This document provides information about bioinformatics resources including databases of nucleotide and protein sequences. It discusses flat file databases like GenBank that store sequence data in plain text files and relational databases that improve data organization. Examples of popular biological databases are described, such as GenBank, EMBL, and DDBJ for nucleotide sequences and Swiss-Prot and TrEMBL for protein sequences. The document also covers sequence file formats, web tools for querying databases, and trace files used in sequence assembly.
Course: Bioinformatics for Biomedical Research (2014).
Session: 4.1- Introduction to RNA-seq and RNA-seq Data Analysis.
Statistics and Bioinformatisc Unit (UEB) & High Technology Unit (UAT) from Vall d'Hebron Research Institute (www.vhir.org), Barcelona.
This document provides an overview of RNA-seq and its applications. It discusses key aspects of RNA-seq including transcriptome profiling, alignment, quantification, differential expression analysis, clustering and visualization. It also covers experimental design considerations and highlights some commonly used tools and software. The document is a comprehensive guide that describes the RNA-seq workflow and analysis from start to finish.
University of Manchester Symposium 2012: Extraction and Representation of in ...geraintduck
This document describes research extracting and analyzing biological methods mentioned in the scientific literature. It developed bioNerDS, a tool to automatically extract mentions of computational resources from papers. bioNerDS was used to analyze over 1.8 million mentions from 230,000 open access articles, finding patterns in resource usage over time and between journals. Challenges included ambiguity, variability in names, and extracting methods from ordered resource mentions. The goal is to provide a way to extract "best practices" for any resource-based domain by mining the literature.
RNASeq - Analysis Pipeline for Differential ExpressionJatinder Singh
RNA-Seq is a technique that uses next generation sequencing to sequence RNA transcripts and quantify gene expression levels. It can be used to estimate transcript abundance, detect alternative splicing, and compare gene expression profiles between healthy and diseased tissue. Computational challenges include read mapping due to exon-exon junctions and normalization of read counts. Key steps in RNA-Seq analysis include read mapping, transcript assembly, counting and normalizing reads, and detecting differentially expressed genes.
As increasing numbers of people choose to have their genomes sequenced and made available for research, more genomic data is available for analysis by machine learning approaches. Single Nucleotide Polymorphisms (SNPs) are known to be a major factor influencing many physical traits, diseases and other phenotypes. Using publicly available data and tools we predict phenotype from genotype using SNP data (1 to 2 million SNPs). We utilize data analysis and machine learning approaches only, no domain knowledge, so that our automated approach may be generally used to predict different phenotypes from genotype. In the first application of our method we predicted eye color with 87% accuracy.
RNA sequencing analysis tutorial with NGSHAMNAHAMNA8
This document provides an overview of RNA-seq data analysis. It discusses quality control of sequencing data using tools like FastQC, mapping reads to a reference genome or transcriptome using aligners like BWA and TopHat, and summarizing reads using counting tools to obtain read counts for each gene. These counts can then be used to estimate gene expression levels and perform differential expression analysis to identify genes with different expression between samples or conditions.
This document provides information about bioinformatics resources including databases of nucleotide and protein sequences. It discusses flat file databases like GenBank that store sequence data in plain text files and relational databases that improve data organization. Examples of popular biological databases are described, such as GenBank, EMBL, and DDBJ for nucleotide sequences and Swiss-Prot and TrEMBL for protein sequences. The document also covers sequence file formats, web tools for querying databases, and trace files used in sequence assembly.
Course: Bioinformatics for Biomedical Research (2014).
Session: 4.1- Introduction to RNA-seq and RNA-seq Data Analysis.
Statistics and Bioinformatisc Unit (UEB) & High Technology Unit (UAT) from Vall d'Hebron Research Institute (www.vhir.org), Barcelona.
This document provides an overview of RNA-seq and its applications. It discusses key aspects of RNA-seq including transcriptome profiling, alignment, quantification, differential expression analysis, clustering and visualization. It also covers experimental design considerations and highlights some commonly used tools and software. The document is a comprehensive guide that describes the RNA-seq workflow and analysis from start to finish.
University of Manchester Symposium 2012: Extraction and Representation of in ...geraintduck
This document describes research extracting and analyzing biological methods mentioned in the scientific literature. It developed bioNerDS, a tool to automatically extract mentions of computational resources from papers. bioNerDS was used to analyze over 1.8 million mentions from 230,000 open access articles, finding patterns in resource usage over time and between journals. Challenges included ambiguity, variability in names, and extracting methods from ordered resource mentions. The goal is to provide a way to extract "best practices" for any resource-based domain by mining the literature.
RNASeq - Analysis Pipeline for Differential ExpressionJatinder Singh
RNA-Seq is a technique that uses next generation sequencing to sequence RNA transcripts and quantify gene expression levels. It can be used to estimate transcript abundance, detect alternative splicing, and compare gene expression profiles between healthy and diseased tissue. Computational challenges include read mapping due to exon-exon junctions and normalization of read counts. Key steps in RNA-Seq analysis include read mapping, transcript assembly, counting and normalizing reads, and detecting differentially expressed genes.
As increasing numbers of people choose to have their genomes sequenced and made available for research, more genomic data is available for analysis by machine learning approaches. Single Nucleotide Polymorphisms (SNPs) are known to be a major factor influencing many physical traits, diseases and other phenotypes. Using publicly available data and tools we predict phenotype from genotype using SNP data (1 to 2 million SNPs). We utilize data analysis and machine learning approaches only, no domain knowledge, so that our automated approach may be generally used to predict different phenotypes from genotype. In the first application of our method we predicted eye color with 87% accuracy.
RNA sequencing analysis tutorial with NGSHAMNAHAMNA8
This document provides an overview of RNA-seq data analysis. It discusses quality control of sequencing data using tools like FastQC, mapping reads to a reference genome or transcriptome using aligners like BWA and TopHat, and summarizing reads using counting tools to obtain read counts for each gene. These counts can then be used to estimate gene expression levels and perform differential expression analysis to identify genes with different expression between samples or conditions.
Scaling Genetic Data Analysis with Apache Spark with Jon Bloom and Tim PoterbaDatabricks
In 2001, it cost ~$100M to sequence a single human genome. In 2014, due to dramatic improvements in sequencing technology far outpacing Moore’s law, we entered the era of the $1,000 genome. At the same time, the power of genetics to impact medicine has become evident. For example, drugs with supporting genetic evidence are twice as likely to succeed in clinical trials. These factors have led to an explosion in the volume of genetic data, in the face of which existing analysis tools are breaking down.
As a result, the Broad Institute began the open-source Hail project (https://hail.is), a scalable platform built on Apache Spark, to enable the worldwide genetics community to build, share and apply new tools. Hail is focused on variant-level (post-read) data; querying genetic data, as well as annotations, on variants and samples; and performing rare and common variant association analyses. Hail has already been used to analyze datasets with hundreds of thousands of exomes and tens of thousands of whole genomes, enabling dozens of major research projects.
This document summarizes benchmarking of germline small variant calling using Genome in a Bottle (GIAB) reference materials. It highlights best practices for benchmarking, including using benchmarking tools like hap.py and stratified performance metrics. It demonstrates benchmarking an Illumina HiSeq dataset aligned and called against GRCh37 using hap.py and stratifications from the GA4GH benchmarking tool. The results show precision and recall metrics with confidence intervals to evaluate performance across variant classes and difficulty levels. Ongoing work includes developing GIAB resources for GRCh38 and structural variants.
The document summarizes the work of the Genome in a Bottle Consortium to develop reference materials for benchmarking human structural variant calls. The Consortium has characterized structural variants over 50 base pairs in size across five human genomes using multiple long-read and linked-read sequencing technologies. The characterized variants are released as benchmark sets to evaluate the accuracy of different sequencing technologies in detecting structural variants. Ongoing work includes improving benchmarks for complex variants and collaborating to characterize more difficult genomic regions.
Neuroscience core lecture given at the Icahn school of medicine at Mount Sinai. This is the version 2 of the same topic. I have made some modifications to give a more gentle introduction and add a new example for ngs.plot.
GIAB Benchmarks for SVs and Repeats for stanford genetics sv 200511GenomeInABottle
This document provides an overview of the Genome in a Bottle (GIAB) Consortium's efforts to develop human genome reference materials and benchmarks for evaluating genome sequencing and variant calling. It summarizes the characterization of 7 human genomes, including developing variant calls, regions, and reference values. It also describes new efforts using linked and long reads to characterize structural variants and difficult genomic regions. The goal is to provide reference materials and benchmarks to help evaluate sequencing performance and accuracy across different technologies and algorithms.
This document summarizes the Genome in a Bottle (GIAB) Consortium's efforts to characterize structural variants in human genomes to serve as benchmarks. The GIAB Consortium has generated structural variant calls for 7 human genomes using diverse data types and analysis methods. The document describes the GIAB Consortium's process for integrating these data to identify high-confidence structural variant calls to include in version 0.6 of the structural variant benchmark set. It provides examples of different types of structural variants characterized and evaluates the trustworthiness of the benchmark calls based on independent validation. The document also discusses ongoing efforts to further improve structural variant characterization using emerging long-read technologies.
This document discusses the Matched Annotation from NCBI and EMBL-EBI (MANE) project. The project aims to define a set of identical reference transcripts between RefSeq and Ensembl/GENCODE for protein-coding genes. The MANE set will include a "Select" transcript that is representative of each gene locus, as well as additional "Plus" and "Extended" transcripts. The methodology involves choosing the most representative transcript based on expression, conservation, and manual curation. 5' and 3' ends will be matched based on CAGE and polyA sequencing data. The project aims to initially match 50% of genes and have the dataset available in late 2018, with the goal of matching 90%
This document outlines a 12-step program for biology to adapt to the era of data-intensive science. It summarizes the author's background and research interests. It then discusses the rapid growth of biological data from techniques like DNA sequencing. It introduces the concept of digital normalization as a way to efficiently process large transcriptome datasets. Finally, it outlines some proposed steps for the field, including investing in computational training, a focus on biological questions, and moving to continuous data updating models.
Fruit breedomics workshop wp6 from marker assisted breeding to genomics assis...fruitbreedomics
The document discusses strategies for genotyping using single nucleotide polymorphisms (SNPs). It describes different types of molecular markers that have been used over time, including restriction fragment length polymorphisms (RFLPs), random amplified polymorphic DNA (RAPDs), simple sequence repeats (SSRs), amplified fragment length polymorphisms (AFLPs) and SNPs. It also provides details on different SNP genotyping techniques ranging from low to high throughput, such as gel electrophoresis, fluorescent PCR, mass spectrometry and various array-based methods. The document outlines the process of developing a high density 480K SNP array for apple, including SNP discovery by resequencing accessions and filtering SNPs for the array design.
Enabling Biobank-Scale Genomic Processing with Spark SQLDatabricks
With the size of genomic data doubling every seven months, existing tools in the genomic space designed for the gigabyte scale tip over when used to process the terabytes of data being made available by current biobank-scale efforts. To enable common genomic analyses at massive scale while being flexible to ad-hoc analysis, Databricks and Regeneron Genetics Center have partnered to launch an open-source project.
The project includes optimized DataFrame readers for loading genomics data formats, as well as Spark SQL functions to perform statistical tests and quality control analyses on genomic data. We discuss a variety of real-world use cases for processing genomic variant data, which represents how an individual’s genomic sequence differs from the average human genome. Two use cases we will discuss are: joint genotyping, in which multiple individuals’ genomes are analyzed as a group to improve the accuracy of identifying true variants; and variant effect annotation, which annotates variants with their predicted biological impact. Enabling such workflows on Spark follows a straightforward model: we ingest flat files into DataFrames, prepare the data for processing with common Spark SQL primitives, perform the processing on each partition or row with existing genomic analysis tools, and save the results to Delta or flat files.
Genome engineering using CRISPR/Cas9 has several advantages over traditional gene targeting methods: it is faster, more precise, applicable to many species, and less expensive. CRISPR/Cas9 uses the Cas9 nuclease guided by a single guide RNA to introduce double-strand breaks at targeted genomic loci. This can generate gene knockouts through error-prone non-homologous end joining or allow for targeted insertions and modifications through homology-directed repair. While CRISPR/Cas9 has great potential, careful design of guide RNAs and donor templates is needed to minimize off-target effects.
This document provides information about different sequencing platforms and their characteristics. It compares Illumina, PacBio and Oxford Nanopore platforms in terms of average read length, advantages, limitations and recommended material. It also provides a comparison table of long-range sequencing platforms including their throughput per run, number of human genomes per run and cost per genome.
This document summarizes the process used to benchmark large deletion calls from multiple sequencing technologies and bioinformatics pipelines. Researchers merged deletion calls from 14 datasets into regions and evaluated call size accuracy. Calls supported by two or more technologies were identified as draft benchmark calls. Sensitivity to these calls was calculated for each method. The results provide insight into strengths and weaknesses of different approaches to structural variant detection.
This document provides an overview and introduction to RNA-seq analysis using Next Generation Sequencing. It discusses the RNA-seq workflow including mapping reads with TopHat2, transcript assembly with Cufflinks, and differential expression analysis. Key points covered include the advantages of RNA-seq over microarrays, the exponential drop in sequencing costs, mapping strategies for junction reads including TopHat, and running TopHat from the command line.
Learn from influencers. Influencers play a crucial role when it comes to marketing brands. ...
Use social media tools for research. ...
Use hashtag aggregators and analytics tools. ...
Know your hashtags. ...
Find a unique hashtag. ...
Use clear hashtags. ...
Keep It short and simple. ...
Make sure the hashtag is relevant.
The ionization state of a chemical, reflected in pKa values, affects lipophilicity, solubility, protein binding and the ability of a chemical to cross the plasma membrane. These properties govern the pharmacokinetic parameters such as absorption, distribution, metabolism, excretion and toxicity and thus pKa is a fundamental chemical property and is used in many models of chemical toxicity.
Experimentally determining pKa is not feasible for high-throughput assays. Predicting pKa is challenging and existing models have been developed only using restricted chemical space (e.g., anilines, phenols, benzoic acids, primary amines) and lack of a generalized model impedes ADME modeling.
No free and open source models exist for heterogeneous chemical classes, however, several proprietary programs exist. In this work, pKa open data bundled with DataWarrior (http://www.openmolecules.org/) were used to develop predictive models for pKa. After data cleaning, there were ~3100 and ~3900 monoprotic chemicals with an acidic or basic pKa, respectively. 1D and 2D chemical descriptors (AlogP, Topological polar surface area, etc) in addition to 12 fingerprints (presence or absence of a chemical group) were generated using PaDEL software. Three datasets were used: acidic, basic and acidic and basic combined.
13 datasets were examined, the 1D/2D descriptors and 12 fingerprints. Using the Extreme Gradient Boosting algorithm showed that the MACCS and Substructure Count fingerprints yielded the best results, with models showing an R-Squared of ~0.78 and a RMSE of 1.42.
Recently, Deep Learning models have showed remarkable progress in image recognition and natural language processing. To determine if the Deep Learning algorithms would increase model performance we examined the datasets and found that the Deep Learning models were somewhat superior than Extreme Gradient Boosting with an R-Squared of ~0.80 and an RMSE of ~1.38.
This work does not reflect U.S. EPA policy.
Genome in a Bottle - Towards new benchmarks for the “dark matter” of the huma...GenomeInABottle
The document discusses Genome in a Bottle (GIAB) and its efforts to characterize human genomes and provide reference materials and benchmarks to evaluate genome sequencing and variant calling. Specifically, it summarizes how GIAB has characterized 7 human genomes, provides extensive public sequencing data for benchmarking, and is now using linked and long reads to expand the small variant benchmark set, develop a structural variant benchmark, and perform diploid assembly of difficult regions. It also shows how new benchmarks that include more difficult regions have revealed errors in previous benchmarks and reduced performance metrics for variant calling tools.
Scaling Genetic Data Analysis with Apache Spark with Jon Bloom and Tim PoterbaDatabricks
In 2001, it cost ~$100M to sequence a single human genome. In 2014, due to dramatic improvements in sequencing technology far outpacing Moore’s law, we entered the era of the $1,000 genome. At the same time, the power of genetics to impact medicine has become evident. For example, drugs with supporting genetic evidence are twice as likely to succeed in clinical trials. These factors have led to an explosion in the volume of genetic data, in the face of which existing analysis tools are breaking down.
As a result, the Broad Institute began the open-source Hail project (https://hail.is), a scalable platform built on Apache Spark, to enable the worldwide genetics community to build, share and apply new tools. Hail is focused on variant-level (post-read) data; querying genetic data, as well as annotations, on variants and samples; and performing rare and common variant association analyses. Hail has already been used to analyze datasets with hundreds of thousands of exomes and tens of thousands of whole genomes, enabling dozens of major research projects.
This document summarizes benchmarking of germline small variant calling using Genome in a Bottle (GIAB) reference materials. It highlights best practices for benchmarking, including using benchmarking tools like hap.py and stratified performance metrics. It demonstrates benchmarking an Illumina HiSeq dataset aligned and called against GRCh37 using hap.py and stratifications from the GA4GH benchmarking tool. The results show precision and recall metrics with confidence intervals to evaluate performance across variant classes and difficulty levels. Ongoing work includes developing GIAB resources for GRCh38 and structural variants.
The document summarizes the work of the Genome in a Bottle Consortium to develop reference materials for benchmarking human structural variant calls. The Consortium has characterized structural variants over 50 base pairs in size across five human genomes using multiple long-read and linked-read sequencing technologies. The characterized variants are released as benchmark sets to evaluate the accuracy of different sequencing technologies in detecting structural variants. Ongoing work includes improving benchmarks for complex variants and collaborating to characterize more difficult genomic regions.
Neuroscience core lecture given at the Icahn school of medicine at Mount Sinai. This is the version 2 of the same topic. I have made some modifications to give a more gentle introduction and add a new example for ngs.plot.
GIAB Benchmarks for SVs and Repeats for stanford genetics sv 200511GenomeInABottle
This document provides an overview of the Genome in a Bottle (GIAB) Consortium's efforts to develop human genome reference materials and benchmarks for evaluating genome sequencing and variant calling. It summarizes the characterization of 7 human genomes, including developing variant calls, regions, and reference values. It also describes new efforts using linked and long reads to characterize structural variants and difficult genomic regions. The goal is to provide reference materials and benchmarks to help evaluate sequencing performance and accuracy across different technologies and algorithms.
This document summarizes the Genome in a Bottle (GIAB) Consortium's efforts to characterize structural variants in human genomes to serve as benchmarks. The GIAB Consortium has generated structural variant calls for 7 human genomes using diverse data types and analysis methods. The document describes the GIAB Consortium's process for integrating these data to identify high-confidence structural variant calls to include in version 0.6 of the structural variant benchmark set. It provides examples of different types of structural variants characterized and evaluates the trustworthiness of the benchmark calls based on independent validation. The document also discusses ongoing efforts to further improve structural variant characterization using emerging long-read technologies.
This document discusses the Matched Annotation from NCBI and EMBL-EBI (MANE) project. The project aims to define a set of identical reference transcripts between RefSeq and Ensembl/GENCODE for protein-coding genes. The MANE set will include a "Select" transcript that is representative of each gene locus, as well as additional "Plus" and "Extended" transcripts. The methodology involves choosing the most representative transcript based on expression, conservation, and manual curation. 5' and 3' ends will be matched based on CAGE and polyA sequencing data. The project aims to initially match 50% of genes and have the dataset available in late 2018, with the goal of matching 90%
This document outlines a 12-step program for biology to adapt to the era of data-intensive science. It summarizes the author's background and research interests. It then discusses the rapid growth of biological data from techniques like DNA sequencing. It introduces the concept of digital normalization as a way to efficiently process large transcriptome datasets. Finally, it outlines some proposed steps for the field, including investing in computational training, a focus on biological questions, and moving to continuous data updating models.
Fruit breedomics workshop wp6 from marker assisted breeding to genomics assis...fruitbreedomics
The document discusses strategies for genotyping using single nucleotide polymorphisms (SNPs). It describes different types of molecular markers that have been used over time, including restriction fragment length polymorphisms (RFLPs), random amplified polymorphic DNA (RAPDs), simple sequence repeats (SSRs), amplified fragment length polymorphisms (AFLPs) and SNPs. It also provides details on different SNP genotyping techniques ranging from low to high throughput, such as gel electrophoresis, fluorescent PCR, mass spectrometry and various array-based methods. The document outlines the process of developing a high density 480K SNP array for apple, including SNP discovery by resequencing accessions and filtering SNPs for the array design.
Enabling Biobank-Scale Genomic Processing with Spark SQLDatabricks
With the size of genomic data doubling every seven months, existing tools in the genomic space designed for the gigabyte scale tip over when used to process the terabytes of data being made available by current biobank-scale efforts. To enable common genomic analyses at massive scale while being flexible to ad-hoc analysis, Databricks and Regeneron Genetics Center have partnered to launch an open-source project.
The project includes optimized DataFrame readers for loading genomics data formats, as well as Spark SQL functions to perform statistical tests and quality control analyses on genomic data. We discuss a variety of real-world use cases for processing genomic variant data, which represents how an individual’s genomic sequence differs from the average human genome. Two use cases we will discuss are: joint genotyping, in which multiple individuals’ genomes are analyzed as a group to improve the accuracy of identifying true variants; and variant effect annotation, which annotates variants with their predicted biological impact. Enabling such workflows on Spark follows a straightforward model: we ingest flat files into DataFrames, prepare the data for processing with common Spark SQL primitives, perform the processing on each partition or row with existing genomic analysis tools, and save the results to Delta or flat files.
Genome engineering using CRISPR/Cas9 has several advantages over traditional gene targeting methods: it is faster, more precise, applicable to many species, and less expensive. CRISPR/Cas9 uses the Cas9 nuclease guided by a single guide RNA to introduce double-strand breaks at targeted genomic loci. This can generate gene knockouts through error-prone non-homologous end joining or allow for targeted insertions and modifications through homology-directed repair. While CRISPR/Cas9 has great potential, careful design of guide RNAs and donor templates is needed to minimize off-target effects.
This document provides information about different sequencing platforms and their characteristics. It compares Illumina, PacBio and Oxford Nanopore platforms in terms of average read length, advantages, limitations and recommended material. It also provides a comparison table of long-range sequencing platforms including their throughput per run, number of human genomes per run and cost per genome.
This document summarizes the process used to benchmark large deletion calls from multiple sequencing technologies and bioinformatics pipelines. Researchers merged deletion calls from 14 datasets into regions and evaluated call size accuracy. Calls supported by two or more technologies were identified as draft benchmark calls. Sensitivity to these calls was calculated for each method. The results provide insight into strengths and weaknesses of different approaches to structural variant detection.
This document provides an overview and introduction to RNA-seq analysis using Next Generation Sequencing. It discusses the RNA-seq workflow including mapping reads with TopHat2, transcript assembly with Cufflinks, and differential expression analysis. Key points covered include the advantages of RNA-seq over microarrays, the exponential drop in sequencing costs, mapping strategies for junction reads including TopHat, and running TopHat from the command line.
Learn from influencers. Influencers play a crucial role when it comes to marketing brands. ...
Use social media tools for research. ...
Use hashtag aggregators and analytics tools. ...
Know your hashtags. ...
Find a unique hashtag. ...
Use clear hashtags. ...
Keep It short and simple. ...
Make sure the hashtag is relevant.
The ionization state of a chemical, reflected in pKa values, affects lipophilicity, solubility, protein binding and the ability of a chemical to cross the plasma membrane. These properties govern the pharmacokinetic parameters such as absorption, distribution, metabolism, excretion and toxicity and thus pKa is a fundamental chemical property and is used in many models of chemical toxicity.
Experimentally determining pKa is not feasible for high-throughput assays. Predicting pKa is challenging and existing models have been developed only using restricted chemical space (e.g., anilines, phenols, benzoic acids, primary amines) and lack of a generalized model impedes ADME modeling.
No free and open source models exist for heterogeneous chemical classes, however, several proprietary programs exist. In this work, pKa open data bundled with DataWarrior (http://www.openmolecules.org/) were used to develop predictive models for pKa. After data cleaning, there were ~3100 and ~3900 monoprotic chemicals with an acidic or basic pKa, respectively. 1D and 2D chemical descriptors (AlogP, Topological polar surface area, etc) in addition to 12 fingerprints (presence or absence of a chemical group) were generated using PaDEL software. Three datasets were used: acidic, basic and acidic and basic combined.
13 datasets were examined, the 1D/2D descriptors and 12 fingerprints. Using the Extreme Gradient Boosting algorithm showed that the MACCS and Substructure Count fingerprints yielded the best results, with models showing an R-Squared of ~0.78 and a RMSE of 1.42.
Recently, Deep Learning models have showed remarkable progress in image recognition and natural language processing. To determine if the Deep Learning algorithms would increase model performance we examined the datasets and found that the Deep Learning models were somewhat superior than Extreme Gradient Boosting with an R-Squared of ~0.80 and an RMSE of ~1.38.
This work does not reflect U.S. EPA policy.
Genome in a Bottle - Towards new benchmarks for the “dark matter” of the huma...GenomeInABottle
The document discusses Genome in a Bottle (GIAB) and its efforts to characterize human genomes and provide reference materials and benchmarks to evaluate genome sequencing and variant calling. Specifically, it summarizes how GIAB has characterized 7 human genomes, provides extensive public sequencing data for benchmarking, and is now using linked and long reads to expand the small variant benchmark set, develop a structural variant benchmark, and perform diploid assembly of difficult regions. It also shows how new benchmarks that include more difficult regions have revealed errors in previous benchmarks and reduced performance metrics for variant calling tools.
Similar to SMBM 2012: Ambiguity and Variability of Database and Software Names in Bioinformatics (20)
Microbial interaction
Microorganisms interacts with each other and can be physically associated with another organisms in a variety of ways.
One organism can be located on the surface of another organism as an ectobiont or located within another organism as endobiont.
Microbial interaction may be positive such as mutualism, proto-cooperation, commensalism or may be negative such as parasitism, predation or competition
Types of microbial interaction
Positive interaction: mutualism, proto-cooperation, commensalism
Negative interaction: Ammensalism (antagonism), parasitism, predation, competition
I. Mutualism:
It is defined as the relationship in which each organism in interaction gets benefits from association. It is an obligatory relationship in which mutualist and host are metabolically dependent on each other.
Mutualistic relationship is very specific where one member of association cannot be replaced by another species.
Mutualism require close physical contact between interacting organisms.
Relationship of mutualism allows organisms to exist in habitat that could not occupied by either species alone.
Mutualistic relationship between organisms allows them to act as a single organism.
Examples of mutualism:
i. Lichens:
Lichens are excellent example of mutualism.
They are the association of specific fungi and certain genus of algae. In lichen, fungal partner is called mycobiont and algal partner is called
II. Syntrophism:
It is an association in which the growth of one organism either depends on or improved by the substrate provided by another organism.
In syntrophism both organism in association gets benefits.
Compound A
Utilized by population 1
Compound B
Utilized by population 2
Compound C
utilized by both Population 1+2
Products
In this theoretical example of syntrophism, population 1 is able to utilize and metabolize compound A, forming compound B but cannot metabolize beyond compound B without co-operation of population 2. Population 2is unable to utilize compound A but it can metabolize compound B forming compound C. Then both population 1 and 2 are able to carry out metabolic reaction which leads to formation of end product that neither population could produce alone.
Examples of syntrophism:
i. Methanogenic ecosystem in sludge digester
Methane produced by methanogenic bacteria depends upon interspecies hydrogen transfer by other fermentative bacteria.
Anaerobic fermentative bacteria generate CO2 and H2 utilizing carbohydrates which is then utilized by methanogenic bacteria (Methanobacter) to produce methane.
ii. Lactobacillus arobinosus and Enterococcus faecalis:
In the minimal media, Lactobacillus arobinosus and Enterococcus faecalis are able to grow together but not alone.
The synergistic relationship between E. faecalis and L. arobinosus occurs in which E. faecalis require folic acid
Evidence of Jet Activity from the Secondary Black Hole in the OJ 287 Binary S...Sérgio Sacani
Wereport the study of a huge optical intraday flare on 2021 November 12 at 2 a.m. UT in the blazar OJ287. In the binary black hole model, it is associated with an impact of the secondary black hole on the accretion disk of the primary. Our multifrequency observing campaign was set up to search for such a signature of the impact based on a prediction made 8 yr earlier. The first I-band results of the flare have already been reported by Kishore et al. (2024). Here we combine these data with our monitoring in the R-band. There is a big change in the R–I spectral index by 1.0 ±0.1 between the normal background and the flare, suggesting a new component of radiation. The polarization variation during the rise of the flare suggests the same. The limits on the source size place it most reasonably in the jet of the secondary BH. We then ask why we have not seen this phenomenon before. We show that OJ287 was never before observed with sufficient sensitivity on the night when the flare should have happened according to the binary model. We also study the probability that this flare is just an oversized example of intraday variability using the Krakow data set of intense monitoring between 2015 and 2023. We find that the occurrence of a flare of this size and rapidity is unlikely. In machine-readable Tables 1 and 2, we give the full orbit-linked historical light curve of OJ287 as well as the dense monitoring sample of Krakow.
SDSS1335+0728: The awakening of a ∼ 106M⊙ black hole⋆Sérgio Sacani
Context. The early-type galaxy SDSS J133519.91+072807.4 (hereafter SDSS1335+0728), which had exhibited no prior optical variations during the preceding two decades, began showing significant nuclear variability in the Zwicky Transient Facility (ZTF) alert stream from December 2019 (as ZTF19acnskyy). This variability behaviour, coupled with the host-galaxy properties, suggests that SDSS1335+0728 hosts a ∼ 106M⊙ black hole (BH) that is currently in the process of ‘turning on’. Aims. We present a multi-wavelength photometric analysis and spectroscopic follow-up performed with the aim of better understanding the origin of the nuclear variations detected in SDSS1335+0728. Methods. We used archival photometry (from WISE, 2MASS, SDSS, GALEX, eROSITA) and spectroscopic data (from SDSS and LAMOST) to study the state of SDSS1335+0728 prior to December 2019, and new observations from Swift, SOAR/Goodman, VLT/X-shooter, and Keck/LRIS taken after its turn-on to characterise its current state. We analysed the variability of SDSS1335+0728 in the X-ray/UV/optical/mid-infrared range, modelled its spectral energy distribution prior to and after December 2019, and studied the evolution of its UV/optical spectra. Results. From our multi-wavelength photometric analysis, we find that: (a) since 2021, the UV flux (from Swift/UVOT observations) is four times brighter than the flux reported by GALEX in 2004; (b) since June 2022, the mid-infrared flux has risen more than two times, and the W1−W2 WISE colour has become redder; and (c) since February 2024, the source has begun showing X-ray emission. From our spectroscopic follow-up, we see that (i) the narrow emission line ratios are now consistent with a more energetic ionising continuum; (ii) broad emission lines are not detected; and (iii) the [OIII] line increased its flux ∼ 3.6 years after the first ZTF alert, which implies a relatively compact narrow-line-emitting region. Conclusions. We conclude that the variations observed in SDSS1335+0728 could be either explained by a ∼ 106M⊙ AGN that is just turning on or by an exotic tidal disruption event (TDE). If the former is true, SDSS1335+0728 is one of the strongest cases of an AGNobserved in the process of activating. If the latter were found to be the case, it would correspond to the longest and faintest TDE ever observed (or another class of still unknown nuclear transient). Future observations of SDSS1335+0728 are crucial to further understand its behaviour. Key words. galaxies: active– accretion, accretion discs– galaxies: individual: SDSS J133519.91+072807.4
Discovery of An Apparent Red, High-Velocity Type Ia Supernova at 𝐳 = 2.9 wi...Sérgio Sacani
We present the JWST discovery of SN 2023adsy, a transient object located in a host galaxy JADES-GS
+
53.13485
−
27.82088
with a host spectroscopic redshift of
2.903
±
0.007
. The transient was identified in deep James Webb Space Telescope (JWST)/NIRCam imaging from the JWST Advanced Deep Extragalactic Survey (JADES) program. Photometric and spectroscopic followup with NIRCam and NIRSpec, respectively, confirm the redshift and yield UV-NIR light-curve, NIR color, and spectroscopic information all consistent with a Type Ia classification. Despite its classification as a likely SN Ia, SN 2023adsy is both fairly red (
�
(
�
−
�
)
∼
0.9
) despite a host galaxy with low-extinction and has a high Ca II velocity (
19
,
000
±
2
,
000
km/s) compared to the general population of SNe Ia. While these characteristics are consistent with some Ca-rich SNe Ia, particularly SN 2016hnk, SN 2023adsy is intrinsically brighter than the low-
�
Ca-rich population. Although such an object is too red for any low-
�
cosmological sample, we apply a fiducial standardization approach to SN 2023adsy and find that the SN 2023adsy luminosity distance measurement is in excellent agreement (
≲
1
�
) with
Λ
CDM. Therefore unlike low-
�
Ca-rich SNe Ia, SN 2023adsy is standardizable and gives no indication that SN Ia standardized luminosities change significantly with redshift. A larger sample of distant SNe Ia is required to determine if SN Ia population characteristics at high-
�
truly diverge from their low-
�
counterparts, and to confirm that standardized luminosities nevertheless remain constant with redshift.
Anti-Universe And Emergent Gravity and the Dark UniverseSérgio Sacani
Recent theoretical progress indicates that spacetime and gravity emerge together from the entanglement structure of an underlying microscopic theory. These ideas are best understood in Anti-de Sitter space, where they rely on the area law for entanglement entropy. The extension to de Sitter space requires taking into account the entropy and temperature associated with the cosmological horizon. Using insights from string theory, black hole physics and quantum information theory we argue that the positive dark energy leads to a thermal volume law contribution to the entropy that overtakes the area law precisely at the cosmological horizon. Due to the competition between area and volume law entanglement the microscopic de Sitter states do not thermalise at sub-Hubble scales: they exhibit memory effects in the form of an entropy displacement caused by matter. The emergent laws of gravity contain an additional ‘dark’ gravitational force describing the ‘elastic’ response due to the entropy displacement. We derive an estimate of the strength of this extra force in terms of the baryonic mass, Newton’s constant and the Hubble acceleration scale a0 = cH0, and provide evidence for the fact that this additional ‘dark gravity force’ explains the observed phenomena in galaxies and clusters currently attributed to dark matter.
This presentation offers a general idea of the structure of seed, seed production, management of seeds and its allied technologies. It also offers the concept of gene erosion and the practices used to control it. Nursery and gardening have been widely explored along with their importance in the related domain.
Holsinger, Bruce W. - Music, body and desire in medieval culture [2001].pdf
SMBM 2012: Ambiguity and Variability of Database and Software Names in Bioinformatics
1. Ambiguity
and
Variability
of
Database
and
So6ware
Names
in
Bioinforma:cs
SMBM
2012
Geraint
Duck1,
Robert
Stevens1,
David
Robertson2
and
Goran
Nenadic1
1School
of
Computer
Science,
2Faculty
of
Life
Sciences
The
University
of
Manchester
Manchester,
UK
2. Named
En:ty
Recogni:on
(NER)
• Variety
of
NER
uses
– Species
– Gene/protein
names
– Chemical
names
• Variety
of
NER
accuracy
– 95%
F-‐score
species
(LINNAEUS)
– 73%
F-‐score
(strict)
gene
name
(ABNER)
– Over
70%
F-‐score
chemical
names
(OSCAR3)
• Draw
parallels
for
database
and
so/ware
NER
2
4. Challenges
-‐
Ambiguity
• leg
• white
• cab
• C.
elegans
– 41
NCBI
taxonomy
species
• HIV
– Human
immunodeficiency
virus
– Human
immunovirus
• analysis
• Network
• graph
• DIP
– distal
interphalangeal
– Database
of
Interac:ng
Proteins
4
5. Challenges
-‐
Variability
• NF-‐kappaB
• NF-‐kappa
B
• NF-‐kappa-‐B
• NF-‐κB
• Case
variants
• Spelling
variants
• ClustalW
• Clustal
W
• Clustal-‐W
• CLUSTAL
W
• ClustalX
(GUI)?
• Now:
Clustal
Omega
5
6. Preliminary
• Annota:on
guidelines
– Database,
so6ware,
package,
ontology
names
– Not
file
formats,
algorithms,
tasks,
methods,
database
iden:fiers,
programming
languages,
opera:ng
systems,
etc.
• Gold
standard
corpus
– 25
from
BMC
Bioinforma:cs
and
PLoS
Computa:onal
Biology;
5
from
Genome
Biology
• Dic:onary
of
resource
names
– 4,879
unique
entries
from
10
online
resources
6
7. Preliminary
• Inter-‐annotator
agreement
– F-‐score:
86%
• 30
documents
– 1319
total
men:ons
– 224
unique
men:ons
Databases
So/ware
Combined
Precision
0.79
(0.66)
0.99
(0.96)
0.93
(0.87)
Recall
0.67
(0.56)
0.84
(0.82)
0.80
(0.74)
F-‐measure
0.73
(0.61)
0.91
(0.88)
0.86
(0.80)
Total
Number
of
Documents
30
Total
Database
and
So9ware
Men<ons
1319
Total
Unique
Resource
Men<ons
224
Percentage
of
Database
Men:ons
36%
Percentage
of
Unique
DB
Men:ons
26%
Average
Men:ons
per
Document
44
Average
Unique
Men:ons
per
Document
8.2
Max
Men:ons
in
a
Single
Document
227
Max
Unique
Men:ons
in
a
Document
33
Resources
with
only
a
Single
Men:on
117
7
8. Ambiguity
and
Variability
• Compared
names
to
– Acronym
Dic:onary:
1,933
– English
Dic:onary:
86,308
• Ambiguity
in
corpus:
– ≈
2%
(case-‐sensi:ve)
– ≈
12%
(case-‐insensi:ve)
• Ambiguity
in
names
dic:onary:
– ≈
0.1%
(case-‐sensi:ve)
– ≈
0.5%
(case-‐insensi:ve)
• 224
unique
names
– 45
were
variants
• 15
acronyms
• Orthographics
• Spellings
– 179
different
resources
• 79%
one
variant
• 17%
two
variants
• 4%
three
variants
8
9. Name
Composi:on
• Majority
are
single
nouns
– includes
acronyms
• 6%
lowercase
common
nouns
– affy,
bioconductor
• A
few
contained
numbers
– S4,
t2prhd
• A
few
misclassified
as
verbs
– …each
query
protein
is
first
BLASTed
with…
– …held
near
their
equilibrium
values
using
SHAKE.
– …graphical
representaPons
were
achieved
using
dot
v1.10…
NNP
68.0%
NNP
NNP
8.8%
NN
5.7%
NNP
NNP
NNP
5.3%
NNP
CD
3.1%
NNP
CD
.
CD
1.8%
NNP
NNP
NNP
NNP
NNP
1.3%
NNP
LS
0.9%
NNP
NNP
NNP
NNP
0.9%
Other
Pajerns
4.4%
9
10. Name
Composi:on
• Longest
Names
(most
tokens)
– Corpus:
5
–
Gene
Expression
Profile
Analysis
Suite
– Dic:onary:
12
–
PredicPon
of
Protein
SorPng
Signals
and
LocalisaPon
Sites
in
Amino
Acid
Sequences
• Evaluated
(stemmed)
token
frequencies
within
the
dic:onary
– Long-‐tail
curve
– 87%
used
only
once
– High
frequency
words
suggest
common
heads
and
bioinforma:cs
related
terms
10
12. Dic:onary
Matching
• F-‐score
under
55%
– Low
precision
• GO
(GO:0007089)
• cycle
• genomes
– Low
recall,
Incomprehensive
• i
Linker
• xPedPhase
• 95%
of
menPons
could
be
matched…
Dic:onary
matches
55.3%
Heads
and
Hearst
pajerns
9.7%
Title
appearances
0.6%
References
and
URLs
1.9%
Version
informa:on
1.2%
Noun/Verb
associa:ons
20.3%
Comparisons
5.8%
Remaining
5.2%
12
TP
FP
FN
P
R
F
Lenient
729
633
590
54%
55%
54%
Strict
695
667
624
51%
53%
52%
13. Poten:al
Clues
• Heads
– the
stochas:c
simulator
Dizzy
allows
...
– The
MethMarker
so9ware
was
...
– ...
system,
PSPE,
specifically
to
...
– tools:
CLUSTALW,
...,
and
MUSCLE.
– ...
programs
such
as
Simlink,
...,
and
SimPed.
• Titles
– CoXpress:
differen:al
co-‐
expression
in
gene
expression
data
– TABASCO:
A
single
molecule,
base-‐pair
resolved
gene
expression
simulator
– SimHap
GUI:
An
intui:ve
graphical
user
interface
for
gene:c
associa:on
analysis
13
14. Poten:al
Clues
• References
– Galaxy
[18]
and
EpiGRAPH
[19]
– The
learning
metrics
principle
[14,15]
• Versions
– using
dot
v1.10
and
Graphviz
1.13(v16).
– CLUSTAL
W
version
1.83
– Dynalign
4.5,
and
LocARNA
0.99
• Comparisons
– xPedPhase
did
beRer
than
i
Linker
– Cofogla2
with
this
cutoff
PSVM
gives
a
bejer
false
posi:ve
rate
compared
to
RNAz
– Foldalign
was
much
slower
than
Cofolga2
except
for
– Like
Moleculizer,
Tabasco
dynamically
generates
14
FP
15. Poten:al
Clues
• the
SimHap
GUI
installa<on.
• implemented
within
PedPhase
• Our
mo:va:ons
for
crea<ng
Tabasco
• MethMarker
therefore
provides
• A
typical
screenshot
of
MethMarker
• MethMarker’s
user
interface
reflects
• Tested
effect
on
precision
• Ran
regular
expression
• Percentage
of
sentences
with
resource
name
and
that
matched
regex:
– ran|run(ning|s)?
• 48%
– RAM
• 50%
– Website
• 77%
• …
so
are
plausible
clues.
15
16. Scope
• Database
• So6ware
• Method
• Approach
• Algorithm
• Task
• Programming
Language
• Records/Iden:fiers
• File
Formats
• Author’s
mix
vocab
• Fuzzy
dis:nc:on
• R
language,
R
so6ware
– Dis:nc:on?
• Microso6
Excel
– Lots
of
sta:s:cs
• Students
t-‐test
– Lots
of
sta:s:cs
tools
16
17. Summary
• Annota:on
guidelines
• Annotated
gold
corpus
• Evaluated
resource
name
men:ons
– Composi:on
– Ambiguity
– Variability
• Dic:onary
match:
<
55%
• Provide
poten:al
clues
for
capture
• Acknowledgments
– BBSRC
– Dan
Jamieson
–
IAA
• hjp://sourceforge.net/
projects/bionerds/
• Thank-‐you!
• Ques:ons?
17