Difference between revisions of "MSigDB v3.1 Release Notes"

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<p>This page describes changes in Release 3.1 of the Molecular Signatures Database (MSigDB)</p>
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[http://www.broadinstitute.org/gsea/ GSEA Home] |
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[http://www.broadinstitute.org/gsea/downloads.jsp Downloads] |
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<h2>New collection C6: Oncogenic Pathway Activation Modules</h2>
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[http://www.broadinstitute.org/gsea/msigdb/ Molecular Signatures Database] |
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[http://www.broadinstitute.org/cancer/software/gsea/wiki/index.php/Main_Page Documentation] |
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<p> <strong>C6: Oncogenic Pathway Activation Modules</strong> is a new collection of <strong>189 gene sets</strong>. These gene sets represent expression signatures derived directly from microarray data from experiments involving gain or loss of function of several established cancer genes in well defined, "clean" experimental systems. In this context, gain of function stands for increased activity of a cancer gene by means of over-expression or treatment with a chemical modulator. Conversely, loss of function stands for diminished activity of the cancer gene by means of RNAi knockdown, gene knockout, or enzymatic inhibition.</p>
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[http://www.broadinstitute.org/gsea/contact.jsp Contact] <br />
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<br />
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<h2>New gene sets in the C2 collection </h2>
 
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<p><strong>The C2: Curated gene sets collection </strong> consists of gene sets collected from various sources such as online pathway databases, publications in PubMed, and knowledge of domain experts. </p>
 
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<ul>
 
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    <li><strong>CGP</strong>: chemical and genetic perturbations <strong>(+1,006)</strong></li>
 
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<p>There are 1,035 new sets curated from papers. From previous, v3.0 release: 2,351 sets remain unchanged, 12 sets were renamed, and 29 became deprecated (9 by size filters, 7 by high similarity filter, and 13 for other reasons during review process.</p>
 
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  <li><strong>CP</strong>: canonical pathways <strong>(+572)</strong></li>
 
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    <ul>
 
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        <li><strong>Reactome</strong>
 
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<p>All sets were updated from v44 Reactome provided to MSigDB as part of our collaboration. [http://www.reactome.org/ Reactome] is a curated knowledgebase of biological pathways in humans. This update created 399 new sets, leaving 275 sets from v3.0 MSigDB unchanged and 155 deprecated. No sets were renamed.</p>
 
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        </li>
 
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        <li><strong>MIPS: </strong>Munich information center for protein sequences
 
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<p>The [http://mips.helmholtz-muenchen.de/genre/proj/corum CORUM] database provides a resource of manually annotated protein complexes from mammalian organisms. The MIPS gene sets correspond to human protein complexes extracted from the CORUM database (Released on February 17, 2012). All 132 sets are new.</p>
 
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        </li>
 
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        <li><strong>PID: </strong>Pathway Interaction Database
 
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<p>[http://pid.nci.nih.gov/ The Pathway Interaction Database (PID)] is a highly-structured, curated collection of information about known biomolecular interactions and key cellular processes assembled into signaling pathways. This was a collaborative project between the NCI and Nature Publishing Group (NPG) from 2006 until September 22nd, 2012, and is no longer being updated. As part of MSigDB collaboration with the PID resource, we extracted 196 gene sets extracted from the PID data (<tt>uniprot.tab</tt> file downloaded on May 15, 2012.</p>
 
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          </li>
 
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    </ul>
 
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</ul>
 
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<p>Renamed and deprecated sets are listed [[Mapping_between_v3.1_and_v3.0_gene_sets|here]].</p>
 
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<h2>Minor updates to the C4 collection</h2>
 
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<ul>
 
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<li><strong>CM: </strong>cancer modules (<strong>-23 gene sets</strong>).
 
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<p>Gene sets are <em>identical </em>to the modules described in [http://www.ncbi.nlm.nih.gov/pubmed/15448693 Segal et al., 2004]. The sets represent clusters of transcriptionally co-regulated genes that both share a common functional annotation and have been found significantly deregulated in tumors. Starting with a list of 2,849 gene sets from a variety of resources such as Gene Ontology, KEGG and others, the authors extracted 456 statistically significant regulatory modules from a large compendium of published microarray data spanning 22 tumor types.</p>
 
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<p>Original members of these sets were reverted to human Entrez Gene IDs as they appeared in original source files prior to v2.5 and the corresponding human gene symbols were derived thereafter. Twenty three sets were deprecated because they contained fewer than 10 human Entrez Gene IDs. Names of all sets were changed to upper case font to match the naming convention throughout MSigDB. Renamed and deprecated sets are listed [[Mapping_between_v3.1_and_v3.0_gene_sets|here]].</p>
 
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<p>For further details, refer to [http://www.broad.mit.edu/gsea/msigdb/collections.jsp MSigDB Collections].</p>
 
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</ul>
 
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<h3>For more information</h3>
 
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For complete descriptions of all collections or to download the updated  gene sets, go to the [http://www.broad.mit.edu/gsea/msigdb/collections.jsp Browse  Collections] page.
 
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<h2>Improved mapping to common gene identifiers </h2>
 
<h2>Improved mapping to common gene identifiers </h2>
  
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<p> MSigDB now uses <strong> Entrez Gene IDs </strong> as the <strong>common gene identifier </strong>for all gene sets. Gene sets come from a number of different sources and are originally specified using a variety of gene identifier. The MSigDB gene sets are converted to a common set of gene identifiers so they can be used in GSEA analyses, and other tools. Previous releases of MSigDB used human gene symbols for this purpose. Researchers prefer working with gene symbols because they can easily recognize, remember and put them in the context of their work. Unfortunately, a gene usually has multiple different symbols. Conversely, the same symbol may refer to a number of different genes. Finally, gene symbols change frequently. To overcome these issues, we now use Entrez Gene IDs as the universal gene identifier for all gene sets. Entrez Gene IDs uniquely identify human genes and never change. For convenience, we continue to display gene sets as human gene symbols by default. However, the symbols are now unambiguously derived from the corresponding human Entrez Gene IDs. For non-human original members, we first convert them to the organism-specific Entrez Gene IDs and then seek their orthologous counterparts as human Entrez Gene IDs. </p>
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<p> MSigDB now uses <strong> human Entrez Gene IDs </strong> as the <strong>common gene identifiers </strong>for all gene sets. Gene sets come from a number of different sources and are originally specified using a variety of gene identifiers. The MSigDB gene sets are converted to a common set of gene identifiers so they can be used in GSEA and other tools. Previous releases of MSigDB used human gene symbols for this purpose. Researchers prefer working with gene symbols because they can easily recognize, remember and put them in the context of their work. Unfortunately, a gene usually has multiple different symbols. Conversely, the same symbol may refer to a number of different genes. Finally, gene symbols change frequently. To overcome these issues, we now use Entrez Gene IDs as the universal gene identifier for all MSigDB gene sets. Entrez Gene IDs identify genes uniquely and never change. For convenience, we continue to display gene sets as human gene symbols by default. However, the symbols are now unambiguously derived from the corresponding human Entrez Gene IDs. For non-human original members, we first convert them to the organism-specific Entrez Gene IDs and then seek their orthologous counterparts as human Entrez Gene IDs. Finally, we derive human gene symbols from the corresponding common gene identifiers for all standard uses. Note that all gene sets are also available as the original identifiers specified by the source and as Entrez Gene IDs.</p>
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<p>We updated the gene symbols for all gene sets based on <tt>gene_info.gz</tt> and <tt>gene_history.gz</tt>, downloaded from the [http://www.ncbi.nlm.nih.gov/gene Entrez Gene] FTP site on November, 15, 2011.</p>
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<p>Human Entrez Gene IDs and the corresponding symbols for the MSigDB v3.1 gene sets are based on <tt>gene_info.gz</tt> and <tt>gene_history.gz</tt>, downloaded from the [http://www.ncbi.nlm.nih.gov/gene Entrez Gene] FTP site on November, 15, 2011. Mouse -> Human and Rat -> Human 1:1 orthologous relationships are from [http://www.informatics.jax.org/ Mouse Genome Informatics (MGI)].</p>
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MSigDB gene sets are subject to <strong>size and similarity restrictions</strong>.
 
MSigDB gene sets are subject to <strong>size and similarity restrictions</strong>.
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After mapping to human Entrez Gene IDs, the following filters were applied to exclude sets with
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After mapping to human Entrez Gene IDs, filters were applied to exclude sets with:
 
<ul>- fewer than 5 genes (C2:CGP only)</ul>
 
<ul>- fewer than 5 genes (C2:CGP only)</ul>
 
<ul>- fewer than 10 (all other collections)</ul>
 
<ul>- fewer than 10 (all other collections)</ul>
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<ul>- 90% or higher similarity (overlap) to other set(s) within a collection</ul>
 
<ul>- 90% or higher similarity (overlap) to other set(s) within a collection</ul>
  
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<h2>Other updates</h2>
+
<h2>New collection C6: Oncogenic Pathway Activation Modules</h2>
 +
 
 +
<p><strong> C6: Oncogenic Pathway Activation Modules</strong> is a <strong>new collection</strong> of 189 gene sets. These gene sets represent expression signatures derived directly from microarray data from experiments involving gain or loss of function of several established cancer genes in well defined, "clean" experimental systems. In this context, gain of function stands for increased activity of a cancer gene by means of over-expression or treatment with a chemical modulator. Conversely, loss of function stands for diminished activity of the cancer gene by means of RNAi knockdown, gene knockout, or enzymatic inhibition.</p>
 +
 
 +
<h2>New gene sets curated from papers </h2>
 +
<strong>1,035 new gene sets </strong>curated from papers were added to the <strong>C2:CGP</strong> (Chemical and Genetic Perturbations) sub-collection. In a review of the whole collection, 12 existing sets were renamed and 29 sets were deprecated. Renamed and deprecated sets are listed [[Mapping_between_v3.1_and_v3.0_gene_sets|here]].
  
 +
       
 +
<h2>New canonical pathway gene sets </h2>
 +
<p> The CP (Canonical Pathways) sub-collection has two new sources of gene sets. (1) <strong> 132 gene sets </strong> were collected from the Munich Information Center for Protein Sequences <strong>(MIPS)</strong>
 +
[http://mips.helmholtz-muenchen.de/genre/proj/corum CORUM] database, which provides a resource of manually annotated protein complexes from mammalian organisms. The gene sets correspond to human protein complexes extracted from the CORUM database released on February 17, 2012.
 +
(2) <strong> 196 gene sets </strong> were  collected from the
 +
[http://pid.nci.nih.gov/ Pathway Interaction Database] <strong>(PID)</strong>, which is a highly-structured, curated collection of information about known biomolecular interactions and key cellular processes assembled into signaling pathways. This was a collaborative project between the NCI and Nature Publishing Group (NPG) from 2006 until September 22nd, 2012, and is no longer being updated. In collaboration with the PID resource we extracted the gene sets from the PID data file (<tt>uniprot.tab</tt>) downloaded on May 15, 2012.
 +
          </p>
 +
<p>The sets in the CP (Canonical Pathways): the entire <strong> Reactome </strong> sub-collection was <strong>updated</strong> to version 44 of Reactome. [http://www.reactome.org/ Reactome] is a curated knowledgebase of biological pathways in humans. This update created 399 new sets, leaving 275 sets from v3.0 MSigDB unchanged and 155 deprecated. No sets were renamed. Deprecated sets are listed [[Mapping_between_v3.1_and_v3.0_gene_sets|here]].
 +
        </p>
  
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<p><Strong>Gene families:</strong>  
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<h2>Updates to C4: Cancer Modules</h2>
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Fixed a discrepancy between a family of transcription factors and homeodomain proteins. All homeodomain proteins are transcription factors. However, due to differences in sources and compilation procedures, some homeodomain proteins are not present among transcription factors. For this release, the transcription factors family now includes all genes annotated as homeodomain proteins.</p>
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<p>The gene sets in C4: Cancer Modules represent clusters of transcriptionally co-regulated genes that both share a common functional annotation and have been found significantly deregulated in tumors. They correspond to the modules described in [http://www.ncbi.nlm.nih.gov/pubmed/15448693 Segal et al., 2004].  
 +
For the MSigDB v3.1 release, these gene sets were re-mapped to gene symbols from the Entrez Gene IDs as they appeared in original source files prior to v2.5. 23 sets were deprecated because they contained fewer than 10 genes. Names of all other sets were changed to upper case font to match the naming convention throughout MSigDB. Renamed and deprecated sets are listed [[Mapping_between_v3.1_and_v3.0_gene_sets|here]].</p>
  
 +
<h2>Updates to gene families</h2>
 +
We fixed a discrepancy between the family of transcription factors and homeodomain proteins. All homeodomain proteins are transcription factors. However, due to differences in sources and compilation procedures, some homeodomain proteins were not present in the transcription factors gene family.  This has been fixed in the 3.1 release.
  
−
<p><Strong>Viewing previous versions of MSigDB:</strong>  
+
<h2>Viewing previous versions of MSigDB</h2>  
 
The MSigDB v3.0 and v2.5 files are archived and are available at [http://www.broadinstitute.org/gsea/downloads.jsp Downloads]  page. You can view them through the MSigDB Browser tool in the GSEA desktop application. Please see [[GSEA_v2.08._Release_Notes|GSEA 2.0.8 Release Notes]] for details.
 
The MSigDB v3.0 and v2.5 files are archived and are available at [http://www.broadinstitute.org/gsea/downloads.jsp Downloads]  page. You can view them through the MSigDB Browser tool in the GSEA desktop application. Please see [[GSEA_v2.08._Release_Notes|GSEA 2.0.8 Release Notes]] for details.

Latest revision as of 02:10, 25 September 2016

GSEA Home | Downloads | Molecular Signatures Database | Documentation | Contact

Improved mapping to common gene identifiers

MSigDB now uses human Entrez Gene IDs as the common gene identifiers for all gene sets. Gene sets come from a number of different sources and are originally specified using a variety of gene identifiers. The MSigDB gene sets are converted to a common set of gene identifiers so they can be used in GSEA and other tools. Previous releases of MSigDB used human gene symbols for this purpose. Researchers prefer working with gene symbols because they can easily recognize, remember and put them in the context of their work. Unfortunately, a gene usually has multiple different symbols. Conversely, the same symbol may refer to a number of different genes. Finally, gene symbols change frequently. To overcome these issues, we now use Entrez Gene IDs as the universal gene identifier for all MSigDB gene sets. Entrez Gene IDs identify genes uniquely and never change. For convenience, we continue to display gene sets as human gene symbols by default. However, the symbols are now unambiguously derived from the corresponding human Entrez Gene IDs. For non-human original members, we first convert them to the organism-specific Entrez Gene IDs and then seek their orthologous counterparts as human Entrez Gene IDs. Finally, we derive human gene symbols from the corresponding common gene identifiers for all standard uses. Note that all gene sets are also available as the original identifiers specified by the source and as Entrez Gene IDs.

Human Entrez Gene IDs and the corresponding symbols for the MSigDB v3.1 gene sets are based on gene_info.gz and gene_history.gz, downloaded from the Entrez Gene FTP site on November, 15, 2011. Mouse -> Human and Rat -> Human 1:1 orthologous relationships are from Mouse Genome Informatics (MGI).

MSigDB gene sets are subject to size and similarity restrictions. After mapping to human Entrez Gene IDs, filters were applied to exclude sets with:

    - fewer than 5 genes (C2:CGP only)
    - fewer than 10 (all other collections)
    - more than 2,000 genes
    - 90% or higher similarity (overlap) to other set(s) within a collection

New collection C6: Oncogenic Pathway Activation Modules

C6: Oncogenic Pathway Activation Modules is a new collection of 189 gene sets. These gene sets represent expression signatures derived directly from microarray data from experiments involving gain or loss of function of several established cancer genes in well defined, "clean" experimental systems. In this context, gain of function stands for increased activity of a cancer gene by means of over-expression or treatment with a chemical modulator. Conversely, loss of function stands for diminished activity of the cancer gene by means of RNAi knockdown, gene knockout, or enzymatic inhibition.

New gene sets curated from papers

1,035 new gene sets curated from papers were added to the C2:CGP (Chemical and Genetic Perturbations) sub-collection. In a review of the whole collection, 12 existing sets were renamed and 29 sets were deprecated. Renamed and deprecated sets are listed here.


New canonical pathway gene sets

The CP (Canonical Pathways) sub-collection has two new sources of gene sets. (1) 132 gene sets were collected from the Munich Information Center for Protein Sequences (MIPS) CORUM database, which provides a resource of manually annotated protein complexes from mammalian organisms. The gene sets correspond to human protein complexes extracted from the CORUM database released on February 17, 2012. (2) 196 gene sets were collected from the Pathway Interaction Database (PID), which is a highly-structured, curated collection of information about known biomolecular interactions and key cellular processes assembled into signaling pathways. This was a collaborative project between the NCI and Nature Publishing Group (NPG) from 2006 until September 22nd, 2012, and is no longer being updated. In collaboration with the PID resource we extracted the gene sets from the PID data file (uniprot.tab) downloaded on May 15, 2012.

The sets in the CP (Canonical Pathways): the entire Reactome sub-collection was updated to version 44 of Reactome. Reactome is a curated knowledgebase of biological pathways in humans. This update created 399 new sets, leaving 275 sets from v3.0 MSigDB unchanged and 155 deprecated. No sets were renamed. Deprecated sets are listed here.

Updates to C4: Cancer Modules

The gene sets in C4: Cancer Modules represent clusters of transcriptionally co-regulated genes that both share a common functional annotation and have been found significantly deregulated in tumors. They correspond to the modules described in Segal et al., 2004. For the MSigDB v3.1 release, these gene sets were re-mapped to gene symbols from the Entrez Gene IDs as they appeared in original source files prior to v2.5. 23 sets were deprecated because they contained fewer than 10 genes. Names of all other sets were changed to upper case font to match the naming convention throughout MSigDB. Renamed and deprecated sets are listed here.

Updates to gene families

We fixed a discrepancy between the family of transcription factors and homeodomain proteins. All homeodomain proteins are transcription factors. However, due to differences in sources and compilation procedures, some homeodomain proteins were not present in the transcription factors gene family. This has been fixed in the 3.1 release.

Viewing previous versions of MSigDB

The MSigDB v3.0 and v2.5 files are archived and are available at Downloads page. You can view them through the MSigDB Browser tool in the GSEA desktop application. Please see GSEA 2.0.8 Release Notes for details.

Retrieved from "https://software.broadinstitute.org/cancer/software/gsea/wiki/index.php?title=MSigDB_v3.1_Release_Notes&oldid=3996"