SettingsGenomics
$1,000 genome
The $1,000 Genome is a term that signals a new era of predictive and personalized medicine where the cost of full genome sequencing an individual or patient drops to $1,000.
The $1,000 Genome is a term that signals a new era of predictive and personalized medicine where the cost of full genome sequencing an individual or patient drops to $1,000.
1000 Genomes Project
The 1000 Genomes Project, launched in January 2008, is an international research effort to establish by far the most detailed catalogue of human genetic variation.
The 1000 Genomes Project, launched in January 2008, is an international research effort to establish by far the most detailed catalogue of human genetic variation.
2R hypothesis
The 2R hypothesis or Ohno's hypothesis, first proposed by Susumu Ohno in 1970, is a contested hypothesis in genomics and molecular evolution suggesting that the genomes of the early verteb...
The 2R hypothesis or Ohno's hypothesis, first proposed by Susumu Ohno in 1970, is a contested hypothesis in genomics and molecular evolution suggesting that the genomes of the early verteb...
Activity-based proteomics
Activity based proteomics, or activity based protein profiling (ABPP) is a functional proteomic technology that uses specially designed chemical probes that react with mechanisticall...
Activity based proteomics, or activity based protein profiling (ABPP) is a functional proteomic technology that uses specially designed chemical probes that react with mechanisticall...
Aevol
Aevol is a digital genetics model that was developed to study the evolution of genome structure.
Aevol is a digital genetics model that was developed to study the evolution of genome structure.
Allen Brain Atlas
The Allen Mouse and Brain Atlases are projects within the Allen Institute for Brain Science which seek to combine genomics with neuroanatomy by creating gene expression maps for the mouse and hu...
The Allen Mouse and Brain Atlases are projects within the Allen Institute for Brain Science which seek to combine genomics with neuroanatomy by creating gene expression maps for the mouse and hu...
Alloenzyme
Alloenzymes are common biological enzymes that exhibit high levels of functional evolutionary conservation throughout specific phylas and kingdoms.
Alloenzymes are common biological enzymes that exhibit high levels of functional evolutionary conservation throughout specific phylas and kingdoms.
AlloMap Molecular Expression Testing
AlloMap molecular expression testing, developed and commercialized by XDx, is a gene expression profiling test to identify heart transplant recipients with a low probability of one type of tran...
AlloMap molecular expression testing, developed and commercialized by XDx, is a gene expression profiling test to identify heart transplant recipients with a low probability of one type of tran...
AlloMap molecular expression testing
AlloMap molecular expression testing, developed and commercialized by XDx, is a gene expression profiling test to identify heart transplant recipients with a low probability of one type of tran...
AlloMap molecular expression testing, developed and commercialized by XDx, is a gene expression profiling test to identify heart transplant recipients with a low probability of one type of tran...
Archon X Prize
The Archon X Prize for Genomics, the second X Prize to be offered by the X Prize Foundation, based in Santa Monica, California, was announced on October 4, 2006.
The Archon X Prize for Genomics, the second X Prize to be offered by the X Prize Foundation, based in Santa Monica, California, was announced on October 4, 2006.
Autonomously replicating sequence
An autonomously replicating sequence (ARS) contains the origin of replication in the yeast genome.
An autonomously replicating sequence (ARS) contains the origin of replication in the yeast genome.
Bacterial genome size
Bacterial genomes are generally smaller and less variant in size between species when compared with genomes of animals and single cell eukaryotes.
Bacterial genomes are generally smaller and less variant in size between species when compared with genomes of animals and single cell eukaryotes.
Biochip
The development of biochips is a major thrust of the rapidly growing biotechnology industry, which encompasses a very diverse range of research efforts including genomics, proteomics, and pharma...
The development of biochips is a major thrust of the rapidly growing biotechnology industry, which encompasses a very diverse range of research efforts including genomics, proteomics, and pharma...
Bisulfite sequencing
Bisulfite sequencing (also known as bisulphite sequencing) is the use of bisulfite treatment of DNA to determine its pattern of methylation.
Bisulfite sequencing (also known as bisulphite sequencing) is the use of bisulfite treatment of DNA to determine its pattern of methylation.
C3orf14-Chromosome 3 open reading frame 14
New article name is C3orf14-Chromosome 3 Open Reading Frame 14 Chromosome 3 open reading frame 14 is a gene of uncertain function located at 3p14.2 near fragile site FRBA3—which falls between th...
New article name is C3orf14-Chromosome 3 Open Reading Frame 14 Chromosome 3 open reading frame 14 is a gene of uncertain function located at 3p14.2 near fragile site FRBA3—which falls between th...
Cancer genome sequencing
Cancer genome sequencing is the whole genome sequencing of a single, homogeneous or heterogeneous group of cancer cells.
Cancer genome sequencing is the whole genome sequencing of a single, homogeneous or heterogeneous group of cancer cells.
Catfish genome database
The catfish genome database (cBARBEL) is a database for the genetics of Ictalurus spp.
The catfish genome database (cBARBEL) is a database for the genetics of Ictalurus spp.
Center for Bioinformatics and Computational Biology
The Center for Bioinformatics and Computational Biology (CBCB) is a University of Maryland, College Park multidisciplinary center dedicated to research on questions arising from the genome revol...
The Center for Bioinformatics and Computational Biology (CBCB) is a University of Maryland, College Park multidisciplinary center dedicated to research on questions arising from the genome revol...
Center for Genomics and Healthcare Equality
The Center for Genomics and Healthcare Equality, was founded in the United States 2004 as one of the National Human Genome Research Institute established Centers for Excellence for research into...
The Center for Genomics and Healthcare Equality, was founded in the United States 2004 as one of the National Human Genome Research Institute established Centers for Excellence for research into...
CG suppression
CG suppression is a term for the phenomenon that CG dinucleotides are very uncommon in most portions of vertebrate genomes.
CG suppression is a term for the phenomenon that CG dinucleotides are very uncommon in most portions of vertebrate genomes.
Chemogenomics
Chemogenomics is the study of genomic responses to chemical compounds.
Chemogenomics is the study of genomic responses to chemical compounds.
ChIP-exo
ChIP-exo is a chromatin immunoprecipitation based method for mapping the locations at which a protein of interest (transcription factor) binds to the genome.
ChIP-exo is a chromatin immunoprecipitation based method for mapping the locations at which a protein of interest (transcription factor) binds to the genome.
Chordate genomics
Chordate genomics is the study of the evolution of the chordate clade based on a comparison of the genomes of several species within the clade.
Chordate genomics is the study of the evolution of the chordate clade based on a comparison of the genomes of several species within the clade.
CIT Program Tumor Identity Cards
The "Cartes d'Identité des Tumeurs (CIT)" program (or 'Tumor Identity Cards'), launched and financed by the French charity "Ligue Nationale contre le Cancer", aims at characterizing multiple typ...
The "Cartes d'Identité des Tumeurs (CIT)" program (or 'Tumor Identity Cards'), launched and financed by the French charity "Ligue Nationale contre le Cancer", aims at characterizing multiple typ...
Clinomics
Clinomics is the study of -omics data along with its associated clinical data.
Clinomics is the study of -omics data along with its associated clinical data.
Cofactor Genomics
Cofactor Genomics is a Missouri based firm which provides full genome sequencing, DNA sequencing, RNA sequencing, De Novo sequence assembly, expressed sequence tagging, gene alignments and seque...
Cofactor Genomics is a Missouri based firm which provides full genome sequencing, DNA sequencing, RNA sequencing, De Novo sequence assembly, expressed sequence tagging, gene alignments and seque...
Cognitive Genomics
Cognitive Genomics is the sub-field of genomics pertaining to cognitive function in which the genes and non-coding sequences of an organism's genome related to the health and activity of the bra...
Cognitive Genomics is the sub-field of genomics pertaining to cognitive function in which the genes and non-coding sequences of an organism's genome related to the health and activity of the bra...
Combrex
COMBREX is a database of functional predictions of prokaryotic genomes COMBREX is a multifaceted project that aims to bring together the computational and experimental communities of biologis...
COMBREX is a database of functional predictions of prokaryotic genomes COMBREX is a multifaceted project that aims to bring together the computational and experimental communities of biologis...
Comparative genomics
Comparative genomics is the study of the relationship of genome structure and function across different biological species or strains.
Comparative genomics is the study of the relationship of genome structure and function across different biological species or strains.
Computational genomics
Computational genomics refers to the use of computational analysis to decipher biology from genome sequences and related data, including both DNA and RNA sequence as well as other "post-genomic"...
Computational genomics refers to the use of computational analysis to decipher biology from genome sequences and related data, including both DNA and RNA sequence as well as other "post-genomic"...
Contig
A contig (from contiguous) is a set of overlapping DNA segments that together represent a consensus region of DNA.
A contig (from contiguous) is a set of overlapping DNA segments that together represent a consensus region of DNA.
Convergent Functional Genomics (CFG)
Convergent Functional Genomics Developed by Alexander Niculescu, MD, PhD, and collaborators starting in 1999, it is an approach for identifying and prioritizing candidate genes and biomarkers ...
Convergent Functional Genomics Developed by Alexander Niculescu, MD, PhD, and collaborators starting in 1999, it is an approach for identifying and prioritizing candidate genes and biomarkers ...
CoRR hypothesis
The CoRR hypothesis states that the location of genetic information in cytoplasmic organelles permits regulation of its expression by the reduction-oxidation ("redox") state of its gene products.
The CoRR hypothesis states that the location of genetic information in cytoplasmic organelles permits regulation of its expression by the reduction-oxidation ("redox") state of its gene products.
Disease gene identification
Disease gene identification is a process by which scientists identify the mutant genotypes responsible for an inherited genetic disorder.
Disease gene identification is a process by which scientists identify the mutant genotypes responsible for an inherited genetic disorder.
DNA Data Bank of Japan
The DNA Data Bank of Japan is a biological database that collects DNA sequences.
The DNA Data Bank of Japan is a biological database that collects DNA sequences.
E1b1b1b
In human genetics, E1b1b1b, is the name of a major Y chromosome haplogroup found in North Africa, Western Asia and Europe.
In human genetics, E1b1b1b, is the name of a major Y chromosome haplogroup found in North Africa, Western Asia and Europe.
E1b1b1b (Y-DNA)
In human genetics, E1b1b1b (or E-V257), is the name of a major Y chromosome haplogroup mainly found in North Africa and to a lesser extent in Western Asia and Europe.
In human genetics, E1b1b1b (or E-V257), is the name of a major Y chromosome haplogroup mainly found in North Africa and to a lesser extent in Western Asia and Europe.
ECRbase
ECRbase is a database of evolutionary conserved regions, promoters, and transcription factor binding sites, in vertebrate genomes.
ECRbase is a database of evolutionary conserved regions, promoters, and transcription factor binding sites, in vertebrate genomes.
Epigenomics
Epigenomics deals with "Genomics maps of stable, yet reprogrammable nuclear changes that control gene expression and influence our health".
Epigenomics deals with "Genomics maps of stable, yet reprogrammable nuclear changes that control gene expression and influence our health".
Exogenote
An exogenote is a DNA donor, usually occurs in mating of prokaryotic organisms.
An exogenote is a DNA donor, usually occurs in mating of prokaryotic organisms.
Expressed sequence tag
An expressed sequence tag or EST is a short sub-sequence of a transcribed cDNA sequence.
An expressed sequence tag or EST is a short sub-sequence of a transcribed cDNA sequence.
Fiocruz Genome Comparison Project
The Fiocruz Genome Comparison Project is a collaborative effort involving Brazil's Oswaldo Cruz Institute and IBM's World Community Grid, designed to produce a database comparing the genes from ...
The Fiocruz Genome Comparison Project is a collaborative effort involving Brazil's Oswaldo Cruz Institute and IBM's World Community Grid, designed to produce a database comparing the genes from ...
Full genome sequencing
Full genome sequencing (FGS), also known as whole genome sequencing, complete genome sequencing, or entire genome sequencing, is a laboratory process that determines the comple...
Full genome sequencing (FGS), also known as whole genome sequencing, complete genome sequencing, or entire genome sequencing, is a laboratory process that determines the comple...
Functional genomics
Functional genomics is a field of molecular biology that attempts to make use of the vast wealth of data produced by genomic projects (such as genome sequencing projects) to describe gene (and ...
Functional genomics is a field of molecular biology that attempts to make use of the vast wealth of data produced by genomic projects (such as genome sequencing projects) to describe gene (and ...
GDB Human Genome Database
The GDB Human Genome Database was a community curated collection of human genomic data.
The GDB Human Genome Database was a community curated collection of human genomic data.
GEN2PHEN
Genotype to Phenotype Databases: a Holistic Approach is a European project aiming to develop a knowledge web portal integrating information from the genotype to the phenotype in a unifying porta...
Genotype to Phenotype Databases: a Holistic Approach is a European project aiming to develop a knowledge web portal integrating information from the genotype to the phenotype in a unifying porta...
GeneCalling
GeneCalling is a mRNA profiling technology finding increased use in the field of genomics and invented by Dr. Jonathan M. Rothberg and developed by CuraGen Corporation.
GeneCalling is a mRNA profiling technology finding increased use in the field of genomics and invented by Dr. Jonathan M. Rothberg and developed by CuraGen Corporation.
GeneDx
GeneDx is genetic testing company that was founded in 2000 by two scientists from the National Institutes of Health (NIH), Drs.
GeneDx is genetic testing company that was founded in 2000 by two scientists from the National Institutes of Health (NIH), Drs.
GeneMark
GeneMark is a family of gene prediction programs developed at the Georgia Institute of Technology in Atlanta.
GeneMark is a family of gene prediction programs developed at the Georgia Institute of Technology in Atlanta.
Generic Model Organism Database
The Generic Model Organism Database (GMOD) Project began as an effort to create reusable software tools for developing Model Organism Databases (MODs).
The Generic Model Organism Database (GMOD) Project began as an effort to create reusable software tools for developing Model Organism Databases (MODs).
GeneRIF
A GeneRIF or Gene Reference Into Function is a short statement about the function of a gene.
A GeneRIF or Gene Reference Into Function is a short statement about the function of a gene.
Genome
In modern molecular biology and genetics, the genome is the entirety of an organism's hereditary information.
In modern molecular biology and genetics, the genome is the entirety of an organism's hereditary information.
Genome Biology
Genome Biology is an online partially open access scientific journal that publishes original, peer-reviewed research in genomics.
Genome Biology is an online partially open access scientific journal that publishes original, peer-reviewed research in genomics.
Genome browser
A genome browser is a graphical interface for display of information from a biological database for genomic data.
A genome browser is a graphical interface for display of information from a biological database for genomic data.
Genome engineering
Genome engineering refers to the strategies and techniques developed in recent years for the targeted, specific modification of the genetic information – or genome – of living organisms.
Genome engineering refers to the strategies and techniques developed in recent years for the targeted, specific modification of the genetic information – or genome – of living organisms.
Genome Research Foundation
Genome Research Foundation also known as Genome Foundation is a non-profit research foundation and institute in Korea under the approval of the ministry of Education, Science, and Technology of ...
Genome Research Foundation also known as Genome Foundation is a non-profit research foundation and institute in Korea under the approval of the ministry of Education, Science, and Technology of ...
Genomic counseling
Genomic counseling is the process by which a person gets informed about its genome.
Genomic counseling is the process by which a person gets informed about its genome.
Genomic phylostratigraphy
Genomic phylostratigraphy is a statistical approach for reconstruction of macroevolutionary trends based on the principle of founder gene formation and punctuated emergence of protein families.
Genomic phylostratigraphy is a statistical approach for reconstruction of macroevolutionary trends based on the principle of founder gene formation and punctuated emergence of protein families.
Genomic Standards Consortium
The Genomic Standards Consortium is an initiative working towards richer descriptions of our collection of genomes, metagenomes and marker genes.
The Genomic Standards Consortium is an initiative working towards richer descriptions of our collection of genomes, metagenomes and marker genes.
Genomics
Genomics is a discipline in genetics concerning the study of the genomes of organisms.
Genomics is a discipline in genetics concerning the study of the genomes of organisms.
GenoMik
GenoMik - genome research on microorganisms is a program for the study of the genome of selected microorganisms.
GenoMik - genome research on microorganisms is a program for the study of the genome of selected microorganisms.
Haplogroup E1b1b (Y-DNA)
In human genetics, Y Haplogroup E1b1b, previously known as E3b, is a major Y-chromosome haplogroup, which is a division of the macro haplogroup E, and which is defined by the single nucleo...
In human genetics, Y Haplogroup E1b1b, previously known as E3b, is a major Y-chromosome haplogroup, which is a division of the macro haplogroup E, and which is defined by the single nucleo...
Haplogroup E1b1b1a (Y-DNA)
In human genetics, E1b1b1a (or E-V68), is the name of a major Y chromosome haplogroup found in North Africa, the Horn of Africa, Western Asia and Europe.
In human genetics, E1b1b1a (or E-V68), is the name of a major Y chromosome haplogroup found in North Africa, the Horn of Africa, Western Asia and Europe.
Haplogroup E1b1b1b (Y-DNA)
In human genetics, E1b1b1b, is the name of a major Y chromosome haplogroup mainly found in North Africa and to a lesser extent in Western Asia and Europe.
In human genetics, E1b1b1b, is the name of a major Y chromosome haplogroup mainly found in North Africa and to a lesser extent in Western Asia and Europe.
Happy mapping
HAPPY Mapping, first proposed by Paul H. Dear and Peter R. Cook in 1989, is a method used in molecular biology to study the linkage between two or more DNA sequences.
HAPPY Mapping, first proposed by Paul H. Dear and Peter R. Cook in 1989, is a method used in molecular biology to study the linkage between two or more DNA sequences.
HCP5
The gene known as HCP5 is a human endogenous retrovirus, meaning that it is a fossil of an ancient virus that at one time infected people, but has now become an integral part of the human genome.
The gene known as HCP5 is a human endogenous retrovirus, meaning that it is a fossil of an ancient virus that at one time infected people, but has now become an integral part of the human genome.
Honey Bee Genome Sequencing Consortium
The Honey Bee Genome Sequencing Consortium is an international collaborative group of genomics scientists, scientific organisations and universities who are trying to decipher the genome sequenc...
The Honey Bee Genome Sequencing Consortium is an international collaborative group of genomics scientists, scientific organisations and universities who are trying to decipher the genome sequenc...
Immunological Genome Project
The Immunological Genome Project (ImmGen) is a collaborative scientific research project that is currently building a gene-expression microarray database for all characterized immune cells in th...
The Immunological Genome Project (ImmGen) is a collaborative scientific research project that is currently building a gene-expression microarray database for all characterized immune cells in th...
Immunoproteomics
Immunoproteomics is a term used to describe the study of large sets of proteins (proteomics) involved in the immune response.
Immunoproteomics is a term used to describe the study of large sets of proteins (proteomics) involved in the immune response.
Institute of Genomics and Integrative Biology
Institute of Genomics and Integrative Biology (IGIB) is a scientific research institute devoted primarily to integrated biological research.
Institute of Genomics and Integrative Biology (IGIB) is a scientific research institute devoted primarily to integrated biological research.
International Grape Genome Program
The International Grape Genomics Program (IGGP) is a collaborative genome project dedicated to determining the genome sequence of the grapevine Vitis vinifera.
The International Grape Genomics Program (IGGP) is a collaborative genome project dedicated to determining the genome sequence of the grapevine Vitis vinifera.
John Quackenbush
John Quackenbush (born January 4, 1962) is an American computational biologist and genome scientist.
John Quackenbush (born January 4, 1962) is an American computational biologist and genome scientist.
Locus Reference Genomic
Locus Reference Genomic (LRG) is a DNA sequence format that was developed to aid in curating locus specific databases (LSDBs) that record DNA sequence variation which can result in inherited dis...
Locus Reference Genomic (LRG) is a DNA sequence format that was developed to aid in curating locus specific databases (LSDBs) that record DNA sequence variation which can result in inherited dis...
Maqsudul Alam
Maqsudul Alam is a Bangladeshi American Scientist and Professor.
Maqsudul Alam is a Bangladeshi American Scientist and Professor.
Materials Genome
The name Materials Genome was coined in December 2002 by Dr. Zi-Kui Liu who incorporated the company "MaterialsGenome, Inc." in Pennsylvania, USA, and filed the trademark protection on March 5, 2004.
The name Materials Genome was coined in December 2002 by Dr. Zi-Kui Liu who incorporated the company "MaterialsGenome, Inc." in Pennsylvania, USA, and filed the trademark protection on March 5, 2004.
Materiomics
Materiomics is defined as the study of the material properties of natural and synthetic materials by examining fundamental links between processes, structures and properties at multiple scales, ...
Materiomics is defined as the study of the material properties of natural and synthetic materials by examining fundamental links between processes, structures and properties at multiple scales, ...
Medicago truncatula
Medicago truncatula is a small legume native to the Mediterranean region that is used in genomic research.
Medicago truncatula is a small legume native to the Mediterranean region that is used in genomic research.
Metabolic network modelling
Metabolic network reconstruction and simulation allows for an in depth insight into comprehending the molecular mechanisms of a particular organism, especially correlating the genome with molecu...
Metabolic network reconstruction and simulation allows for an in depth insight into comprehending the molecular mechanisms of a particular organism, especially correlating the genome with molecu...
Metabolomics
Metabolomics is the scientific study of chemical processes involving metabolites.
Metabolomics is the scientific study of chemical processes involving metabolites.
Metagenomics
Metagenomics is the study of metagenomes, genetic material recovered directly from environmental samples.
Metagenomics is the study of metagenomes, genetic material recovered directly from environmental samples.
Methylated DNA immunoprecipitation
Methylated DNA immunoprecipitation is a large-scale purification technique in molecular biology that is used to enrich for methylated DNA sequences.
Methylated DNA immunoprecipitation is a large-scale purification technique in molecular biology that is used to enrich for methylated DNA sequences.
Molecular Inversion Probe
Molecular Inversion Probe belongs to the class of Capture by Circularization molecular techniques for performing genomic partitioning, a process through which one captures and enrich...
Molecular Inversion Probe belongs to the class of Capture by Circularization molecular techniques for performing genomic partitioning, a process through which one captures and enrich...
Molecular models of DNA
Molecular models of DNA structures are representations of the molecular geometry and topology of Deoxyribonucleic acid molecules using one of several means, with the aim of simplifying and pres...
Molecular models of DNA structures are representations of the molecular geometry and topology of Deoxyribonucleic acid molecules using one of several means, with the aim of simplifying and pres...
Monopartite
Monopartite refers to the class of genome that is presented in the genome of the virus.
Monopartite refers to the class of genome that is presented in the genome of the virus.
Mouse Genome Database
The Mouse Genome Database is database for phenotype and functional annotations of mouse genes.
The Mouse Genome Database is database for phenotype and functional annotations of mouse genes.
Multipartite
Multipartite is a class of virus that have segmented nucleic acid genome.
Multipartite is a class of virus that have segmented nucleic acid genome.
Mycobacterium Tuberculosis Structural Genomics Consortium
The TB Structural Genomics Consortium is a worldwide consortium of scientists developing a foundation for tuberculosis diagnosis and treatment by determining the 3-dimensional structures of prot...
The TB Structural Genomics Consortium is a worldwide consortium of scientists developing a foundation for tuberculosis diagnosis and treatment by determining the 3-dimensional structures of prot...
N50 statistic
In Computational Biology, the N50 statistic is a measure of the average length of a set of sequences, with greater weight given to longer sequences.
In Computational Biology, the N50 statistic is a measure of the average length of a set of sequences, with greater weight given to longer sequences.
National Center for Integrative Biomedical Informatics
The National Center for Integrative Biomedical Informatics (NCIBI) is one of seven National Centers for Biomedical Computing funded by the National Institutes of Health's (NIH) Roadmap for Medic...
The National Center for Integrative Biomedical Informatics (NCIBI) is one of seven National Centers for Biomedical Computing funded by the National Institutes of Health's (NIH) Roadmap for Medic...
National Centers for Biomedical Computing
The National Centers for Biomedical Computing (NCBCs) are part of the U.S. NIH plan to develop and implement the core of a universal computing infrastructure that is urgently needed to speed pro...
The National Centers for Biomedical Computing (NCBCs) are part of the U.S. NIH plan to develop and implement the core of a universal computing infrastructure that is urgently needed to speed pro...
National Institute of Genetics
The National Institute of Genetics is a Japanese institution founded in 1949.
The National Institute of Genetics is a Japanese institution founded in 1949.
Navigenics
Navigenics, Inc. is a privately-held personal genomics company, based in Foster City, California, that uses genetic testing to help people determine their individual risk for dozens of health co...
Navigenics, Inc. is a privately-held personal genomics company, based in Foster City, California, that uses genetic testing to help people determine their individual risk for dozens of health co...
Nutritional genomics
Nutritional genomics is a science studying the relationship between human genome, nutrition and health.
Nutritional genomics is a science studying the relationship between human genome, nutrition and health.
Omics
The English-language neologism omics informally refers to a field of study in biology ending in -omics, such as genomics, proteomics or metabolomics.
The English-language neologism omics informally refers to a field of study in biology ending in -omics, such as genomics, proteomics or metabolomics.
Orphan gene
An orphan gene is a gene that has limited phylogenetic distribution.
An orphan gene is a gene that has limited phylogenetic distribution.
Pan-genome
In molecular biology a pan-genome describes the full complement of genes in a species (typically applied to bacteria and archaea, which can have large variation in gene content among closely rel...
In molecular biology a pan-genome describes the full complement of genes in a species (typically applied to bacteria and archaea, which can have large variation in gene content among closely rel...
Pangenome
pangenome describes the full complement of genes in a species.
pangenome describes the full complement of genes in a species.
Pathogenomics
The study of Pathogenomics attempts to utilize genomic and metagenomics data gathered from high through-put technologies (e.g.
The study of Pathogenomics attempts to utilize genomic and metagenomics data gathered from high through-put technologies (e.g.
Pathway Genomics
Pathway Genomics is a privately held personal genomics company based in San Diego, California.
Pathway Genomics is a privately held personal genomics company based in San Diego, California.
Personal genomics
Personal genomics is the branch of genomics concerned with the sequencing and analysis of the genome of an individual.
Personal genomics is the branch of genomics concerned with the sequencing and analysis of the genome of an individual.
Personalized medicine
Personalized medicine is a medical model that proposes the customization of healthcare, with all decisions and practices being tailored to the individual patient by use of genetic or other infor...
Personalized medicine is a medical model that proposes the customization of healthcare, with all decisions and practices being tailored to the individual patient by use of genetic or other infor...
Pharmacodiagnostic testing
Pharmacodiagnostic testing is pre-treatment testing performed in order to determine whether or not a patient is likely to respond to a given therapy.
Pharmacodiagnostic testing is pre-treatment testing performed in order to determine whether or not a patient is likely to respond to a given therapy.
Pharmacogenomics
Pharmacogenomics is the branch of pharmacology which deals with the influence of genetic variation on drug response in patients by correlating gene expression or single-nucleotide polymorphisms ...
Pharmacogenomics is the branch of pharmacology which deals with the influence of genetic variation on drug response in patients by correlating gene expression or single-nucleotide polymorphisms ...
Phylotype
A phylotype is biological type that classifies an organism by its phylogenetic, that is evolutionary, relationship to other organisms.
A phylotype is biological type that classifies an organism by its phylogenetic, that is evolutionary, relationship to other organisms.
Plant Genome Mapping Laboratory
The Plant Genome Mapping Laboratory (PGML) is a lab affiliated to the University of Georgia, directed by Dr. Andrew H. Paterson.
The Plant Genome Mapping Laboratory (PGML) is a lab affiliated to the University of Georgia, directed by Dr. Andrew H. Paterson.
Population genomics
Population genomics is the large-scale comparison of DNA sequences of populations.
Population genomics is the large-scale comparison of DNA sequences of populations.
Protein Information Resource
The Protein Information Resource, located at Georgetown University Medical Center, is an integrated public bioinformatics resource to support genomic and proteomic research, and scientific studi...
The Protein Information Resource, located at Georgetown University Medical Center, is an integrated public bioinformatics resource to support genomic and proteomic research, and scientific studi...
Proteogenomics
Proteogenomics Proteogenomics is an emerging field of biological research at the intersection of proteomics and genomics.
Proteogenomics Proteogenomics is an emerging field of biological research at the intersection of proteomics and genomics.
Proteome
The proteome is the entire set of proteins expressed by a genome, cell, tissue or organism.
The proteome is the entire set of proteins expressed by a genome, cell, tissue or organism.
Proteomics
Proteomics is the large-scale study of proteins, particularly their structures and functions.
Proteomics is the large-scale study of proteins, particularly their structures and functions.
Public Genomics
Public genomics is a genomics branch that was initiated by public organizations such as governments, discontrol centers, and the UN. Public genomics is effectively the public facet of personal g...
Public genomics is a genomics branch that was initiated by public organizations such as governments, discontrol centers, and the UN. Public genomics is effectively the public facet of personal g...
Public health genomics
Public Health Genomics is the use of genomics information to benefit public health.
Public Health Genomics is the use of genomics information to benefit public health.
Public Population Project in Genomics
P3G (Public Population Project in Genomics) is a not-for-profit international consortium dedicated to facilitating collaboration between researchers and biobanks working in the area ...
P3G (Public Population Project in Genomics) is a not-for-profit international consortium dedicated to facilitating collaboration between researchers and biobanks working in the area ...
Radiogenomics
Radiogenomics involves the correlation of radiology information to genomic data.
Radiogenomics involves the correlation of radiology information to genomic data.
Representational difference analysis
Representational Difference Analysis (RDA) is a technique used in biological research to find sequence differences in two genomic or cDNA samples.
Representational Difference Analysis (RDA) is a technique used in biological research to find sequence differences in two genomic or cDNA samples.
Resistome
The resistome is a proposed expression by Gerard D. Wright for the collection of all the antibiotic resistance genes and their precursors in both pathogenic and non-pathogenic bacteria.
The resistome is a proposed expression by Gerard D. Wright for the collection of all the antibiotic resistance genes and their precursors in both pathogenic and non-pathogenic bacteria.
Restriction fragment length polymorphism
In molecular biology, restriction fragment length polymorphism, or RFLP (commonly pronounced “rif-lip”), is a technique that exploits variations in homologous DNA sequences.
In molecular biology, restriction fragment length polymorphism, or RFLP (commonly pronounced “rif-lip”), is a technique that exploits variations in homologous DNA sequences.
Restriction landmark genomic scanning
Restriction Landmark Genomic Scanning (or RLGS) is a genome analysis method that allows for rapid simultaneous visualization of thousands of landmarks, or restriction sites.
Restriction Landmark Genomic Scanning (or RLGS) is a genome analysis method that allows for rapid simultaneous visualization of thousands of landmarks, or restriction sites.
Ribonomics
Ribonomics is the study of ribonucleic acids (RNAs) associated with RNA-binding proteins (RBPs).
Ribonomics is the study of ribonucleic acids (RNAs) associated with RNA-binding proteins (RBPs).
Ridge (biology)
Ridges (regions of increased gene expression) are domains of the genome with a high gene expression; the opposite of ridges are antiridges.
Ridges (regions of increased gene expression) are domains of the genome with a high gene expression; the opposite of ridges are antiridges.
Scripps Genomic Health Initiative
The Scripps Genomic Health Initiative (SGHI) is a ground-breaking study aimed at understanding how personal genetic testing influences and improves health.
The Scripps Genomic Health Initiative (SGHI) is a ground-breaking study aimed at understanding how personal genetic testing influences and improves health.
Sequence-tagged site
A sequence-tagged site (or STS) is a short (200 to 500 base pair) DNA sequence that has a single occurrence in the genome and whose location and base sequence are known.
A sequence-tagged site (or STS) is a short (200 to 500 base pair) DNA sequence that has a single occurrence in the genome and whose location and base sequence are known.
Single molecule real time sequencing
Single molecule real time sequencing (also known as SMRT) is a parallelized single molecule DNA sequencing by synthesis technology developed by Pacific Biosciences.
Single molecule real time sequencing (also known as SMRT) is a parallelized single molecule DNA sequencing by synthesis technology developed by Pacific Biosciences.
STR analysis
Short tandem repeat (STR) analysis is a molecular biology method used to compare specific loci on DNA from two or more samples.
Short tandem repeat (STR) analysis is a molecular biology method used to compare specific loci on DNA from two or more samples.
Structural genomics
Structural genomics seeks to describe the 3-dimensional structure of every protein encoded by a given genome.
Structural genomics seeks to describe the 3-dimensional structure of every protein encoded by a given genome.
Structural proteomics
Structural proteomics is an international collaboration project for solving 3D protein structures at a proteome scale.
Structural proteomics is an international collaboration project for solving 3D protein structures at a proteome scale.
Subfunctionalization
Subfunctionalization is a model that explains the process by which duplicated genes remain functional in a genome.
Subfunctionalization is a model that explains the process by which duplicated genes remain functional in a genome.
SUPERFAMILY
SUPERFAMILY is a database of structural and functional annotation for all proteins and genomes.
SUPERFAMILY is a database of structural and functional annotation for all proteins and genomes.
Theranostics
Theranostics (a portmanteau of therapeutics and diagnostics) is a proposed process of diagnostic therapy for individual patients - to test them for possible reaction to taking a new medi...
Theranostics (a portmanteau of therapeutics and diagnostics) is a proposed process of diagnostic therapy for individual patients - to test them for possible reaction to taking a new medi...
Toxicogenomics
Toxicogenomics is a field of science that deals with the collection, interpretation, and storage of information about gene and protein activity within particular cell or tissue of an organism in...
Toxicogenomics is a field of science that deals with the collection, interpretation, and storage of information about gene and protein activity within particular cell or tissue of an organism in...
TREC Genomics
The TREC Genomics track was a workshop held under the auspices of NIST for the purpose of evaluating systems for information retrieval and related technologies in the genomics domain.
The TREC Genomics track was a workshop held under the auspices of NIST for the purpose of evaluating systems for information retrieval and related technologies in the genomics domain.
UniFrac
UniFrac is a method to calculate a distance measure between bacterial communities using phylogenetic information, and is widely used in metagenomics.
UniFrac is a method to calculate a distance measure between bacterial communities using phylogenetic information, and is widely used in metagenomics.
VISTA (comparative genomics)
VISTA is a collection of databases, tools, and servers that permit extensive comparative genomics analyses.
VISTA is a collection of databases, tools, and servers that permit extensive comparative genomics analyses.
Whole genome sequencing
Full genome sequencing (FGS), also known as whole genome sequencing (WGS), complete genome sequencing, or entire genome sequencing, is a laboratory process that determines the ...
Full genome sequencing (FGS), also known as whole genome sequencing (WGS), complete genome sequencing, or entire genome sequencing, is a laboratory process that determines the ...