Difference between revisions of "MSigDB collections"
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<p>A number of these gene sets come in pairs: an xxx_UP (xxx_DN) gene set representing genes induced (repressed) by the perturbation.<p> | <p>A number of these gene sets come in pairs: an xxx_UP (xxx_DN) gene set representing genes induced (repressed) by the perturbation.<p> | ||
<p>Names of CGP sets start with the last name of the first author of the source publication. The majority of CGP sets were curated from publications and include links to the [http://www.ncbi.nlm.nih.gov/pubmed PubMed] citation, the exact source of the set (e.g., Table 1) and links to the corresponding raw data in [http://www.ncbi.nlm.nih.gov/geo/ GEO] or [http://www.ebi.ac.uk/arrayexpress/ ArrayExpress] repositories. When the set involves a genetic perturbation, brief description includes a link to the gene's entry in the NCBI [http://www.ncbi.nlm.nih.gov/gene Entrez Gene] database. When the set involves a chemical perturbation, brief description includes a link to the chemical's entry in the NCBI [ PubChem Compound] database. | <p>Names of CGP sets start with the last name of the first author of the source publication. The majority of CGP sets were curated from publications and include links to the [http://www.ncbi.nlm.nih.gov/pubmed PubMed] citation, the exact source of the set (e.g., Table 1) and links to the corresponding raw data in [http://www.ncbi.nlm.nih.gov/geo/ GEO] or [http://www.ebi.ac.uk/arrayexpress/ ArrayExpress] repositories. When the set involves a genetic perturbation, brief description includes a link to the gene's entry in the NCBI [http://www.ncbi.nlm.nih.gov/gene Entrez Gene] database. When the set involves a chemical perturbation, brief description includes a link to the chemical's entry in the NCBI [ PubChem Compound] database. | ||
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<li>Sets curated from biomedical literature | <li>Sets curated from biomedical literature | ||
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<li>curated by the MSigDB curation team</li> | <li>curated by the MSigDB curation team</li> | ||
− | </ | + | <li>contributed by L2L</li> |
+ | <p>Sets kindly shared by the [http://depts.washington.edu/l2l/ L2L] database of published microarray gene expression data (described in [http://genomebiology.com/2005/6/9/R81 Newman and Weiner]). These sets list John Newman as the contributor.</p> | ||
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</li> | </li> | ||
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<li>Sets contributed by Dr. Chi Dang from the [http://www.myccancergene.org/site/mycTargetDB.asp MYC Target Gene Database].</li> | <li>Sets contributed by Dr. Chi Dang from the [http://www.myccancergene.org/site/mycTargetDB.asp MYC Target Gene Database].</li> | ||
<li>Individual gene set compilations contributed by MSigDB collaborators. These sets usually are not based on any specific publication.</li> | <li>Individual gene set compilations contributed by MSigDB collaborators. These sets usually are not based on any specific publication.</li> | ||
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<h3>CP: canonical pathways</h3> | <h3>CP: canonical pathways</h3> |
Revision as of 15:17, 7 March 2014
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This page provides detailed descriptions of all collections of gene sets in MSigDB.
To learn about changes and other information specific for a particular release of MSigDB, please refer to the corresponding Release_Notes.
Contents
H: Hallmarks
some text
C1: positional gene sets
Genes from the same genomic location (chromosome or cytogenetic band) are grouped in a gene set. Cytogenetic annotations are from three sources:
- Human Genome Organization (HUGO) Gene Nomenclature Committee (HGNC)
- UniGene
- Affymetrix microarray annotations
We merged the relevant annotations from these resources and derived a single cytogenetic band location for every gene symbol. These were then grouped into sets. Decimals in cytogenetic bands were ignored. For example, 5q31.1 was considered 5q31. Therefore, genes annotated as 5q31.2 and those annotated as 5q31.3 were both placed in the same set, 5q31.
When there were conflicts, the UniGene entry was used.
These sets are helpful in identifying effects related to chromosomal deletions or amplifications, dosage compensation, epigenetic silencing, and other regional effects.
C2: curated gene sets
Gene sets collected from various sources such as online pathway databases, scientific publications and personal contributions from domain experts.
CGP: chemical and genetic perturbations
Over the past few years, microarray studies have identified signatures of several important biological and clinical states (e.g. cancer metastasis, stem cell characteristics, drug resistance). These gene sets are valuable biological results. Unfortunately, because gene sets are typically published as tables in a paper, the important biological findings they represent are not easily accessible to computational tools. Our first goal was to convert published gene sets into an electronic form. Towards this we compiled a list of microarray articles with published gene expression signatures. From each article, we extracted one or more gene sets from tables in the main text or supplementary information. Notably, our focus was on capturing the identity (e.g. gene symbol, GenBank accession) of all members in a gene set rather than on relationships between individual genes.
A number of these gene sets come in pairs: an xxx_UP (xxx_DN) gene set representing genes induced (repressed) by the perturbation.
Names of CGP sets start with the last name of the first author of the source publication. The majority of CGP sets were curated from publications and include links to the PubMed citation, the exact source of the set (e.g., Table 1) and links to the corresponding raw data in GEO or ArrayExpress repositories. When the set involves a genetic perturbation, brief description includes a link to the gene's entry in the NCBI Entrez Gene database. When the set involves a chemical perturbation, brief description includes a link to the chemical's entry in the NCBI [ PubChem Compound] database.
- Sets curated from biomedical literature
- curated by the MSigDB curation team
- contributed by L2L
Sets kindly shared by the L2L database of published microarray gene expression data (described in Newman and Weiner). These sets list John Newman as the contributor.
- Sets contributed by Dr. Chi Dang from the MYC Target Gene Database.
- Individual gene set compilations contributed by MSigDB collaborators. These sets usually are not based on any specific publication.
CP: canonical pathways
Gene sets from the pathway databases. Usually, these gene sets are canonical representations of a biological process compiled by domain experts.
C3: motif gene sets
Gene sets group genes by cis-regulatory motifs. The motifs are catalogued in Xie et al. and represent known or putative conserved regulatory elements in promoters and 3’-UTR regions. These sets make it possible to link changes in a genomic experiment to a conserved, putative cis-regulatory elements.
Transcription factor targets (TFT)
These sets share upstream cis-regulatory motifs which can function as potential transcripton factor binding sites. We used two approaches to generate these gene sets.
Motif gene sets of ‘conserved instances’ consist of the inferred target genes for each motif m of 174 upstream motifs highly conserved among five mammalian species (H. sapiens, M. musculus, R. norvegicus and C. lupus familiaris). The motifs are catalogued in Xie, et al. (2005, Nature 434, 338–345) and represent potential transcription factor binding sites. Each motif gene set consists of all human genes whose promoters (defined as regions -2kb to +2kb around transcription start site) contained at least one conserved instance of motif m. If the motif’s sequence matched a transcription factor binding site documented in v7.4 TRANSFAC database, then we appended the name of the TRANSFAC binding matrix to the motif sequence in the gene name, e.g.: MOTIFSEQ_FOO, where MOTIFSEQ is the sequence of motif m and FOO is the TRANSFAC matrix name (e.g., V$MIF1_01). The set’s full description in this case is the TRANSFAC entry for the matching matrix. If the motif’s sequence matched no transcription factor binding site from TRANSFAC v.7.4, then we named the set as MOTIFSEQ_UNKNOWN where MOTIFSEQ is the consensus sequence of motif m.
We also extracted 460 mammalian transcriptional regulatory motifs from v7.4 TRANSFAC database. We then generated the motif gene sets consisting of the inferred target genes for each motif. Every such set consists of human genes whose promoters (defined as regions -2kb to +2kb around transcription start site) contain at least one instance of the motif. We named these sets by the corresponding TRANSFAC matrix identifiers, e.g., V$MIF1_01. The set’s full description is the TRANSFAC entry for the matching matrix, in a format described here.
microRNA Targets (MIR)
These gene sets consist of the inferred target gene for each motif m of 221 3'-UTR motifs highly conserved among five mammalian species (H. sapiens, M. musculus, R. norvegicus and C. lupus familiaris). The motifs are catalogued catalogued in Xie, et al. 2005, Nature 434, 338–345 and represent potential microRNA binding sites. Each motif gene set consists of all genes whose 3’-UTR contained at least one conserved instance of motif m.
C4: computational gene sets
Gene sets defined by mining large collections of cancer-oriented genes.
C5: GO gene sets
Gene sets are named by Gene Ontology (GO) terms and contain genes annotated by that term.
C6: oncogenetic signatures
Gene sets represent signatures of cellular pathways which are often dis-regulated in cancer. The majority of signatures were generated directly from microarray data from NCBI GEO or from in house unpublished expression profiling experiments which involved perturbation of known cancer genes. In addition, a small number of oncogenic signatures was curated from scientific publications.
C7: immunologic signatures
Gene sets that represent cell states and perturbations within the immune system. The signatures were generated by manual curation of published studies in human and mouse immunology. For each study, pairwise comparisons of relevant classes were made and genes ranked by mutual information. Gene sets correspond to top or bottom ranking genes (FDR < 0.25 or maximum of 200 genes) for each comparison. This resource is generated as part of the Human Immunology Project Consortium (HIPC).