Systems biology is the computational and mathematical modeling of complex biological systems. It is a biology-based interdisciplinary field of study that focuses on complex interactions within biological systems, using a holistic approach (holism instead of the more traditional reductionism) to biological research.
Genomic sequencing a sub-disciplinary branch of genetics and difference between the two sequencers used to sequence the genome basically automated sequencer and fluorescence sequencers and its applications.
SNP (Single Nucleotide Polymorphic), SNP mapping, SNP profile, SNP types, SNP analysis by gel electropherosis and by mass spectrometry, SNP effects, single strand conformation polymorphism, SNP advantages and disadvantages and application of SNP profile in drug choice
Introduction
Transcriptome analysis
Goal of functional genomics
Why we need functional genomics
Technique
1. At DNA level
2.At RNA level
3. At protein level
4. loss of function
5. functional genomic and bioinformatics
Application
Latest research and reviews
Websites of functional genomics
Conclusions
Reference
Uses of Artificial Intelligence in BioinformaticsPragya Pai
This presentation is about the usage of Artificial Intelligence in Bioinformatics. These slides give the basic knowledge about usage of Artificial Intelligence in Bioinformatics.
Systems biology is the computational and mathematical modeling of complex biological systems. It is a biology-based interdisciplinary field of study that focuses on complex interactions within biological systems, using a holistic approach (holism instead of the more traditional reductionism) to biological research.
Genomic sequencing a sub-disciplinary branch of genetics and difference between the two sequencers used to sequence the genome basically automated sequencer and fluorescence sequencers and its applications.
SNP (Single Nucleotide Polymorphic), SNP mapping, SNP profile, SNP types, SNP analysis by gel electropherosis and by mass spectrometry, SNP effects, single strand conformation polymorphism, SNP advantages and disadvantages and application of SNP profile in drug choice
Introduction
Transcriptome analysis
Goal of functional genomics
Why we need functional genomics
Technique
1. At DNA level
2.At RNA level
3. At protein level
4. loss of function
5. functional genomic and bioinformatics
Application
Latest research and reviews
Websites of functional genomics
Conclusions
Reference
Uses of Artificial Intelligence in BioinformaticsPragya Pai
This presentation is about the usage of Artificial Intelligence in Bioinformatics. These slides give the basic knowledge about usage of Artificial Intelligence in Bioinformatics.
Bioinformatics in biotechnology by kk sahu KAUSHAL SAHU
Introduction
Bioinformatics – definition
History
Required skills
Core areas of bioinformatics
Components of bioinformatics
Nomenclature system in bioinformatics
Biological databases
Types of database
Bioinformatics tools
Applications of bioinformatics
Conclusion
References
As an interdisciplinary field of science, bioinformatics combines biology, computer science, information engineering, mathematics and statistics to analyze and interpret the biological data.
bioinformatics algorithms and its basicssofav88068
Introduction to bioinformatics, this is where u will learn about basic bioinformatics and its applications . what is bioinformatics and why bioinformatics. the basic fata sequences and blast algorithms. the examples of human genome , DNA , the genetic material and the blueprint of the whole existence. the concept of bioinformatics which is a relatively new field and the tools used there and the pipelines are also new . bioinformatics the lord the Saviour the Christ idk what else to write to up the discoverability score this is completely senseless and useless.SlideShare is a platform where you can upload, present, and discover presentations and infographics from various topics and industries. Please click the link in that email to verify your identity. To learn more, please visit our a and the long live the king of the pirates Luffy will find the one piece this website is totally crap pirate things that is best I've write 1000 words and it still isn't enough idk what else to add this .
BIOLOGICAL DATABASES :
A biological database is a large, organized body of persistent data, usually associated with computerized software designed to update, query, and retrieve components of the data stored within the system.
The chief objective of the development of a database is to organize data in a set of structured records to enable easy retrieval of information.
Example. A few popular databases are GenBank from NCBI (National Center for Biotechnology Information), SwissProt from the Swiss Institute of Bioinformatics and PIR from the Protein Information Resource.
IMPORTANCE OF DATABASES :
1. Databases act as a store house of information.
2. Databases are used to store and organize data in such a way that information can be retrieved easily via a variety of search criteria.
3. It allows knowledge discovery, which refers to the identification of connections between pieces of information that were not known when the information was first entered. This facilitates the discovery of new biological insights from raw data.
4. Secondary databases have become the molecular biologist’s reference library over the past decade or so, providing a wealth of information on just about any gene or gene product that has been investigated by the research community.
5. It helps to solve cases where many users want to access the same entries of data.
6. Allows the indexing of data.
7. It helps to remove redundancy of data.
TYPES OF BIOLOGICAL DATABASES:
Biological databases are classified on
1. Based on content of biological data
2. Based on the nature of data.
1. BASED ON CONTENT OF BIOLOGICAL DATA :
Based on their contents, biological databases can be roughly divided into two categories:
1. Primary databases
2. Secondary databases
Bioinformatics Introduction and Use of BLAST ToolJesminBinti
Hi, I am Jesmin, studying MCSE. I think this file will help you if you want to know the basic information about Bioinformatics and the use of BLAST tool. The BLAST tool is the tool that matches the sequences of DNA,RNA and proteins.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Toxic effects of heavy metals : Lead and Arsenicsanjana502982
Heavy metals are naturally occuring metallic chemical elements that have relatively high density, and are toxic at even low concentrations. All toxic metals are termed as heavy metals irrespective of their atomic mass and density, eg. arsenic, lead, mercury, cadmium, thallium, chromium, etc.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Earliest Galaxies in the JADES Origins Field: Luminosity Function and Cosmic ...Sérgio Sacani
We characterize the earliest galaxy population in the JADES Origins Field (JOF), the deepest
imaging field observed with JWST. We make use of the ancillary Hubble optical images (5 filters
spanning 0.4−0.9µm) and novel JWST images with 14 filters spanning 0.8−5µm, including 7 mediumband filters, and reaching total exposure times of up to 46 hours per filter. We combine all our data
at > 2.3µm to construct an ultradeep image, reaching as deep as ≈ 31.4 AB mag in the stack and
30.3-31.0 AB mag (5σ, r = 0.1” circular aperture) in individual filters. We measure photometric
redshifts and use robust selection criteria to identify a sample of eight galaxy candidates at redshifts
z = 11.5 − 15. These objects show compact half-light radii of R1/2 ∼ 50 − 200pc, stellar masses of
M⋆ ∼ 107−108M⊙, and star-formation rates of SFR ∼ 0.1−1 M⊙ yr−1
. Our search finds no candidates
at 15 < z < 20, placing upper limits at these redshifts. We develop a forward modeling approach to
infer the properties of the evolving luminosity function without binning in redshift or luminosity that
marginalizes over the photometric redshift uncertainty of our candidate galaxies and incorporates the
impact of non-detections. We find a z = 12 luminosity function in good agreement with prior results,
and that the luminosity function normalization and UV luminosity density decline by a factor of ∼ 2.5
from z = 12 to z = 14. We discuss the possible implications of our results in the context of theoretical
models for evolution of the dark matter halo mass function.
DERIVATION OF MODIFIED BERNOULLI EQUATION WITH VISCOUS EFFECTS AND TERMINAL V...Wasswaderrick3
In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
3. An emerging discipline of Biotechnology which has now
become the heart of modern biological research.
Bioinformatics, was coined by Paulien Hogeweg, by
combining– Biology and Information Technology (IT).
Bioinformatics is the systematic development and application of
IT solutions to handle biological information by addressing
biological data collection and warehousing, data mining, database
searches, analyzes and interpretation, modeling and product
design.
4. The field of science in which biology, computer science
and information technology merge into a single discipline .
8. Computational Bioinformatics
It refers to all the computational work done so as to develop
an application that is aimed to address certain problems in biology.
Computational Bioinformatics further has the following levels:
Algorithm and Software Development:
To solve any problem we first must have a strategy
to tackle the problem For this algorithm of the
application is a must. Here people with different
expertise work together to develop an algorithm.
9. A molecular biologist put forward the problems
A bioinformaticist suggests the possible way of
handling the problem
A computer scientist or a system engineer designs
a framework
Software engineer and Mathematician/Statistician
design algorithm
Molecular biologist sits in the user end to evaluate
if the software fulfills his demands
How to develop an algorithm
10. Any information generated in the lab must be stored
in a database for easy retrieval in the future.
Without database bioinformatics becomes lame.
Database is a place where one can store related
information which makes the information much more
meaningful and help in the future development.
Database Construction and Curation:
11. APPLICATION BIOINFORMATICS:
This part of bioinformatics is directly related to users
including students as well as researchers. From this part output of
bioinformatics is obtained. Various bioinformatics application can
be categorized under following groups:
Sequence analysis
Functional analysis
Structural analysis
12. Sequence Analysis:
All the applications that analyzes various types of
sequence information and can compare between similar
types of information is grouped under Sequence
Analysis.
Function Analysis:
It mainly deals with functions of genes and their
products i.e. proteins.
Analysis Structure:
Structural Bioinformatics which is devoted to predict the
structure and possible roles of these structures of Proteins or
RNA.
13. AIMS OF BIOINFORMATICS
In general, there are three basic aims of bioinformatics…
The first aim of bioinformatics is to store the
biological data organized in form of a database. This
allows the researchers an easy access to existing
information and submit new entries.
14. The second aim is to develop tools and resources that aid
in the analysis of data. For example: BLAST to find out
similar nucleotide/amino-acid sequences, ClustalW to
align two or more nucleotide/amino-acid sequences.
The third and the most important aim of
bioinformatics is to exploit these computational tools to
analyze the biological data interpret the results in a
biologically meaningful manner.
15. RSEARCH AREAS OF BIOINFORMATICS
.
In experimental molecular biology
In Genetics and genomics, it aids in sequencing and
annotating genomes and their observed mutations
Textual mining of biological literature
Analysis of gene and protein expression and regulation
Understanding of evolutionary aspects of molecular
biology
Analyze and catalogue the biological pathways and
networks that are an important part of systems biology.
16.
17. BIOLOGICAL DATABASE
Biological databases are libraries of life sciences information,
collected from scientific experiments, published literature, high-
throughput experiment technology, and computational analyses.
They contain information from research areas including genomics,
proteomics, metabolomics, microarray gene expression, and
phylogenetics.
24. Types of Biological Databases According To
Their Function
Primary nucleotide sequence databases
The International Nucleotide Sequence Database (INSD)
consists of the following databases.
DNA Data Bank of Japan (National Institute of Genetics)
European Nucleotide Archive (European Bioinformatics
Institute)
GenBank (National Center for Biotechnology Information)
The three databases, are repositories for nucleotide sequence
data from all organisms.
25. Genome databases
These databases collect organism genome sequences,
annotate and analyze them, and provide public access.. These
databases may hold many species genomes, or a single model
organism genome.
Bioinformatic Harvester
SNPedia
CAMERA Resource for microbial genomics and metagenomics
Corn, the Maize Genetics and Genomics Database
EcoCyc a database that describes the genome and the biochemical
machinery of the model organism E. coli K-12
26. Protein sequence databases
UniProt: Universal Protein Resource (EBI, Swiss Institute of
Bioinformatics, PIR)
Swiss-Prot: Protein Knowledgebase (Swiss Institute of
Bioinformatics)
PROSITE: Database of Protein Families and Domains
Database of Interacting Proteins (Univ. of California)
Pfam: Protein families database of alignments and HMMs
(Sanger Institute)
27. Proteomics databases
Proteomics Identifications Database (PRIDE) A public
repository for proteomics data.. (European Bioinformatics Institute)
MitoMiner - A mitochondrial proteomics database (MRC
Mitochondrial Biology Unit)
GelMap - A public database of proteins identified on 2D gels
(University of Hanover Proteomics Department)
28. Protein structure databases
Protein Data Bank (PDB) comprising:
Protein DataBank in Europe (PDBe)
ProteinDatabank in Japan (PDBj)
(RCSB) Research Collaboratory for Structural
Bioinformatics
29. RNA databases
Rfam, a database of RNA families
miRBase , the microRNA database
snoRNAdb, a database of snoRNAs
31. How to Perform Database-Searching
As the amount of biological relevant data is
increasing so rapidly, it is essential to know how to
access and search information on them. There are
three data retrieval systems to molecular biologist:
Sequence Retrieval System (SRS), Entrez, and
DBGET.
32. SRS is a homogeneous interface to over 80
biological databases that had been developed at the
European Bioinformatics Institute (EBI) at Hinxton, UK.
It includes databases of sequences, metabolic
pathways, transcription factors, application results (like
BLAST, SSEARCH, FASTA), protein 3-D structures,
genomes, mappings, mutations, and locus specific
mutations.
Sequence Retrieval System (SRS)
33.
34. Database Description
PubMed The biomedical literature
Nucleotide Sequence database (genbank0
Protein Sequence database
Structure 3 D macromolecular structures
Genome Complete genome assemblies
PopSet Population study
OMIM On line Mendelian inheritance in man
Taxonomy Organisms in genbank
SNP Single nucleotide polymorphism
Conserved domains CDD
35. DBGET
DBGET is an integrated database retrieval
system, developed at the university of Tokyo.
Provided access to 20 databases, one at a time.
Having more limited options, the DBGET is less
recommended than the two others.