After sequencing of the genome has been done, the first thing that comes to mind is "Where are the genes?". Genome annotation is the process of attaching information to the biological sequences. It is an active area of research and it would help scientists a lot to undergo with their wet lab projects once they know the coding parts of a genome.
The document discusses Prosite, a database of protein family signatures that can be used to determine the function of uncharacterized proteins. It contains patterns and profiles formulated to identify which known protein family a new sequence belongs to. The Prosite database consists of two files - a data file containing information for scanning sequences, and a documentation file describing each pattern and profile. New Prosite entries are mainly profiles developed by collaborators at the SIB Swiss Institute of Bioinformatics to identify distantly related proteins based on conserved residues.
Comparative genomics in eukaryotes, organellesKAUSHAL SAHU
Comparative genomics involves comparing the genomic features of different organisms, such as DNA sequences, genes, and gene order. This field has revealed both similarities and differences between organisms that can provide insights into evolutionary relationships. Some of the first comparative genomic studies compared large DNA viruses. Since then, many complete genome sequences have been determined, including for yeast, fruit flies, worms, plants, mice, and humans. While humans have around 35,000 genes, complexity is not solely due to gene number. Comparative analysis of human and mouse genomes shows 40% sequence similarity and similar gene numbers, but different genome sizes. Mitochondrial genomes also yield insights when compared between domains of life. Computational tools like BLAST are used to facilitate genomic
The document discusses experimental and computational methods for protein structure prediction. Experimental methods like NMR, X-ray crystallography, and cryo-EM can accurately determine protein structure but require isolating and crystallizing the protein. Computational methods like homology modeling, ab initio modeling, and threading/folding predict structure from sequence alone and are less accurate but do not require crystallization. Computational methods work best when a template structure is available from experimental data. While experimental methods are very accurate, they are also costly and difficult for large numbers of proteins, making computational methods a useful complement despite being less accurate.
The Molecular Modeling Database (MMDB) is a database hosted by the National Center for Biotechnology Information that contains over 28,000 experimentally determined 3D structures of biomolecules including proteins and nucleic acids derived from the Protein Data Bank, excluding theoretical models. It facilitates computation and links structures to other data types. Each record cross-references its source PDB file. The database contains molecular structures, biological activity data, experimental data, chemical properties, and annotations to aid researchers. Examples of widely used molecular modeling databases discussed are the Protein Data Bank, PubChem, and RCSB Ligand Explorer.
This document discusses various bioinformatics tools and methods for identifying genes from genomic sequences. It begins by defining genes and genomes, then describes reference databases like RefSeq that are important for gene identification. It outlines the general workflow for gene identification, including obtaining sequences, preprocessing, annotation, prediction, and validation. Specific tools mentioned include GENSCAN, Glimmer, and Augustus for gene prediction, and BLAST for sequence alignment. The document also discusses identifying other genomic features like promoters, repeats, and open reading frames. It emphasizes that accurate gene identification requires both computational and experimental approaches.
Gene prediction is the process of determining where a coding gene might be in a genomic sequence. Functional proteins must begin with a Start codon (where DNA transcription begins), and end with a Stop codon (where transcription ends).
After sequencing of the genome has been done, the first thing that comes to mind is "Where are the genes?". Genome annotation is the process of attaching information to the biological sequences. It is an active area of research and it would help scientists a lot to undergo with their wet lab projects once they know the coding parts of a genome.
The document discusses Prosite, a database of protein family signatures that can be used to determine the function of uncharacterized proteins. It contains patterns and profiles formulated to identify which known protein family a new sequence belongs to. The Prosite database consists of two files - a data file containing information for scanning sequences, and a documentation file describing each pattern and profile. New Prosite entries are mainly profiles developed by collaborators at the SIB Swiss Institute of Bioinformatics to identify distantly related proteins based on conserved residues.
Comparative genomics in eukaryotes, organellesKAUSHAL SAHU
Comparative genomics involves comparing the genomic features of different organisms, such as DNA sequences, genes, and gene order. This field has revealed both similarities and differences between organisms that can provide insights into evolutionary relationships. Some of the first comparative genomic studies compared large DNA viruses. Since then, many complete genome sequences have been determined, including for yeast, fruit flies, worms, plants, mice, and humans. While humans have around 35,000 genes, complexity is not solely due to gene number. Comparative analysis of human and mouse genomes shows 40% sequence similarity and similar gene numbers, but different genome sizes. Mitochondrial genomes also yield insights when compared between domains of life. Computational tools like BLAST are used to facilitate genomic
The document discusses experimental and computational methods for protein structure prediction. Experimental methods like NMR, X-ray crystallography, and cryo-EM can accurately determine protein structure but require isolating and crystallizing the protein. Computational methods like homology modeling, ab initio modeling, and threading/folding predict structure from sequence alone and are less accurate but do not require crystallization. Computational methods work best when a template structure is available from experimental data. While experimental methods are very accurate, they are also costly and difficult for large numbers of proteins, making computational methods a useful complement despite being less accurate.
The Molecular Modeling Database (MMDB) is a database hosted by the National Center for Biotechnology Information that contains over 28,000 experimentally determined 3D structures of biomolecules including proteins and nucleic acids derived from the Protein Data Bank, excluding theoretical models. It facilitates computation and links structures to other data types. Each record cross-references its source PDB file. The database contains molecular structures, biological activity data, experimental data, chemical properties, and annotations to aid researchers. Examples of widely used molecular modeling databases discussed are the Protein Data Bank, PubChem, and RCSB Ligand Explorer.
This document discusses various bioinformatics tools and methods for identifying genes from genomic sequences. It begins by defining genes and genomes, then describes reference databases like RefSeq that are important for gene identification. It outlines the general workflow for gene identification, including obtaining sequences, preprocessing, annotation, prediction, and validation. Specific tools mentioned include GENSCAN, Glimmer, and Augustus for gene prediction, and BLAST for sequence alignment. The document also discusses identifying other genomic features like promoters, repeats, and open reading frames. It emphasizes that accurate gene identification requires both computational and experimental approaches.
Gene prediction is the process of determining where a coding gene might be in a genomic sequence. Functional proteins must begin with a Start codon (where DNA transcription begins), and end with a Stop codon (where transcription ends).
Genomics refers to the study of the entire genome of an organism. It deals with mapping genes on chromosomes and sequencing entire genomes. While work on genomics began with prokaryotes like bacteria, research has now been conducted on crop plants like rice and Arabidopsis thaliana. Genomics is an interdisciplinary field that uses tools from molecular biology, robotics, and computing to study genomes. It provides information on genome size, gene number, gene function, and evolution. Genomics has applications in crop improvement through gene mapping, marker-assisted selection, and transgenic breeding. However, genomic research also faces limitations due to high costs, technical challenges, and complexity of traits.
Introduction
Definition
History
Principle
Components of bioinformatics
Bioinformatics databases
Tools of bioinformatics
Applications of bioinformatics
Molecular medicine
Microbial genomics
Plant genomics
Animal genomics
Human genomics
Drug and vaccine designing
Proteomics
For studying biomolecular structures
In- silico testing
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.
The European Molecular Biology Laboratory (EMBL) is a molecular biology research institution supported by 22 member states. EMBL was created in 1974 and operates from five sites, performing basic research in molecular biology and molecular medicine. A key function of EMBL is the EMBL Nucleotide Sequence Database, maintained at the European Bioinformatics Institute, which incorporates and distributes nucleotide sequences from public sources as part of an international collaboration.
This document summarizes key aspects of sequence alignment. It discusses how sequence alignment involves comparing sequences to find identical or similar characters in the same order. It describes global and local alignment and the algorithms used for each. It also discusses scoring systems for alignments, including penalties for gaps and mismatches. The goals of sequence alignment are to infer functional, structural or evolutionary relationships between sequences.
The study of nucleic acids began with the discovery of DNA, progressed to the study of genes and small fragments, and has now exploded to the field of genomics. Genomics is the study of entire genomes, including the complete set of genes, their nucleotide sequence and organization, and their interactions within a species and with other species. The advances in genomics have been made possible by DNA sequencing technology. [Source: https://opentextbc.ca/biology/chapter/10-3-genomics-and-proteomics/]
description of functional genomics and structural genomics and the techniques involved in it and also decribing the models of forward genetics and techniques involved in it and reverse genetics and techniques involved in it
The document summarizes a bioinformatics summer camp, including:
1. The camp will cover basic molecular biology and bioinformatics topics like DNA, proteins, gene expression and the genetic code.
2. Students will work on computational analysis projects involving whole genome sequencing, gene expression profiling, and functional and comparative genomics.
3. The camp will teach techniques for analyzing protein structures and interactions, gene expression data, and identifying pockets on protein surfaces.
Composite: It compile and filter sequence data from primary database.
Specialized : database—allows targeted searching on one or more specific subject areas
This document discusses genome database systems. It begins with an introduction to bioinformatics and genomes. It then discusses the background of genome databases, including some examples. The major characteristics of genome database systems are described as having high complex data, schema changes at a rapid pace, and complex queries. The key areas of data management in genome databases are discussed as non-standard data, complex queries, data interpretation, integration across databases, and uniform management solutions. Major research areas and applications that impact society are also summarized.
This document provides an overview of DNA sequencing technologies. It begins with a brief history of DNA sequencing, including the discovery of DNA's structure and Sanger sequencing. The document then focuses on next generation sequencing technologies, describing several platforms such as 454 sequencing, Illumina sequencing, Ion Torrent sequencing, and Pacific Biosciences sequencing. It also discusses third generation sequencing and compares the sequencing approaches, workflows, and applications of various sequencing technologies. In conclusion, the document notes the progress and future directions of sequencing, including increased clinical applications and reduced costs.
Structural genomics is a field that aims to determine the 3D structures of all proteins encoded by a genome. It involves determining structures on a large scale using techniques like X-ray crystallography and NMR. This allows identification of novel protein folds and potential drug targets. Comparative genomics compares genomic features between organisms and provides insights into evolution and conserved sequences and functions. It is a key tool in fields like medicine and agriculture.
This document summarizes different computational methods for protein structure prediction, including homology modeling, fold recognition, threading, and ab initio modeling. Homology modeling relies on identifying proteins with similar sequences and known structures. Fold recognition and threading can be used when there are no homologs, to identify proteins with the same overall fold but different sequences. Ab initio modeling uses physics-based modeling and protein fragments to predict structure from sequence alone, and has challenges due to the vast number of possible conformations.
The document discusses several key aspects of gene prediction including:
1. Gene prediction algorithms use signals like start/stop codons, splice sites, and open reading frames to identify genes computationally with near 100% accuracy.
2. There are ab initio, homology-based, and probabilistic models like Hidden Markov Models that can predict prokaryotic and eukaryotic genes.
3. Eukaryotic gene prediction is more challenging due to larger genomes, fewer genes, and intron-exon structures. Programs must consider splicing, polyadenylation, and other post-transcriptional modifications.
Use of reporter genes in the process of selection of the transformants from the non transformants, and the current use of these reporter genes as the Desired genes.
This document discusses different types of sequence alignment methods used in bioinformatics to identify similarities between DNA, RNA, and protein sequences. It describes global and local alignment, which aim to identify conserved regions across entire or local subsequences. Pairwise alignment methods like dot matrix, dynamic programming, and word methods are used to compare two sequences. Multiple sequence alignment extends this to three or more sequences, using progressive, iterative, or dynamic programming approaches to infer evolutionary relationships.
WHAT IS BIOINFORMATICS?
Computational Biology/Bioinformatics is the application of computer sciences and allied technologies to answer the questions of Biologists, about the mysteries of life. It has evolved to serve as the bridge between:
Observations (data) in diverse biologically-related disciplines and
The derivations of understanding (information)
APPLICATIONS OF BIOINFORMATICS
Computer Aided Drug Design
Microarray Bioinformatics
Proteomics
Genomics
Biological Databases
Phylogenetics
Systems Biology
This document discusses the collaboration between molecular medicine and bioinformatics. It defines bioinformatics as the science of storing, retrieving, and analyzing large amounts of biological data, cutting across biology, computer science, and mathematics. It gives examples of how bioinformatics can be applied in molecular medicine for studying pathogenicity, therapeutic targets, molecular diagnostics, and host-pathogen interactions. The document also outlines how bioinformatics supports molecular medicine through genome analysis, database and tool development, and describes some catalysts like genome sequencing that have expanded bioinformatics.
Bioinformatics is the application of computational techniques to analyze and interpret biological data. It involves storing, retrieving, organizing large datasets from molecular biology experiments. Some key developments include the first protein sequence determined in 1955, Needleman-Wunsch algorithm for sequence alignment in 1970, and creation of ARPANET which later became the internet in 1969 allowing for easier sharing of biological data. Bioinformatics now plays an important role in areas like genome sequencing, gene expression analysis, protein structure prediction and molecular evolution studies through analyzing large molecular datasets.
Genomics refers to the study of the entire genome of an organism. It deals with mapping genes on chromosomes and sequencing entire genomes. While work on genomics began with prokaryotes like bacteria, research has now been conducted on crop plants like rice and Arabidopsis thaliana. Genomics is an interdisciplinary field that uses tools from molecular biology, robotics, and computing to study genomes. It provides information on genome size, gene number, gene function, and evolution. Genomics has applications in crop improvement through gene mapping, marker-assisted selection, and transgenic breeding. However, genomic research also faces limitations due to high costs, technical challenges, and complexity of traits.
Introduction
Definition
History
Principle
Components of bioinformatics
Bioinformatics databases
Tools of bioinformatics
Applications of bioinformatics
Molecular medicine
Microbial genomics
Plant genomics
Animal genomics
Human genomics
Drug and vaccine designing
Proteomics
For studying biomolecular structures
In- silico testing
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.
The European Molecular Biology Laboratory (EMBL) is a molecular biology research institution supported by 22 member states. EMBL was created in 1974 and operates from five sites, performing basic research in molecular biology and molecular medicine. A key function of EMBL is the EMBL Nucleotide Sequence Database, maintained at the European Bioinformatics Institute, which incorporates and distributes nucleotide sequences from public sources as part of an international collaboration.
This document summarizes key aspects of sequence alignment. It discusses how sequence alignment involves comparing sequences to find identical or similar characters in the same order. It describes global and local alignment and the algorithms used for each. It also discusses scoring systems for alignments, including penalties for gaps and mismatches. The goals of sequence alignment are to infer functional, structural or evolutionary relationships between sequences.
The study of nucleic acids began with the discovery of DNA, progressed to the study of genes and small fragments, and has now exploded to the field of genomics. Genomics is the study of entire genomes, including the complete set of genes, their nucleotide sequence and organization, and their interactions within a species and with other species. The advances in genomics have been made possible by DNA sequencing technology. [Source: https://opentextbc.ca/biology/chapter/10-3-genomics-and-proteomics/]
description of functional genomics and structural genomics and the techniques involved in it and also decribing the models of forward genetics and techniques involved in it and reverse genetics and techniques involved in it
The document summarizes a bioinformatics summer camp, including:
1. The camp will cover basic molecular biology and bioinformatics topics like DNA, proteins, gene expression and the genetic code.
2. Students will work on computational analysis projects involving whole genome sequencing, gene expression profiling, and functional and comparative genomics.
3. The camp will teach techniques for analyzing protein structures and interactions, gene expression data, and identifying pockets on protein surfaces.
Composite: It compile and filter sequence data from primary database.
Specialized : database—allows targeted searching on one or more specific subject areas
This document discusses genome database systems. It begins with an introduction to bioinformatics and genomes. It then discusses the background of genome databases, including some examples. The major characteristics of genome database systems are described as having high complex data, schema changes at a rapid pace, and complex queries. The key areas of data management in genome databases are discussed as non-standard data, complex queries, data interpretation, integration across databases, and uniform management solutions. Major research areas and applications that impact society are also summarized.
This document provides an overview of DNA sequencing technologies. It begins with a brief history of DNA sequencing, including the discovery of DNA's structure and Sanger sequencing. The document then focuses on next generation sequencing technologies, describing several platforms such as 454 sequencing, Illumina sequencing, Ion Torrent sequencing, and Pacific Biosciences sequencing. It also discusses third generation sequencing and compares the sequencing approaches, workflows, and applications of various sequencing technologies. In conclusion, the document notes the progress and future directions of sequencing, including increased clinical applications and reduced costs.
Structural genomics is a field that aims to determine the 3D structures of all proteins encoded by a genome. It involves determining structures on a large scale using techniques like X-ray crystallography and NMR. This allows identification of novel protein folds and potential drug targets. Comparative genomics compares genomic features between organisms and provides insights into evolution and conserved sequences and functions. It is a key tool in fields like medicine and agriculture.
This document summarizes different computational methods for protein structure prediction, including homology modeling, fold recognition, threading, and ab initio modeling. Homology modeling relies on identifying proteins with similar sequences and known structures. Fold recognition and threading can be used when there are no homologs, to identify proteins with the same overall fold but different sequences. Ab initio modeling uses physics-based modeling and protein fragments to predict structure from sequence alone, and has challenges due to the vast number of possible conformations.
The document discusses several key aspects of gene prediction including:
1. Gene prediction algorithms use signals like start/stop codons, splice sites, and open reading frames to identify genes computationally with near 100% accuracy.
2. There are ab initio, homology-based, and probabilistic models like Hidden Markov Models that can predict prokaryotic and eukaryotic genes.
3. Eukaryotic gene prediction is more challenging due to larger genomes, fewer genes, and intron-exon structures. Programs must consider splicing, polyadenylation, and other post-transcriptional modifications.
Use of reporter genes in the process of selection of the transformants from the non transformants, and the current use of these reporter genes as the Desired genes.
This document discusses different types of sequence alignment methods used in bioinformatics to identify similarities between DNA, RNA, and protein sequences. It describes global and local alignment, which aim to identify conserved regions across entire or local subsequences. Pairwise alignment methods like dot matrix, dynamic programming, and word methods are used to compare two sequences. Multiple sequence alignment extends this to three or more sequences, using progressive, iterative, or dynamic programming approaches to infer evolutionary relationships.
WHAT IS BIOINFORMATICS?
Computational Biology/Bioinformatics is the application of computer sciences and allied technologies to answer the questions of Biologists, about the mysteries of life. It has evolved to serve as the bridge between:
Observations (data) in diverse biologically-related disciplines and
The derivations of understanding (information)
APPLICATIONS OF BIOINFORMATICS
Computer Aided Drug Design
Microarray Bioinformatics
Proteomics
Genomics
Biological Databases
Phylogenetics
Systems Biology
This document discusses the collaboration between molecular medicine and bioinformatics. It defines bioinformatics as the science of storing, retrieving, and analyzing large amounts of biological data, cutting across biology, computer science, and mathematics. It gives examples of how bioinformatics can be applied in molecular medicine for studying pathogenicity, therapeutic targets, molecular diagnostics, and host-pathogen interactions. The document also outlines how bioinformatics supports molecular medicine through genome analysis, database and tool development, and describes some catalysts like genome sequencing that have expanded bioinformatics.
Bioinformatics is the application of computational techniques to analyze and interpret biological data. It involves storing, retrieving, organizing large datasets from molecular biology experiments. Some key developments include the first protein sequence determined in 1955, Needleman-Wunsch algorithm for sequence alignment in 1970, and creation of ARPANET which later became the internet in 1969 allowing for easier sharing of biological data. Bioinformatics now plays an important role in areas like genome sequencing, gene expression analysis, protein structure prediction and molecular evolution studies through analyzing large molecular datasets.
BioInformatics Tools -Genomics , Proteomics and metablomicsAyeshaYousaf20
This document discusses various bioinformatics tools used for genomics, proteomics, and metabolomics. It begins with an introduction to bioinformatics and defines key terms. It then describes several important databases for nucleotide and protein sequences including NCBI, GenBank, and KEGG. Important analytical tools like BLAST and Clustal are also mentioned. Subsequent chapters discuss genomics, proteomics, and metabolomics in more detail and provide examples of specific tools used for each including KNApSAcK, MetaboAnalyst, and PSI-PRED. The document aims to outline the key concepts and computational tools involved in these three areas of bioinformatics.
The document provides an introduction to the field of bioinformatics, including definitions, history, applications and key concepts. It discusses how bioinformatics uses computer algorithms and databases to analyze biological data like genomes, proteins and genes. Major databases that store DNA sequences include GenBank, EMBL and DDBJ. Other databases like PDB contain 3D protein structures. Key applications of bioinformatics include molecular biology, drug design, agriculture and clinical medicine.
The document provides an introduction to the field of bioinformatics, including definitions, history, applications and key concepts. It discusses how bioinformatics uses computer algorithms and databases to analyze biological data like genomes, proteins and genes. Major databases that store DNA sequences are described, such as GenBank, EMBL and DDBJ. Tools for analyzing sequences like BLAST are also introduced.
This document provides an introduction to bioinformatics and biological databases. It defines bioinformatics as the use of computers to analyze biological data like DNA sequences. The aims of bioinformatics include developing databases of all biological information and software for tasks like drug design. Biological databases store complex biological data and can be primary databases containing raw sequences/structures or secondary databases containing derived data. Examples of primary databases include GenBank, EMBL, Swiss-Prot and PDB, while secondary databases include motif, domain, gene expression and metabolic pathway databases. Maintaining accurate, up-to-date biological databases is important for biological research and applications.
Genomics is a discipline in genetics that applies recombinant DNA, DNA sequencing methods, and bioinformatics to sequence, assemble and analyze the function and structure of genomes
Here are some suggestions for open online bioinformatics lectures and courses from famous universities:
- MIT OpenCourseWare has free bioinformatics course materials and videos from MIT courses.
- edX has massive open online courses (MOOCs) in bioinformatics from universities like Harvard, Berkeley, MIT. Some are free to audit.
- Coursera has bioinformatics courses from top universities like Johns Hopkins, University of Toronto, Peking University.
- YouTube has full lecture videos from bioinformatics courses at universities like Stanford, UC San Diego, University of Cambridge.
- Khan Academy has introductory bioinformatics lectures on topics like sequence alignment, gene finding, protein structure.
- EMBL-
This document provides an overview of bioinformatics. It defines bioinformatics as the science of collecting, analyzing and conceptualizing biological data through computational techniques. It discusses that bioinformatics involves managing, organizing and processing biological information from databases, as well as analyzing, visualizing and sharing biological data over the internet. It also outlines some of the goals of bioinformatics like organizing the human and mouse genomes, as well as some applications like genomic and protein sequence analysis, protein structure prediction, and characterizing genomes.
This document provides an overview of bioinformatics. It begins by explaining how bioinformatics emerged from the need to analyze vast amounts of genetic sequence data produced by projects like the Human Genome Project. It then defines bioinformatics as the field that develops tools and methods for understanding biological data by combining computer science, statistics, and other disciplines. The document outlines several goals and applications of bioinformatics, such as identifying genes and their functions, modeling protein structures, comparing genomes, and its uses in medicine, microbial research, and more. It also provides a brief history of important developments in bioinformatics and DNA sequencing.
Bioinformatics is an interdisciplinary field that combines biology, computer science, and information technology. It involves the electronic storage, retrieval, analysis, and correlation of biological data. The document outlines key concepts in bioinformatics including the central dogma of molecular biology, biological data representation, how computers can be useful for biology, challenges in the field, and examples of intelligent bioinformatics applications. It emphasizes that bioinformatics is an important and growing field at the intersection of biology and computer science.
The document discusses bioinformatics tools used for analyzing biological data. It begins with an introduction to bioinformatics and then describes several categories of tools: biological databases for storing genomic and protein data; homology tools for sequence alignment and comparison; protein function analysis tools; structural analysis tools; and sequence manipulation and analysis tools. Common tools discussed include BLAST, FASTA, ClustalW, and databases like GenBank. The document concludes by covering applications of bioinformatics in areas like molecular modeling, medicine, and computation.
introduction,history scope and applications of
relation to other fields , bioinformatics,biological databases,computers internet,sequence development, and
introduction to sequence development and alignment
Bioinformatics is the application of information technology to analyze biological data. This document provides an overview of bioinformatics, including publicly available genome sequences from 1998, promises for applications in medicine and biotechnology, the need for bioinformaticians to analyze growing biological databases, common bioinformatics tasks like sequence analysis and molecular modeling, and important databases like GenBank, SwissProt, and NCBI.
Bioinformatics for beginners (exam point of view)Sijo A
. The term bioinformatics is coined by…………………………….
Paulien Hogeweg
2. What is an entry in database?
The process of entering data into a computerised database or spreadsheet.
3. Define BLASTp
BLAST- Basic Local Alignment Search Tool
It is a homology and similarity search tool.
It is provided by NCBI.
It is used to compare a query DNA sequence with a database of sequences.
4. What is Ecogenes?
Ecogene is a database and website and it is developed to improve structural and functional annotation of E.coli K-12 MG 1655.
This document discusses various bioinformatics tools and their functions. It provides details on multiple sequence alignment tools like CLUSTAL Omega, CLUSTALW, BLAST, and FASTA. It explains that CLUSTAL Omega can align a large number of sequences quickly and accurately using progressive alignment. CLUSTALW performs multiple sequence alignment in three steps - pairwise alignment, guide tree creation, and multiple alignment using the guide tree. BLAST can identify unknown sequences by comparing them to known sequences. FASTA uses short exact matches to find similar regions between sequences. Expasy provides access to databases for proteomics, genomics, and other areas. MASCOT searches peptide mass fingerprinting and shotgun proteomics datasets.
Bioinformatics is the application of computational tools and techniques to analyze and interpret biological data. It involves the development of these tools and databases, as well as their application to better understand biological systems and functions at the molecular level through analysis of genetic sequences, protein structures, and more. The goal is to gain a global understanding of cellular functions by analyzing genetic data as dictated by the central dogma of biology, and relating sequence information to protein functions and cellular processes.
Role of bioinformatics in life sciences researchAnshika Bansal
1. The document discusses bioinformatics and summarizes some of its key applications and tools. It describes how bioinformatics merges biology and computer science to solve biological problems by applying computational tools to molecular data.
2. It provides examples of common bioinformatics tasks like retrieving sequences from databases, comparing sequences, analyzing genes and proteins, and viewing 3D structures.
3. The document lists several popular databases for nucleotide sequences, protein sequences, literature, and other biological data. It also introduces common bioinformatics tools for tasks like sequence alignment, translation, and structure analysis.
The debris of the ‘last major merger’ is dynamically youngSérgio Sacani
The Milky Way’s (MW) inner stellar halo contains an [Fe/H]-rich component with highly eccentric orbits, often referred to as the
‘last major merger.’ Hypotheses for the origin of this component include Gaia-Sausage/Enceladus (GSE), where the progenitor
collided with the MW proto-disc 8–11 Gyr ago, and the Virgo Radial Merger (VRM), where the progenitor collided with the
MW disc within the last 3 Gyr. These two scenarios make different predictions about observable structure in local phase space,
because the morphology of debris depends on how long it has had to phase mix. The recently identified phase-space folds in Gaia
DR3 have positive caustic velocities, making them fundamentally different than the phase-mixed chevrons found in simulations
at late times. Roughly 20 per cent of the stars in the prograde local stellar halo are associated with the observed caustics. Based
on a simple phase-mixing model, the observed number of caustics are consistent with a merger that occurred 1–2 Gyr ago.
We also compare the observed phase-space distribution to FIRE-2 Latte simulations of GSE-like mergers, using a quantitative
measurement of phase mixing (2D causticality). The observed local phase-space distribution best matches the simulated data
1–2 Gyr after collision, and certainly not later than 3 Gyr. This is further evidence that the progenitor of the ‘last major merger’
did not collide with the MW proto-disc at early times, as is thought for the GSE, but instead collided with the MW disc within
the last few Gyr, consistent with the body of work surrounding the VRM.
When I was asked to give a companion lecture in support of ‘The Philosophy of Science’ (https://shorturl.at/4pUXz) I decided not to walk through the detail of the many methodologies in order of use. Instead, I chose to employ a long standing, and ongoing, scientific development as an exemplar. And so, I chose the ever evolving story of Thermodynamics as a scientific investigation at its best.
Conducted over a period of >200 years, Thermodynamics R&D, and application, benefitted from the highest levels of professionalism, collaboration, and technical thoroughness. New layers of application, methodology, and practice were made possible by the progressive advance of technology. In turn, this has seen measurement and modelling accuracy continually improved at a micro and macro level.
Perhaps most importantly, Thermodynamics rapidly became a primary tool in the advance of applied science/engineering/technology, spanning micro-tech, to aerospace and cosmology. I can think of no better a story to illustrate the breadth of scientific methodologies and applications at their best.
Current Ms word generated power point presentation covers major details about the micronuclei test. It's significance and assays to conduct it. It is used to detect the micronuclei formation inside the cells of nearly every multicellular organism. It's formation takes place during chromosomal sepration at metaphase.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
PPT on Direct Seeded Rice presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
ESPP presentation to EU Waste Water Network, 4th June 2024 “EU policies driving nutrient removal and recycling
and the revised UWWTD (Urban Waste Water Treatment Directive)”
ESA/ACT Science Coffee: Diego Blas - Gravitational wave detection with orbita...Advanced-Concepts-Team
Presentation in the Science Coffee of the Advanced Concepts Team of the European Space Agency on the 07.06.2024.
Speaker: Diego Blas (IFAE/ICREA)
Title: Gravitational wave detection with orbital motion of Moon and artificial
Abstract:
In this talk I will describe some recent ideas to find gravitational waves from supermassive black holes or of primordial origin by studying their secular effect on the orbital motion of the Moon or satellites that are laser ranged.
The cost of acquiring information by natural selectionCarl Bergstrom
This is a short talk that I gave at the Banff International Research Station workshop on Modeling and Theory in Population Biology. The idea is to try to understand how the burden of natural selection relates to the amount of information that selection puts into the genome.
It's based on the first part of this research paper:
The cost of information acquisition by natural selection
Ryan Seamus McGee, Olivia Kosterlitz, Artem Kaznatcheev, Benjamin Kerr, Carl T. Bergstrom
bioRxiv 2022.07.02.498577; doi: https://doi.org/10.1101/2022.07.02.498577
20240520 Planning a Circuit Simulator in JavaScript.pptx
Bioinformatics seminar
1. University of Agricultural Sciences, Dharwad
College of Agriculture, Vijayapur
Bioinformatics: An overview and its applications
Department of Biotechnology
Master’s seminar I
15. U A C U G C C U A G U C G
mRNA
Transcriptomics
12
16. U A C U G C C U A G U C G
Proteomics
U A C U G C C U A G U C G
mRNA
Ribosome
Protein
10 20 30 structural
info
12
17. U A C U G C C U A G U C G
Metabolomics
U A C U G C C U A G U C G
mRNA
Ribosome
Metabolic pathway
Biochemical
reactions
and
pathway
Protein
Metabolites
(Enzyme)
12
33. NCBI
(National Center for Biotechnology Information)
• The establishment of the National Center for Biotechnology Information (NCBI) in
November of 1988 occurred primarily through the convergence of three independent
but related actions. They were:
➢1984-86
➢1986
➢1987
24
34. 25
1980: EMBL established their data library.
1981: DNA Databank was established by Japan.
1986: The SWISS-PROT database created.
1988: NCBI was created at NIM/NLH.
1990: BLAST is a fast sequence similarity searching.
1990: The Human Genome Project was started in 1990,
By (1991) a total of 1879 human genes had been mapped
1991:ENTREZ is a search and retrieval tool for NCBI’s linked databases introduced in CD form.
1995:GENOMES provides information on genomes, including sequences, maps,
chromosomes, assembles and annotations.
1997: PubMed is a freely accessible bibliographic retrieval system
to the entire MEDLINE database
2001: Bookshelf is the new ENTREZ database introduced to provide free access to books and
documents in life sciences and health care field.
35. Formulated functions of NCBI were:
• Design, develop, implement, and manage automated systems for the collection, storage, retrieval,
analysis, and dissemination of knowledge concerning human molecular biology, biochemistry,
and genetics;
• Perform research into advanced methods of computer-based information processing capable of
representing and analyzing the vast number of biologically important molecules and compounds;
• Enable persons engaged in biotechnology research and medical care to use systems developed
under paragraph and methods described in paragraph; and
• Coordinate, as much as is practicable, efforts to gather biotechnology information on an
international basis.
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36. The GenBank sequence format is a rich
format for storing sequences and
associated annotations.
Begins with single-line description,
followed by lines of sequence data.
✓ Description line is distinguished
from the sequence data by “>”
symbol.
✓ All lines of text be shorter than 80
characters in length.
✓ Blank lines are not allowed in the
middle of FASTA input.
Sequence Formats
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37. Major categories of Bioinformatics Tools
✤ Homology and Similarity Tools
✤ Protein Function Analysis
✤Structural Analysis
Tools used in Bioinformatics
✤ Sequence Analysis
BLAST
EMBOSS
RasMol
PROSPECT
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41. Phylogenetic trees are genealogical trees which are built up with information
gained from the comparison of the amino acid sequences of a protein like
cytochrome C, sampled from different species.
Phylogenetic trees
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42. !42
How do we identify a gene in a genome?
A gene is characterized by several features (promoter, ORF…)
some are easier and some harder to detect…
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49. Efforts were made to develop a database, PMDBase(Plant Microsatellite DNA
Database), which integrates large amounts of microsatellite DNAs and web service
for its identification.
In PMDBase, 26 230 099 microsatellite DNAs were identified spanning 110 plant
species.
They also developed MISAweb and embedded Primer3web to help users to identify
microsatellite DNAs and design corresponding primers.
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50. Workflow of PMD Base development
Analysis pipeline for generating
microsatellite DNAs
Structure of PMD Base.
Implementation of PMD Base
Yu et al., 2016
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51. Above is a schematic outlining how scientists can use bioinformatics to aid rational drug
discovery. Given the nucleotide sequence, the probable amino acid sequence of the
encoded protein can be determined using translation software. Sequence search techniques
can be used to find homologues in model organisms, and based on sequence similarity, it is
possible to model the structure of the human protein on experimentally characterised
structures.
Luscombe et al., 2000
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54. Stumbling blocks in Bioinformatics:
• Very expensive to use.
• It rare instances it is possible for the algorithm to make mistakes altering
the final result.
• Loss of privacy (Genetic Screening).
• Discrimination from the health insurance companies due to having a certain
genetic disorder revealed through genetic sequencing.
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