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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Predictive networks: a flexible, open source, web application for integration and analysis of human gene networks</title><author><name sortKey="Haibe Kains, Benjamin" sort="Haibe Kains, Benjamin" uniqKey="Haibe Kains B" first="Benjamin" last="Haibe-Kains">Benjamin Haibe-Kains</name><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute,</nlm:aff></affiliation><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics, Harvard School of Public Health, Boston, MA 02215, USA,</nlm:aff></affiliation></author><author><name sortKey="Olsen, Catharina" sort="Olsen, Catharina" uniqKey="Olsen C" first="Catharina" last="Olsen">Catharina Olsen</name><affiliation><nlm:aff id="gkr1050-AFF1">Machine Learning Group, Université Libre de Bruxelles, Brussels, Belgium,</nlm:aff></affiliation></author><author><name sortKey="Djebbari, Amira" sort="Djebbari, Amira" uniqKey="Djebbari A" first="Amira" last="Djebbari">Amira Djebbari</name><affiliation><nlm:aff id="gkr1050-AFF1">Ontario Cancer Institute, Princess Margaret Hospital/UHN, and the Campbell Family Institute for Cancer Research, University of Toronto, Toronto, ON M5G 1L7, Canada,</nlm:aff></affiliation></author><author><name sortKey="Bontempi, Gianluca" sort="Bontempi, Gianluca" uniqKey="Bontempi G" first="Gianluca" last="Bontempi">Gianluca Bontempi</name><affiliation><nlm:aff id="gkr1050-AFF1">Machine Learning Group, Université Libre de Bruxelles, Brussels, Belgium,</nlm:aff></affiliation></author><author><name sortKey="Correll, Mick" sort="Correll, Mick" uniqKey="Correll M" first="Mick" last="Correll">Mick Correll</name><affiliation><nlm:aff wicri:cut=" and" id="gkr1050-AFF1">Center for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215</nlm:aff></affiliation></author><author><name sortKey="Bouton, Christopher" sort="Bouton, Christopher" uniqKey="Bouton C" first="Christopher" last="Bouton">Christopher Bouton</name><affiliation><nlm:aff id="gkr1050-AFF1">Entagen, Newburyport, MA 01950, USA</nlm:aff></affiliation></author><author><name sortKey="Quackenbush, John" sort="Quackenbush, John" uniqKey="Quackenbush J" first="John" last="Quackenbush">John Quackenbush</name><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute,</nlm:aff></affiliation><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics, Harvard School of Public Health, Boston, MA 02215, USA,</nlm:aff></affiliation><affiliation><nlm:aff wicri:cut=" and" id="gkr1050-AFF1">Center for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">22096235</idno><idno type="pmc">3245161</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245161</idno><idno type="RBID">PMC:3245161</idno><idno type="doi">10.1093/nar/gkr1050</idno><date when="2011">2011</date><idno type="wicri:Area/Pmc/Corpus">000404</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Predictive networks: a flexible, open source, web application for integration and analysis of human gene networks</title><author><name sortKey="Haibe Kains, Benjamin" sort="Haibe Kains, Benjamin" uniqKey="Haibe Kains B" first="Benjamin" last="Haibe-Kains">Benjamin Haibe-Kains</name><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute,</nlm:aff></affiliation><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics, Harvard School of Public Health, Boston, MA 02215, USA,</nlm:aff></affiliation></author><author><name sortKey="Olsen, Catharina" sort="Olsen, Catharina" uniqKey="Olsen C" first="Catharina" last="Olsen">Catharina Olsen</name><affiliation><nlm:aff id="gkr1050-AFF1">Machine Learning Group, Université Libre de Bruxelles, Brussels, Belgium,</nlm:aff></affiliation></author><author><name sortKey="Djebbari, Amira" sort="Djebbari, Amira" uniqKey="Djebbari A" first="Amira" last="Djebbari">Amira Djebbari</name><affiliation><nlm:aff id="gkr1050-AFF1">Ontario Cancer Institute, Princess Margaret Hospital/UHN, and the Campbell Family Institute for Cancer Research, University of Toronto, Toronto, ON M5G 1L7, Canada,</nlm:aff></affiliation></author><author><name sortKey="Bontempi, Gianluca" sort="Bontempi, Gianluca" uniqKey="Bontempi G" first="Gianluca" last="Bontempi">Gianluca Bontempi</name><affiliation><nlm:aff id="gkr1050-AFF1">Machine Learning Group, Université Libre de Bruxelles, Brussels, Belgium,</nlm:aff></affiliation></author><author><name sortKey="Correll, Mick" sort="Correll, Mick" uniqKey="Correll M" first="Mick" last="Correll">Mick Correll</name><affiliation><nlm:aff wicri:cut=" and" id="gkr1050-AFF1">Center for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215</nlm:aff></affiliation></author><author><name sortKey="Bouton, Christopher" sort="Bouton, Christopher" uniqKey="Bouton C" first="Christopher" last="Bouton">Christopher Bouton</name><affiliation><nlm:aff id="gkr1050-AFF1">Entagen, Newburyport, MA 01950, USA</nlm:aff></affiliation></author><author><name sortKey="Quackenbush, John" sort="Quackenbush, John" uniqKey="Quackenbush J" first="John" last="Quackenbush">John Quackenbush</name><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute,</nlm:aff></affiliation><affiliation><nlm:aff id="gkr1050-AFF1">Department of Biostatistics, Harvard School of Public Health, Boston, MA 02215, USA,</nlm:aff></affiliation><affiliation><nlm:aff wicri:cut=" and" id="gkr1050-AFF1">Center for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215</nlm:aff></affiliation></author></analytic><series><title level="j">Nucleic Acids Research</title><idno type="ISSN">0305-1048</idno><idno type="eISSN">1362-4962</idno><imprint><date when="2011">2011</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Genomics provided us with an unprecedented quantity of data on the genes that are activated or repressed in a wide range of phenotypes. We have increasingly come to recognize that defining the networks and pathways underlying these phenotypes requires both the integration of multiple data types and the development of advanced computational methods to infer relationships between the genes and to estimate the predictive power of the networks through which they interact. To address these issues we have developed <italic>Predictive Networks</italic> (PN), a flexible, open-source, web-based application and data services framework that enables the integration, navigation, visualization and analysis of gene interaction networks. The primary goal of PN is to allow biomedical researchers to evaluate experimentally derived gene lists in the context of large-scale gene interaction networks. The PN analytical pipeline involves two key steps. The first is the collection of a comprehensive set of known gene interactions derived from a variety of publicly available sources. The second is to use these ‘known’ interactions together with gene expression data to infer robust gene networks. The PN web application is accessible from <ext-link ext-link-type="uri" xlink:href="http://predictivenetworks.org">http://predictivenetworks.org</ext-link>. The PN code base is freely available at <ext-link ext-link-type="uri" xlink:href="https://sourceforge.net/projects/predictivenets/">https://sourceforge.net/projects/predictivenets/</ext-link>.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Spellman, Pt" uniqKey="Spellman P">PT Spellman</name></author><author><name sortKey="Sherlock, G" uniqKey="Sherlock G">G Sherlock</name></author><author><name sortKey="Zhang, Mq" uniqKey="Zhang M">MQ Zhang</name></author><author><name sortKey="Iyer, Vr" uniqKey="Iyer V">VR Iyer</name></author><author><name sortKey="Anders, K" uniqKey="Anders K">K Anders</name></author><author><name sortKey="Eisen, Mb" uniqKey="Eisen M">MB Eisen</name></author><author><name sortKey="Brown, Po" uniqKey="Brown P">PO Brown</name></author><author><name sortKey="Botstein, D" uniqKey="Botstein D">D Botstein</name></author><author><name sortKey="Futcher, B" uniqKey="Futcher B">B 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Nucleic Acids Res</journal-id><journal-id journal-id-type="iso-abbrev">Nucleic Acids Res</journal-id><journal-id journal-id-type="publisher-id">nar</journal-id><journal-id journal-id-type="hwp">nar</journal-id><journal-title-group><journal-title>Nucleic Acids Research</journal-title></journal-title-group><issn pub-type="ppub">0305-1048</issn><issn pub-type="epub">1362-4962</issn><publisher><publisher-name>Oxford University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">22096235</article-id><article-id pub-id-type="pmc">3245161</article-id><article-id pub-id-type="doi">10.1093/nar/gkr1050</article-id><article-id pub-id-type="publisher-id">gkr1050</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group></article-categories><title-group><article-title>Predictive networks: a flexible, open source, web application for integration and analysis of human gene networks</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Haibe-Kains</surname><given-names>Benjamin</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>1</sup></xref><xref ref-type="aff" rid="gkr1050-AFF1"><sup>2</sup></xref><xref ref-type="corresp" rid="gkr1050-COR1">*</xref></contrib><contrib contrib-type="author"><name><surname>Olsen</surname><given-names>Catharina</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>3</sup></xref></contrib><contrib contrib-type="author"><name><surname>Djebbari</surname><given-names>Amira</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>4</sup></xref></contrib><contrib contrib-type="author"><name><surname>Bontempi</surname><given-names>Gianluca</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>3</sup></xref></contrib><contrib contrib-type="author"><name><surname>Correll</surname><given-names>Mick</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>5</sup></xref></contrib><contrib contrib-type="author"><name><surname>Bouton</surname><given-names>Christopher</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>6</sup></xref></contrib><contrib contrib-type="author"><name><surname>Quackenbush</surname><given-names>John</given-names></name><xref ref-type="aff" rid="gkr1050-AFF1"><sup>1</sup></xref><xref ref-type="aff" rid="gkr1050-AFF1"><sup>2</sup></xref><xref ref-type="aff" rid="gkr1050-AFF1"><sup>5</sup></xref><xref ref-type="corresp" rid="gkr1050-COR1">*</xref></contrib></contrib-group><aff id="gkr1050-AFF1"><sup>1</sup>Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute,<sup>2</sup>Department of Biostatistics, Harvard School of Public Health, Boston, MA 02215, USA,<sup>3</sup>Machine Learning Group, Université Libre de Bruxelles, Brussels, Belgium,<sup>4</sup>Ontario Cancer Institute, Princess Margaret Hospital/UHN, and the Campbell Family Institute for Cancer Research, University of Toronto, Toronto, ON M5G 1L7, Canada,<sup>5</sup>Center for Cancer Computational Biology, Dana-Farber Cancer Institute, Boston, MA 02215 and<sup>6</sup>Entagen, Newburyport, MA 01950, USA</aff><author-notes><corresp id="gkr1050-COR1">*To whom correspondence should be addressed. Email: <email>bhaibeka@jimmy.harvard.edu</email></corresp><corresp>Correspondence may also be addressed to John Quackenbush. Tel: <phone>+ 1 617 632 3012</phone>; Fax: <fax>+1 617 632 2444</fax>; Email: <email>johnq@jimmy.harvard.edu</email></corresp></author-notes><pub-date pub-type="ppub"><month>1</month><year>2012</year></pub-date><pub-date pub-type="epub"><day>16</day><month>11</month><year>2011</year></pub-date><pub-date pub-type="pmc-release"><day>16</day><month>11</month><year>2011</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on the
<volume>40</volume><issue>Database issue</issue><issue-title>Database issue</issue-title><fpage>D866</fpage><lpage>D875</lpage><history><date date-type="received"><day>15</day><month>8</month><year>2011</year></date><date date-type="rev-recd"><day>9</day><month>10</month><year>2011</year></date><date date-type="accepted"><day>23</day><month>10</month><year>2011</year></date></history><permissions><copyright-statement>© The Author(s) 2011. Published by Oxford University Press.</copyright-statement><copyright-year>2011</copyright-year><license license-type="creative-commons" xlink:href="http://creativecommons.org/licenses/by-nc/3.0"><license-p><pmc-comment>CREATIVE COMMONS</pmc-comment>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/3.0">http://creativecommons.org/licenses/by-nc/3.0</ext-link>), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><abstract><p>Genomics provided us with an unprecedented quantity of data on the genes that are activated or repressed in a wide range of phenotypes. We have increasingly come to recognize that defining the networks and pathways underlying these phenotypes requires both the integration of multiple data types and the development of advanced computational methods to infer relationships between the genes and to estimate the predictive power of the networks through which they interact. To address these issues we have developed <italic>Predictive Networks</italic> (PN), a flexible, open-source, web-based application and data services framework that enables the integration, navigation, visualization and analysis of gene interaction networks. The primary goal of PN is to allow biomedical researchers to evaluate experimentally derived gene lists in the context of large-scale gene interaction networks. The PN analytical pipeline involves two key steps. The first is the collection of a comprehensive set of known gene interactions derived from a variety of publicly available sources. The second is to use these ‘known’ interactions together with gene expression data to infer robust gene networks. The PN web application is accessible from <ext-link ext-link-type="uri" xlink:href="http://predictivenetworks.org">http://predictivenetworks.org</ext-link>. The PN code base is freely available at <ext-link ext-link-type="uri" xlink:href="https://sourceforge.net/projects/predictivenets/">https://sourceforge.net/projects/predictivenets/</ext-link>.</p></abstract><counts><page-count count="10"></page-count></counts></article-meta></front><body><sec sec-type="intro"><title>INTRODUCTION</title><p>The sequencing of the human genome and the development of new approaches including genomics (DNA), transcriptomics (RNA), methylomics (epigenetic methylation) and proteomics (protein), have given scientists the tools necessary to amass comprehensive datasets of genomic profiles in a range of cellular and organismal phenotypes and in response to a variety of perturbations. While the hope was that we could use these data to understand the link between genotype and phenotype, we have increasingly come to recognize that the cellular regulatory processes are more complex than we had once imagined. We now understand that it is generally not individual genes, but networks of interacting genes and gene products, which collectively interact to define phenotypes and the alterations that occur in the development of disease.</p><p>Network models were first applied to gene expression data from a yeast cell cycle experiment in which synchronized cells were profiled over a carefully planned time-course (<xref rid="gkr1050-B1" ref-type="bibr">1</xref>). Friedman <italic>et al.</italic> (<xref rid="gkr1050-B2" ref-type="bibr">2</xref>) analyzed these data in a Bayesian Network framework to develop a predictive cell-cycle model. Since this early work, there have been many other methods developed to model networks while addressing the intrinsic complexity of high-throughput genomic data (high feature-to-sample ratio, high-level of noise and co-linearity) (<xref rid="gkr1050-B1" ref-type="bibr">1–9</xref>). Other web-based tools, such as ASIAN (<xref rid="gkr1050-B10" ref-type="bibr">10</xref>), SEBINI (<xref rid="gkr1050-B11" ref-type="bibr">11</xref>) and CARRIE (<xref rid="gkr1050-B12" ref-type="bibr">12</xref>), attempt to infer interaction networks based solely on genomic data. However, few methods have come into widespread use and often fail to produce useful network models (<xref rid="gkr1050-B13" ref-type="bibr">13</xref>,<xref rid="gkr1050-B14" ref-type="bibr">14</xref>). The problem may be that most methods deal solely with genomic data and ignore what may be the best resource we have to efficiently constraint the fitting of network models: the collection of existing prior knowledge captured in published biomedical literature and structured databases.</p><p>There are a number of web-based tools have been developed to retrieve putative gene–gene interactions based on descriptions in PubMed abstracts and in biological databases, including GeneMANIA (<xref rid="gkr1050-B15" ref-type="bibr">15</xref>) and iHOP/GIM (<xref rid="gkr1050-B16" ref-type="bibr">16</xref>,<xref rid="gkr1050-B17" ref-type="bibr">17</xref>). Commercial tools, such as GeneGO (<xref rid="gkr1050-B18" ref-type="bibr">18</xref>) and Ingenuity Pathway Analysis (<xref rid="gkr1050-B19" ref-type="bibr">19</xref>), combine this functionality with enrichment analysis that allows users to estimate significance of key biological functions and processes represented among a list of genes. But these tools generally treat the networks inferred from prior knowledge as scaffolds onto which gene expression data is projected, rather than as a tool to help guide network inference using genomic data. And further, we must recognize that a ‘known network’ based on published information may not represent the true biological network or may fail to capture the network alterations that may be associated with the phenotypes or conditions being analyzed in a particular study.</p><p>Here we present <italic>Predictive Networks</italic> (PN; <ext-link ext-link-type="uri" xlink:href="http://predictivenetworks.org">http://predictivenetworks.org</ext-link>), a flexible, open-source, web-based application and data services framework for inferring networks using gene expression data in combination with gene–gene interactions mined from the full-text biomedical literature and publicly available network and pathway databases. PN allows users to create ‘phenomenological’ models based on the observed data that facilitate hypothesis generation and that can help identify the most relevant genes for distinguishing between phenotypes in an analysis.</p></sec><sec><title>COLLECTING, INTEGRATING AND ANALYZING GENE INTERACTIONS</title><p>Gene–gene interactions are described through the action of one gene on another. For example, we can define an interaction through the sentence ‘PGC is inhibited by SIRT1’ or ‘CCNT1 regulates PGC’ which have the basic English language structure:
<disp-quote><p>[<italic>Subject</italic>; <italic>Predicate</italic>; <italic>Object</italic>].</p></disp-quote>This structure, called a ‘triple’, is the basis of data representation in Semantic Web technologies (<xref rid="gkr1050-B20" ref-type="bibr">20</xref>) and as such they provide a natural way of describing and characterizing interactions and networks. For example, if we know that PGC is inhibited by SIRT1 and that CCNT1 regulates PGC then we have a simple network suggesting both SIRT1 and CCNT1 influence PGC (<xref ref-type="fig" rid="gkr1050-F1">Figure 1</xref>A); this network is actually composed of the two triples [‘PGC’, ‘is inhibited by’, ‘SIRT1’] and [‘CCNT1’, ‘regulates’, ‘PGC’] extracted from a PubMed abstract or a full-text article (<xref ref-type="fig" rid="gkr1050-F1">Figure 1</xref>B). Because there are now a large number of tools for storing, searching and manipulating triples, we chose to use triples as the basic representation of gene–gene interactions in PN.
<fig id="gkr1050-F1" position="float"><label>Figure 1.</label><caption><p>Overview of the core PN concepts ultimately representing a gene interaction network. A gene interaction network (<bold>A</bold>) is a collection of triples (<bold>B</bold>) where each triple involves two genes (for example PGC, SIRT1) and a predicate (for example ‘is inhibited by’); each gene is described by a number of meta-data, incuding annotations; each gene can be part of a users’ gene list.</p></caption><graphic xlink:href="gkr1050f1"></graphic></fig></p><p>In representing interactions, the Subject and Object are both genes. One of the challenges we faced in creating a store of interactions was the frequent use of synonyms and ‘common names’ for genes rather than the standard Gene Symbols. The Predicates capture the interactions between genes and include terms like ‘regulates’ or ‘is inhibited by’ that capture directional interactions (<italic>Subject</italic> → O<italic>bject</italic> or <italic>Subject</italic> ← <italic>Object</italic>, respectively).</p><p>One subtle challenge in capturing and representing triples is negation, and for our triples we include a flag representing the evidence in a sentence supporting the presence or absence of an interaction, as inferred from the predicate. For example, we want to distinguish between the positive interaction, ‘regulates’, and the negative interaction ‘does not regulate’. We also recognize that the literature often contains contradictory evidence for the direction of the interaction between two genes; one way to decide likely directionality in an interaction is to weight interactions based on the number of times they have been described in various publications.</p><p>To create the database underlying the PN web application, we used two main sources from which we extracted triples (<xref ref-type="table" rid="gkr1050-T1">Table 1</xref>): the published biomedical literature including both abstracts catalogued in PubMed and full-text articles available through PubMed Central, and structured biological databases including Pathway Commons (<xref rid="gkr1050-B21" ref-type="bibr">21</xref>) and functional interactions identified in the recent publication of Stein <italic>et al</italic>. (<xref rid="gkr1050-B22" ref-type="bibr">22</xref>). The method we used to extract triples depends on the data source. Extraction of triples from structured pathway databases requires minimal processing and conversion to capture the interactions. However, deducing triples and their context from the biomedical literature is a challenging task that required we develop a text mining pipeline (<xref ref-type="fig" rid="gkr1050-F2">Figure 2</xref>) that combined custom parsing and text mining systems (available through sourceforge, <ext-link ext-link-type="uri" xlink:href="https://sourceforge.net/projects/predictivenets">https://sourceforge.net/projects/predictivenets</ext-link>) together with the LingPipe text processing library (<xref rid="gkr1050-B23" ref-type="bibr">23</xref>).
<fig id="gkr1050-F2" position="float"><label>Figure 2.</label><caption><p>Text mining pipeline. PubMed abstracts and full-text articles from PubMed Central are extracted and formatted so they can be analyzed using the common text interface. The processed text is then mined using a combination of custom parsing scripts and the LingPipe text processing library to identify gene interaction triples and their contexts. These triples are then used to infer gene interactions networks used throughout PN.</p></caption><graphic xlink:href="gkr1050f2"></graphic></fig><table-wrap id="gkr1050-T1" position="float"><label>Table 1.</label><caption><p>Description of data sources</p></caption><table frame="hsides" rules="groups"><thead align="left"><tr><th rowspan="1" colspan="1"></th><th colspan="2" align="center" rowspan="1">Biomedical literature<hr></hr></th><th colspan="2" align="center" rowspan="1">Structured biological databases<hr></hr></th></tr><tr><th rowspan="1" colspan="1"></th><th rowspan="1" colspan="1">PubMed abstracts</th><th rowspan="1" colspan="1">PubMed Central full-text articles</th><th rowspan="1" colspan="1">Function interaction</th><th rowspan="1" colspan="1">Pathways common</th></tr></thead><tbody align="left"><tr><td rowspan="1" colspan="1">No. of genes</td><td rowspan="1" colspan="1">11 443</td><td rowspan="1" colspan="1">7128</td><td rowspan="1" colspan="1">9408</td><td rowspan="1" colspan="1">11 535</td></tr><tr><td rowspan="1" colspan="1">No. of interactions</td><td rowspan="1" colspan="1">59 159</td><td rowspan="1" colspan="1">21 863</td><td rowspan="1" colspan="1">1 81 013</td><td rowspan="1" colspan="1">1 142 763</td></tr><tr><td rowspan="1" colspan="1">No. of contexts</td><td rowspan="1" colspan="1">102 987</td><td rowspan="1" colspan="1">84 507</td><td rowspan="1" colspan="1">N/A</td><td rowspan="1" colspan="1">N/A</td></tr><tr><td rowspan="1" colspan="1">Average no. of contexts per article</td><td rowspan="1" colspan="1">1.78</td><td rowspan="1" colspan="1">7.34</td><td rowspan="1" colspan="1">N/A</td><td rowspan="1" colspan="1">N/A</td></tr><tr><td rowspan="1" colspan="1">Average no. of contexts per sentence</td><td rowspan="1" colspan="1">1.53</td><td rowspan="1" colspan="1">3.59</td><td rowspan="1" colspan="1">N/A</td><td rowspan="1" colspan="1">N/A</td></tr><tr><td rowspan="1" colspan="1">Source</td><td rowspan="1" colspan="1">pubmed.org</td><td rowspan="1" colspan="1">pubmed.org</td><td rowspan="1" colspan="1">string-db.org</td><td rowspan="1" colspan="1">Pathwaycommons.org</td></tr></tbody></table><table-wrap-foot><fn id="gkr1050-TF1"><p>The data sources used in PN including the number of genes identified, the interactions found, number of contexts, average number of such contexts per article and per sentence, and the URL from which the primary data were downloaded. No contexts have been extracted from the structured biological databases (NA, not applicable).</p></fn></table-wrap-foot></table-wrap></p><p>The text mining pipeline starts by extracting complete text from the PubMed Open Access/Abstracts text XML files, which are available in compressed form at <ext-link ext-link-type="uri" xlink:href="ftp.ncbi.nlm.nih.gov/pub/pmc/articles">ftp.ncbi.nlm.nih.gov/pub/pmc/articles</ext-link>.*.tar.gz. A predicate ontology is used to detect predicates in each sentence from each article. A gene name detection approach is then used to identify genes appearing on either side of the predicate. If a gene–gene interaction triple is identified a final scan is performed upon the text to detect context.</p><p>To derive contexts for gene interaction triples, we used terms and phrases used in MeSH (<xref rid="gkr1050-B24" ref-type="bibr">24</xref>) and the Gene Ontology project (<xref rid="gkr1050-B25" ref-type="bibr">25</xref>) to provide an ontological representation of context keywords. We assume that the source from which triples are being extracted provides an overarching context for those gene interactions. Given this assumption we pull contextual keywords from the entire body of each source and apply those contexts to each interaction derived from the source. In assessing the relative value of derivation of triples from full-text sources versus abstracts alone, we observed that the number of contexts per triples extracted from full-text articles is significantly larger than from abstracts (Fisher’s exact test <italic>P</italic> < 0.001; <xref ref-type="table" rid="gkr1050-T1">Table 1</xref>).</p><sec sec-type="cases"><title>Use Case 1: gene-centered network searches</title><p>One of the primary questions that users of a resource such as this want to ask is ‘What other genes interact with my gene of interest?’ This is a relatively easy question to answer through the PN web application as all interactions are stored as triples and a network can be represented as a collection of triples connected either through common Subjects or Objects (<xref ref-type="fig" rid="gkr1050-F1">Figure 1</xref>A and B).</p><p>The PN web application allows users to enter single gene names and to find genes that connect to it, and then genes that connect to its connection partners up to whatever distance one might desire. The PN web application allows users to submit single gene names as queries. These are disambiguated and mapped to standard identifiers which are then queried against the collected PN triples. The resulting network built from interactions represented in the triples is then visualized as a graph that can then be filtered based on the following criteria:
<list list-type="bullet"><list-item><p>Context: Networks can be limited to interactions reported in a specific context. For example a network centered on gene ‘RB1’ could be built using only triples identified in the context of ‘tumor suppressor’.</p></list-item><list-item><p>Number of occurrences: Networks can be built only using interactions that are supported by a sufficient number of triples. For example, users can specify that only interactions reported more than five times should be used to build the network.</p></list-item><list-item><p>Connectivity: The default network that is presented only contains the gene and its primary (first degree) connections. Users can increase the connectivity to display more distant inferred connections to their target gene of interest and</p></list-item><list-item><p>Max Genes: Networks can be limited to display a maximum number of genes; genes involved in the interaction supported by the largest number of triples will be selected. The default maximum of genes is 20.</p></list-item></list>In the network display, users can click on a gene name to highlight that gene and its connections. Clicking on a gene node in the network expands the network to include neighbors of that gene. Networks can be exported as a table (comma-separated value or tab-delimited spreadsheets), an image or a GML file [Graph Modeling Language (<xref rid="gkr1050-B26" ref-type="bibr">26</xref>)] which can be imported into Cytoscape (<xref rid="gkr1050-B27" ref-type="bibr">27</xref>,<xref rid="gkr1050-B28" ref-type="bibr">28</xref>) or NAVIGaTOR (<xref rid="gkr1050-B29" ref-type="bibr">29</xref>) to allow further network exploration.</p></sec><sec sec-type="cases"><title>Use Case 2: identifying connections in gene lists</title><p>Most genomic analyses compare two or more phenotypic conditions and report a list of genes that are significant for distinguishing between experimental groups, but the connections between the genes in the ‘gene list’ are often unknown. The PN web application allows users to upload a gene list and, based on user-defined parameters, searches for reported interactions stored as triples that link the genes in the list. The resulting gene interaction network is displayed in a graphical format with similar features to that described for single genes and can be exported in a variety of formats for presentation or further exploration.</p></sec><sec sec-type="cases"><title>Use Case 3: network inference from literature-inferred interactions and genomic data</title><p>Inferring networks from genomic data is a challenging problem. Learning the network architecture without some prior constraints requires consideration of all possible pairwise connections between genes, a problem that has been shown to be NP-hard (<xref rid="gkr1050-B30" ref-type="bibr">30</xref>). Indeed, for directed networks, the number of possible graphs is super-exponential in the number of nodes; for eight genes, there are 7.8 × 10<sup>11</sup> network configurations that must be considered to completely explore the problem’s ‘state space’. Consequently, most approaches are prone to overfitting and fail to find ‘realistic’ networks.</p><p>Our primary goal in developing the PN application was to analyze genomic data using literature inferred relationships to help build predictive network models. Consequently, the PN application allows users to provide their own gene expression data and to use one of two methods to deduce network interactions. We previously described a seeded Bayesian network approach and demonstrated that the use of prior information could significantly improve the quality of the inferred network models (<xref rid="gkr1050-B9" ref-type="bibr">9</xref>). But inferring Bayesian networks for large numbers of genes, even with a seeded prior remains computationally challenging. Regression-based methods are not able to represent the full joint distribution of the data as Bayesian networks do, but they have been shown to have promising performance and to enable inference of extremely large biological networks (<xref rid="gkr1050-B31" ref-type="bibr">31</xref>). To partially address the problem of network inference, the PN web application includes the seeded Bayesian network inference we had described previously (<xref rid="gkr1050-B9" ref-type="bibr">9</xref>) and a novel regression-based technique (<xref rid="gkr1050-B32" ref-type="bibr">32</xref>).</p><p>Both Bayesian and regression network inference starts with a normalized gene expression dataset and a ‘Gene List’ selected by users based on their own criteria. The gene expression data might be generated with any microarray platform and normalization techniques, although the use of Affymetrix (<ext-link ext-link-type="uri" xlink:href="http://www.affymetrix.com">http://www.affymetrix.com</ext-link>) data normalized by (f)RMA (<xref rid="gkr1050-B33" ref-type="bibr">33</xref>,<xref rid="gkr1050-B34" ref-type="bibr">34</xref>) is a good choice given that they are widely used. The gene list might be a set of genes determined to be statistically significant for distinguishing sample groups or the genes in a pathway they would like to explore in the context of their expression data. Both methods use the gene list to deduce an initial network based solely on the PN triples as a starting point (or set of ‘priors’) that can evolve based on relationships represented in the users’ gene expression data, allowing new interactions between genes to be identified or poorly supported interactions to be eliminated. Minimum and maximum size for gene expression datasets and gene lists are further described in the <ext-link ext-link-type="uri" xlink:href="http://nar.oxfordjournals.org/cgi/content/full/gkr1050/DC1">Supplementary Data section</ext-link>.</p><p>For both methods, users upload their gene expression data and gene lists, and provide a name for their analysis. The regression-based method is run by default, but users can select ‘Advanced Options’ to select a specific method and to set parameters for the analysis; a detailed description of the parameters is provided in the <ext-link ext-link-type="uri" xlink:href="http://nar.oxfordjournals.org/cgi/content/full/gkr1050/DC1">Supplementary Data section</ext-link>. The inferred interactions are visualized and the networks and associated data can be downloaded for further analysis.</p><p>Because the quality of inference is not uniform over the network, we developed both interaction-specific and gene-specific statistical measures to assess the quality of the constituent subnetworks that comprise the full network, This allows users to focus on the subnetworks, interactions and genes that are well supported by the data. A description of these statistics is provided in the <ext-link ext-link-type="uri" xlink:href="http://nar.oxfordjournals.org/cgi/content/full/gkr1050/DC1">Supplementary Data section</ext-link>.</p><p>The PN analytical tools rely on two interaction-specific measures, the interaction relevance and interaction stability statistics that identify gene–gene interactions that can be inferred from the prior and experimental data with high confidence. The interaction relevance statistic spans [0,1] where values close to 1 represent interactions that are strongly supported by the data (literature-inferred interactions and/or genomic data) while values close to 0 denote interactions that are only weakly supported. The interaction stability statistic also spans [0,1] and uses <italic>k</italic>-fold cross validation to estimate how strongly the inference of an interaction depends on the initial dataset used to identify it. Values close to 1 represent stable interactions that are inferred irrespective of the precise dataset used to identify them, and values close to 0 represent interactions that are rarely identified and therefore depend strongly on the dataset.</p><p>We also implemented two gene-specific statistics, <italic>R</italic><sup>2</sup> [<italic>R</italic> squared (<xref rid="gkr1050-B35" ref-type="bibr">35</xref>)] and the MCC [Matthews Correlation Coefficient (<xref rid="gkr1050-B36" ref-type="bibr">36</xref>)], that both help to identify genes in the network whose expression can be reliably predicted based on the expression of their parents. The <italic>R</italic><sup>2</sup> prediction score spans [0,1] where values close to 1 represent strong relationship between parent genes and a target gene as estimated by a linear regression model while values close to 0 denote weak association. <italic>R</italic><sup>2</sup> is available for regression-based network inference only since this technique does not require discretization of the gene expression values (<xref rid="gkr1050-B32" ref-type="bibr">32</xref>). The MCC prediction score also spans [0,1] and its interpretation is the same than <italic>R</italic><sup>2</sup> but in a classification framework where expression values are discretized. MCC is particularly suited to assess quality of Bayesian network inference because, in their traditional implementation, Bayesian network inference requires expression data to be discretized.</p></sec><sec sec-type="cases"><title>Use Case 4: developing a collaborative framework for defining networks</title><p>We realized that users might want to share information with colleagues about the networks they are deducing through their analysis. In the PN web application, we have implemented a community-based tool to allow collaborative development of a comprehensive gene interaction network knowledge base. While a considerable amount of information can be derived from structured data sources and text mining analyses, we recognize that expert curation can provide greater data depth and accuracy than automated methods can provide. To this end, we allow users to upload network data sets into the system and to ‘publish’ these so that others can use them.</p></sec></sec><sec><title>WEB INTERFACE</title><sec><title>Architecture of web interface to PN</title><p>The web interface to PN (<ext-link ext-link-type="uri" xlink:href="http://predictivenetworks.org">http://predictivenetworks.org</ext-link>) uses the Groovy/Grails web application framework (<xref rid="gkr1050-B37" ref-type="bibr">37</xref>,<xref rid="gkr1050-B38" ref-type="bibr">38</xref>) and Java 1.6 technologies. The application runs on an Apache Tomcat 6 web application server on a CentOS 5 Linux server. Front-end interactivity makes use of the jQuery 1.3.2 Javascript library. MySQL is used as the backend database system.</p><p>PN is intended to be used for network inference both via the web application user interface and through third-party applications. In addition to the web application, the PN system also includes a RESTful API. For example, a gene symbol query to this API will return a list of all gene interactions involving that gene allowing users to import these PN triples into their own applications.</p></sec><sec><title>Querying PN</title><p>There are a number of starting points on the main PN page (<xref ref-type="fig" rid="gkr1050-F3">Figure 3</xref>). Users can search for a single gene, the interaction between a pair of genes, interactions linking genes in a list and a network inference analysis panel that allows users to upload their gene expression data and a gene list to infer a robust gene interaction network. Users also have the option of creating an account and logging in so that they have access to additional information as well as the option to store and revisit their analytical results and gene sets through ‘<italic>My Page</italic>’.
<fig id="gkr1050-F3" position="float"><label>Figure 3.</label><caption><p>Front page of the PN web application displaying the four entry points: the single gene, single gene–gene interaction and gene list searches, and the network inference analysis panel. The top left panel provides a series of quick links to ensure easy navigation between the different web pages which compose the PN web application.</p></caption><graphic xlink:href="gkr1050f3"></graphic></fig></p></sec><sec><title>Network visualization</title><p>All network visualization is handled through the same basic interface, with a few additional for inferred networks. The primary display presents interactions between genes as a directed graph and provides options to filter interactions so that large graphs remain readable and avoid the ‘hairball’ effect (<xref rid="gkr1050-B39" ref-type="bibr">39</xref>) while remaining more relevant to the problem being studied. Among these options, users can highlight a specific gene and its interactors, select the maximum of number of genes to display (the genes involved in the largest number of triples are selected), the connection degree, filter the interactions by the number of triples that support them, directionality to a target gene (single gene search only) and the contexts in which triple have been identified.</p></sec><sec><title>Collaboration</title><p>Registered users have access to <italic>My Page</italic> through which they are able to upload gene lists, gene expression data as well as their own gene interaction networks to the system. Gene lists and networks can be kept private or shared with a defined group of users.</p></sec><sec><title>Documentation</title><p>All options are thoroughly documented through tooltips that provide context-specific information and options when the user ‘mouses over’ a relevant item. A video tutorial is available directly from the web application and a PDF manual is being prepared describing the site and its use in greater detail.</p></sec><sec><title>Downloading networks</title><p>All data, except users’ private data, are available for download through the page <italic>System Info</italic>. The gene–gene interactions (triples) identified by PN are available as flat files (resource description framework, RDF files). Lists of genes can be downloaded as spreadsheets (comma separated value, CSV, or tab-delimited text files). Network visualization and heatmaps representing network properties and statistics can be exported as portable network graphics (PNG) files. Networks can also be exported as GML files for further analysis.</p></sec><sec><title>Database core attributes</title><p>The database core attributes are listed in <ext-link ext-link-type="uri" xlink:href="http://nar.oxfordjournals.org/cgi/content/full/gkr1050/DC1">Supplementary File S1</ext-link>, in accordance with the BioDBcore standards (<xref rid="gkr1050-B40" ref-type="bibr">40</xref>,<xref rid="gkr1050-B41" ref-type="bibr">41</xref>).</p></sec></sec><sec><title>CASE STUDIES</title><sec sec-type="cases"><title>Case Study 1: search for genes known to interact with a specific gene</title><p>Let's consider that a user wants to retrieve all the genes known to interact with BRCA1, a gene whose mutation is well-established to significantly increase risk of breast cancer (<xref rid="gkr1050-B42" ref-type="bibr">42</xref>). On the front page of the PN web application in the ‘Search for a Gene:’ box, the user can enter the gene symbol, ‘BRCA1’. Since a gene symbol may be ambiguous, if only a gene symbol is being entered a list of alternative gene symbols is proposed while the user is typing.</p><p>Hitting the ‘Search’ button returns a list of possible hits, highlighting gene names. In this case, the user can click on ‘BRCA1’ which brings up the option to ‘View Details’. Selecting this returns detailed information on the gene, including its gene symbol, name, alternative symbol, alternative names and External IDs including EnsEMBL and EntrezGene identifiers. A first degree directed network presenting the genes most commonly reported to interact with BRCA1 is also presented, as is a gene name ‘tag cloud’ and a comprehensive list reporting the triples, their number of occurrences, their context and the primary data source from which they were derived. As noted previously, the network graph can be saved or exported for further analysis. All supporting documentation, including the complete list of triples containing BRCA1 can be downloaded in a variety of formats.</p><p>For BRCA1, PN identified 856 triples, of which 208 were extracted from PubMed abstract and full-text articles and the remainder were annotated in pathway databases. Three genes—BARD1, P53 and RAD51—were reported to interact with BRCA1 in at least 10 triples.</p></sec><sec sec-type="cases"><title>Case Study 2: network analysis of a published gene signature</title><p>There have been thousands of published studies that compare gene expression patterns between various phenotypic conditions. The product of the analysis of the data in these studies is typically a list of genes that the authors of the study found to be significant in distinguishing their experimental groups. For example, we recently discovered a gene signature that is predictive of the mutational status of PIK3CA oncogene in breast cancer (<xref rid="gkr1050-B43" ref-type="bibr">43</xref>). Although the signature is robust and highly predictive, little is known about relationships between the genes themselves and how they interact in the mutated and wild-type PIK3CA phenotypes.</p><p>We used the PN web application to infer a robust gene interaction network among these genes using both known gene–gene interactions and the gene expression data from Loi <italic>et al.</italic> (<xref rid="gkr1050-B43" ref-type="bibr">43</xref>). We first created a user account (only username and email address are required), logged in and went to <italic>My Page</italic>. We started with the ‘Create Analysis’ option and entered the PIK3CA gene list, which we had downloaded from GeneSigDB (<ext-link ext-link-type="uri" xlink:href="http://compbio.dfci.harvard.edu/genesigdb/signaturedetail.jsp?signatureId=20479250-TableS4">http://compbio.dfci.harvard.edu/genesigdb/signaturedetail.jsp?signatureId=20479250-TableS4</ext-link>) (<xref rid="gkr1050-B44" ref-type="bibr">44</xref>), and uploaded a data file that included gene expression data on those 30 genes in the PIK3CA signature measured in 148 breast cancer patients (the top 30 genes of the PIK3CA signature and the gene expression data have been preloaded in the PN web application as examples) (<xref rid="gkr1050-B43" ref-type="bibr">43</xref>,<xref rid="gkr1050-B45" ref-type="bibr">45</xref>). Hitting the ‘Run Analysis’ button launches a network inference, the results of which are then posted to the ‘Results For My Analyses’ section of ‘My Page’.</p><p>Clicking on the name of the analysis brings up a summary and we can further explore the results of the analysis. The topology of the inferred network, and its related statistics can be visualized through directed graphs and heatmaps (<xref ref-type="fig" rid="gkr1050-F4">Figure 4</xref>). The page displaying the topology of the networks helps the user easily identify the interactions that are supported both by the priors (biomedical literature or structured biological databases or both) and the gene expression data, as well as novel interactions deduced in the analysis (<xref ref-type="fig" rid="gkr1050-F4">Figure 4</xref>).
<fig id="gkr1050-F4" position="float"><label>Figure 4.</label><caption><p>Gene interaction network inferred from breast cancer gene expression data and the PIK3CA signature. The network graph in the upper panel allows users to view the topology of the inferred gene interaction network. Each gene–gene interaction is color-coded to represent the evidence supporting it: literature-inferred interactions that are not supported by reported PN triples are colored in red, those inferred from the data only are green, and those supported by both are yellow. In the lower panel a color-coded heatmap allows users to quickly identify clusters of interactions and click on an interaction of interest to highlight it on the network graph.</p></caption><graphic xlink:href="gkr1050f4"></graphic></fig></p><p>For the analysis described here, we find evidence of interactions for >20 of the initial 30 genes, with genes like PITX1, IRS2 or NOTCH2 being highly connected. The user can also view representations of the interaction- and gene-specific statistics and so choose to focus on the parts of the network that are inferred with higher confidence. One can see that, due to the small sample size, many interactions are unstable (stability < 0.5) but that there are also a set of highly stable interactions such as IRS2→PIK3R3 and SCGB2↔A2SCGB1D2 (<xref ref-type="fig" rid="gkr1050-F5">Figure 5</xref>A). By looking at the <italic>R</italic><sup>2</sup> prediction statistics one can see that a third of the genes have good prediction scores, which means that, despite the small sample size, the inferred network model can reasonably predict the expression of these genes based on their parents (<xref ref-type="fig" rid="gkr1050-F5">Figure 5</xref>B).
<fig id="gkr1050-F5" position="float"><label>Figure 5.</label><caption><p>Interaction- and gene-specific statistics for the PIK3CA gene interaction network. The interaction-specific stability scores are represented in (<bold>A</bold>) and can be displayed in the PN application by mousing over the heatmap. One can see that many interactions are unstable (stability < 0.5) meaning that they cannot be confidently inferred from the data. However, some such as SCGB2A2SCGB1D2 are highly stable given the data. The gene-specific <italic>R</italic><sup>2</sup> prediction scores are displayed in (<bold>B</bold>) where one can see that some genes can be accurately predicted given their parents, see SCGB2A2, SCGB1D2, RPL14, PITX1, IRS2, MYC and NOTCH2 for instance.</p></caption><graphic xlink:href="gkr1050f5"></graphic></fig></p></sec></sec><sec><title>SUMMARY AND FUTURE DIRECTIONS</title><p>The Predictive Networks application fills an important need by allowing efficient extraction of contextualized gene–gene interactions from a variety of data sources, including full-text PubMed articles and structured biological databases. It further enables the use of these relationships to infer robust gene interaction networks from high-throughput genomic data. We have implemented these functions in an open-source web application that facilitates query and extraction of such biological networks; the framework we developed could be easily extended by power users to include additional network inference algorithms. Further, PN provides a collaboration framework in which scientists can search, share and curate gene networks.</p><p>The PN web interface will continue to develop and we intend to implement several new features, including allowing users to curate triples identified by the PN text-mining pipeline and share them with other users. We also plan to enrich the network visualization with new layouts (hierarchical or circular network representations, for instance), and to optimize visualization of heatmaps to better assess the high quality subtnetworks within very large networks. Parallelization of our network inference algorithms is also a priority as it will accelerate these computationally intensive analyses. Finally, our hope is to extend network inference methods beyond gene expression data to include other genomic and epigenomic data types.</p></sec><sec><title>LICENSE</title><p>The software used in constructing Predictive Networks is open source software and provided under the Apache License 2.0. All content created by the Predictive Networks application including text mining results, is provided without restriction. Data used within the PN application but derived from third party sources (such as Pathway Commons data) are covered by their own licenses and restrictions.</p></sec><sec><title>SUPPLEMENTARY DATA</title><p><ext-link ext-link-type="uri" xlink:href="http://nar.oxfordjournals.org/cgi/content/full/gkr1050/DC1">Supplementary Data</ext-link> are available at NAR Online: Supplementary Figure 1 and Supplementary References [3,28,29,46–49].</p></sec><sec><title>FUNDING</title><p>Funding for open access charge: <funding-source>National Library of Medicine of the US National Institutes of Health</funding-source> (grant <award-id>1R01LM010129</award-id>).</p><p><italic>Conflict of interest statement</italic>. None declared.</p></sec></body><back><ack><title>ACKNOWLEDGEMENTS</title><p>We thank the Entagen software implementation team, especially Erik Bakke and James Hardwick, and Gerald Papenhausen for their efficient development of the Predictive Networks web application.</p></ack><ref-list><title>REFERENCES</title><ref id="gkr1050-B1"><label>1</label><element-citation publication-type="journal"><person-group person-group-type="author"><name><surname>Spellman</surname><given-names>PT</given-names></name><name><surname>Sherlock</surname><given-names>G</given-names></name><name><surname>Zhang</surname><given-names>MQ</given-names></name><name><surname>Iyer</surname><given-names>VR</given-names></name><name><surname>Anders</surname><given-names>K</given-names></name><name><surname>Eisen</surname><given-names>MB</given-names></name><name><surname>Brown</surname><given-names>PO</given-names></name><name><surname>Botstein</surname><given-names>D</given-names></name><name><surname>Futcher</surname><given-names>B</given-names></name></person-group><article-title>Comprehensive identification of cell cycle-regulated genes of the yeast <italic>Saccharomyces cerevisiae</italic> by microarray hybridization</article-title><source>Mol. 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