulin receptor.
The document discusses three parts of biomarker bioinformatics: data integration from multiple databases, text mining of scientific literature, and using that integrated data to prioritize biomarker candidates. It describes combining data on 9.6 million proteins from curated databases, using text mining to extract named entities from over 10,000 papers, and then using network and heat diffusion approaches to rank candidates based on evidence in the integrated data. The goal is to help identify new biomarker candidates from large amounts of biological data.
Communications Mining Series - Zero to Hero - Session 1DianaGray10
This session provides introduction to UiPath Communication Mining, importance and platform overview. You will acquire a good understand of the phases in Communication Mining as we go over the platform with you. Topics covered:
• Communication Mining Overview
• Why is it important?
• How can it help today’s business and the benefits
• Phases in Communication Mining
• Demo on Platform overview
• Q/A
Observability Concepts EVERY Developer Should Know -- DeveloperWeek Europe.pdfPaige Cruz
Monitoring and observability aren’t traditionally found in software curriculums and many of us cobble this knowledge together from whatever vendor or ecosystem we were first introduced to and whatever is a part of your current company’s observability stack.
While the dev and ops silo continues to crumble….many organizations still relegate monitoring & observability as the purview of ops, infra and SRE teams. This is a mistake - achieving a highly observable system requires collaboration up and down the stack.
I, a former op, would like to extend an invitation to all application developers to join the observability party will share these foundational concepts to build on:
GraphRAG for Life Science to increase LLM accuracyTomaz Bratanic
GraphRAG for life science domain, where you retriever information from biomedical knowledge graphs using LLMs to increase the accuracy and performance of generated answers
Let's Integrate MuleSoft RPA, COMPOSER, APM with AWS IDP along with Slackshyamraj55
Discover the seamless integration of RPA (Robotic Process Automation), COMPOSER, and APM with AWS IDP enhanced with Slack notifications. Explore how these technologies converge to streamline workflows, optimize performance, and ensure secure access, all while leveraging the power of AWS IDP and real-time communication via Slack notifications.
Climate Impact of Software Testing at Nordic Testing DaysKari Kakkonen
My slides at Nordic Testing Days 6.6.2024
Climate impact / sustainability of software testing discussed on the talk. ICT and testing must carry their part of global responsibility to help with the climat warming. We can minimize the carbon footprint but we can also have a carbon handprint, a positive impact on the climate. Quality characteristics can be added with sustainability, and then measured continuously. Test environments can be used less, and in smaller scale and on demand. Test techniques can be used in optimizing or minimizing number of tests. Test automation can be used to speed up testing.
Goodbye Windows 11: Make Way for Nitrux Linux 3.5.0!SOFTTECHHUB
As the digital landscape continually evolves, operating systems play a critical role in shaping user experiences and productivity. The launch of Nitrux Linux 3.5.0 marks a significant milestone, offering a robust alternative to traditional systems such as Windows 11. This article delves into the essence of Nitrux Linux 3.5.0, exploring its unique features, advantages, and how it stands as a compelling choice for both casual users and tech enthusiasts.
GraphSummit Singapore | The Future of Agility: Supercharging Digital Transfor...Neo4j
Leonard Jayamohan, Partner & Generative AI Lead, Deloitte
This keynote will reveal how Deloitte leverages Neo4j’s graph power for groundbreaking digital twin solutions, achieving a staggering 100x performance boost. Discover the essential role knowledge graphs play in successful generative AI implementations. Plus, get an exclusive look at an innovative Neo4j + Generative AI solution Deloitte is developing in-house.
In his public lecture, Christian Timmerer provides insights into the fascinating history of video streaming, starting from its humble beginnings before YouTube to the groundbreaking technologies that now dominate platforms like Netflix and ORF ON. Timmerer also presents provocative contributions of his own that have significantly influenced the industry. He concludes by looking at future challenges and invites the audience to join in a discussion.
Why You Should Replace Windows 11 with Nitrux Linux 3.5.0 for enhanced perfor...SOFTTECHHUB
The choice of an operating system plays a pivotal role in shaping our computing experience. For decades, Microsoft's Windows has dominated the market, offering a familiar and widely adopted platform for personal and professional use. However, as technological advancements continue to push the boundaries of innovation, alternative operating systems have emerged, challenging the status quo and offering users a fresh perspective on computing.
One such alternative that has garnered significant attention and acclaim is Nitrux Linux 3.5.0, a sleek, powerful, and user-friendly Linux distribution that promises to redefine the way we interact with our devices. With its focus on performance, security, and customization, Nitrux Linux presents a compelling case for those seeking to break free from the constraints of proprietary software and embrace the freedom and flexibility of open-source computing.
Infrastructure Challenges in Scaling RAG with Custom AI modelsZilliz
Building Retrieval-Augmented Generation (RAG) systems with open-source and custom AI models is a complex task. This talk explores the challenges in productionizing RAG systems, including retrieval performance, response synthesis, and evaluation. We’ll discuss how to leverage open-source models like text embeddings, language models, and custom fine-tuned models to enhance RAG performance. Additionally, we’ll cover how BentoML can help orchestrate and scale these AI components efficiently, ensuring seamless deployment and management of RAG systems in the cloud.
In the rapidly evolving landscape of technologies, XML continues to play a vital role in structuring, storing, and transporting data across diverse systems. The recent advancements in artificial intelligence (AI) present new methodologies for enhancing XML development workflows, introducing efficiency, automation, and intelligent capabilities. This presentation will outline the scope and perspective of utilizing AI in XML development. The potential benefits and the possible pitfalls will be highlighted, providing a balanced view of the subject.
We will explore the capabilities of AI in understanding XML markup languages and autonomously creating structured XML content. Additionally, we will examine the capacity of AI to enrich plain text with appropriate XML markup. Practical examples and methodological guidelines will be provided to elucidate how AI can be effectively prompted to interpret and generate accurate XML markup.
Further emphasis will be placed on the role of AI in developing XSLT, or schemas such as XSD and Schematron. We will address the techniques and strategies adopted to create prompts for generating code, explaining code, or refactoring the code, and the results achieved.
The discussion will extend to how AI can be used to transform XML content. In particular, the focus will be on the use of AI XPath extension functions in XSLT, Schematron, Schematron Quick Fixes, or for XML content refactoring.
The presentation aims to deliver a comprehensive overview of AI usage in XML development, providing attendees with the necessary knowledge to make informed decisions. Whether you’re at the early stages of adopting AI or considering integrating it in advanced XML development, this presentation will cover all levels of expertise.
By highlighting the potential advantages and challenges of integrating AI with XML development tools and languages, the presentation seeks to inspire thoughtful conversation around the future of XML development. We’ll not only delve into the technical aspects of AI-powered XML development but also discuss practical implications and possible future directions.
UiPath Test Automation using UiPath Test Suite series, part 6DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 6. In this session, we will cover Test Automation with generative AI and Open AI.
UiPath Test Automation with generative AI and Open AI webinar offers an in-depth exploration of leveraging cutting-edge technologies for test automation within the UiPath platform. Attendees will delve into the integration of generative AI, a test automation solution, with Open AI advanced natural language processing capabilities.
Throughout the session, participants will discover how this synergy empowers testers to automate repetitive tasks, enhance testing accuracy, and expedite the software testing life cycle. Topics covered include the seamless integration process, practical use cases, and the benefits of harnessing AI-driven automation for UiPath testing initiatives. By attending this webinar, testers, and automation professionals can gain valuable insights into harnessing the power of AI to optimize their test automation workflows within the UiPath ecosystem, ultimately driving efficiency and quality in software development processes.
What will you get from this session?
1. Insights into integrating generative AI.
2. Understanding how this integration enhances test automation within the UiPath platform
3. Practical demonstrations
4. Exploration of real-world use cases illustrating the benefits of AI-driven test automation for UiPath
Topics covered:
What is generative AI
Test Automation with generative AI and Open AI.
UiPath integration with generative AI
Speaker:
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
Removing Uninteresting Bytes in Software FuzzingAftab Hussain
Imagine a world where software fuzzing, the process of mutating bytes in test seeds to uncover hidden and erroneous program behaviors, becomes faster and more effective. A lot depends on the initial seeds, which can significantly dictate the trajectory of a fuzzing campaign, particularly in terms of how long it takes to uncover interesting behaviour in your code. We introduce DIAR, a technique designed to speedup fuzzing campaigns by pinpointing and eliminating those uninteresting bytes in the seeds. Picture this: instead of wasting valuable resources on meaningless mutations in large, bloated seeds, DIAR removes the unnecessary bytes, streamlining the entire process.
In this work, we equipped AFL, a popular fuzzer, with DIAR and examined two critical Linux libraries -- Libxml's xmllint, a tool for parsing xml documents, and Binutil's readelf, an essential debugging and security analysis command-line tool used to display detailed information about ELF (Executable and Linkable Format). Our preliminary results show that AFL+DIAR does not only discover new paths more quickly but also achieves higher coverage overall. This work thus showcases how starting with lean and optimized seeds can lead to faster, more comprehensive fuzzing campaigns -- and DIAR helps you find such seeds.
- These are slides of the talk given at IEEE International Conference on Software Testing Verification and Validation Workshop, ICSTW 2022.
Unlock the Future of Search with MongoDB Atlas_ Vector Search Unleashed.pdfMalak Abu Hammad
Discover how MongoDB Atlas and vector search technology can revolutionize your application's search capabilities. This comprehensive presentation covers:
* What is Vector Search?
* Importance and benefits of vector search
* Practical use cases across various industries
* Step-by-step implementation guide
* Live demos with code snippets
* Enhancing LLM capabilities with vector search
* Best practices and optimization strategies
Perfect for developers, AI enthusiasts, and tech leaders. Learn how to leverage MongoDB Atlas to deliver highly relevant, context-aware search results, transforming your data retrieval process. Stay ahead in tech innovation and maximize the potential of your applications.
#MongoDB #VectorSearch #AI #SemanticSearch #TechInnovation #DataScience #LLM #MachineLearning #SearchTechnology
19. Mitotic cyclin (Clb2)-bound Cdc28 (Cdk1 homolog) directly phosphorylated Swe1 and this modification served as a priming step to promote subsequent Cdc5-dependent Swe1 hyperphosphorylation and degradation
23. Mitotic cyclin ( Clb2 )-bound Cdc28 (Cdk1 homolog) directly phosphorylated Swe1 and this modification served as a priming step to promote subsequent Cdc5 -dependent Swe1 hyperphosphorylation and degradation
43. Mitotic cyclin ( Clb2 )-bound Cdc28 (Cdk1 homolog) directly phosphorylated Swe1 and this modification served as a priming step to promote subsequent Cdc5 -dependent Swe1 hyperphosphorylation and degradation