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author Venkatesan, Kavitha
Rual, Jean-François
Vazquez, Alexei
Stelzl, Ulrich
Lemmens, Irma
Hirozane-Kishikawa, Tomoko
Hao, Tong
Zenkner, Martina
Xin, Xiaofeng
Goh, Kwang-II
Yildirim, Muhammed A
Simonis, Nicolas
Heinzmann, Kathrin
Gebreab, Fana
Sahalie, Julie M
Cevik, Sebiha
Simon, Christophe
de Smet, Anne-Sophie
Dann, Elizabeth
Smolyar, Alex
Vinayagam, Arunachalam
Yu, Haiyuan
Szeto, David
Borick, Heather
Dricot, Amélie
Klitgord, Niels
Murray, Ryan R
Lin, Chenwei
Lalowski, Maciej
Timm, Jan
Rau, Kirstin
Boone, Charles
Braun, Pascal
Cusick, Michael E
Roth, Frederick P
Hill, David E
Tavernier, Jan
Wanker, Erich E
Barabási, Albert-László
Vidal, Marc
author_facet Venkatesan, Kavitha
Rual, Jean-François
Vazquez, Alexei
Stelzl, Ulrich
Lemmens, Irma
Hirozane-Kishikawa, Tomoko
Hao, Tong
Zenkner, Martina
Xin, Xiaofeng
Goh, Kwang-II
Yildirim, Muhammed A
Simonis, Nicolas
Heinzmann, Kathrin
Gebreab, Fana
Sahalie, Julie M
Cevik, Sebiha
Simon, Christophe
de Smet, Anne-Sophie
Dann, Elizabeth
Smolyar, Alex
Vinayagam, Arunachalam
Yu, Haiyuan
Szeto, David
Borick, Heather
Dricot, Amélie
Klitgord, Niels
Murray, Ryan R
Lin, Chenwei
Lalowski, Maciej
Timm, Jan
Rau, Kirstin
Boone, Charles
Braun, Pascal
Cusick, Michael E
Roth, Frederick P
Hill, David E
Tavernier, Jan
Wanker, Erich E
Barabási, Albert-László
Vidal, Marc
author_sort Venkatesan, Kavitha
collection PubMed
description Several attempts have been made at systematically mapping protein-protein interaction, or “interactome” networks. However, it remains difficult to assess the quality and coverage of existing datasets. We describe a framework that uses an empirically-based approach to rigorously dissect quality parameters of currently available human interactome maps. Our results indicate that high-throughput yeast two-hybrid (HT-Y2H) interactions for human are superior in precision to literature-curated interactions supported by only a single publication, suggesting that HT-Y2H is suitable to map a significant portion of the human interactome. We estimate that the human interactome contains ~130,000 binary interactions, most of which remain to be mapped. Similar to estimates of DNA sequence data quality and genome size early in the human genome project, estimates of protein interaction data quality and interactome size are critical to establish the magnitude of the task of comprehensive human interactome mapping and to illuminate a path towards this goal.
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spelling pubmed-28725612010-05-18 An empirical framework for binary interactome mapping Venkatesan, Kavitha Rual, Jean-François Vazquez, Alexei Stelzl, Ulrich Lemmens, Irma Hirozane-Kishikawa, Tomoko Hao, Tong Zenkner, Martina Xin, Xiaofeng Goh, Kwang-II Yildirim, Muhammed A Simonis, Nicolas Heinzmann, Kathrin Gebreab, Fana Sahalie, Julie M Cevik, Sebiha Simon, Christophe de Smet, Anne-Sophie Dann, Elizabeth Smolyar, Alex Vinayagam, Arunachalam Yu, Haiyuan Szeto, David Borick, Heather Dricot, Amélie Klitgord, Niels Murray, Ryan R Lin, Chenwei Lalowski, Maciej Timm, Jan Rau, Kirstin Boone, Charles Braun, Pascal Cusick, Michael E Roth, Frederick P Hill, David E Tavernier, Jan Wanker, Erich E Barabási, Albert-László Vidal, Marc Nat Methods Article Several attempts have been made at systematically mapping protein-protein interaction, or “interactome” networks. However, it remains difficult to assess the quality and coverage of existing datasets. We describe a framework that uses an empirically-based approach to rigorously dissect quality parameters of currently available human interactome maps. Our results indicate that high-throughput yeast two-hybrid (HT-Y2H) interactions for human are superior in precision to literature-curated interactions supported by only a single publication, suggesting that HT-Y2H is suitable to map a significant portion of the human interactome. We estimate that the human interactome contains ~130,000 binary interactions, most of which remain to be mapped. Similar to estimates of DNA sequence data quality and genome size early in the human genome project, estimates of protein interaction data quality and interactome size are critical to establish the magnitude of the task of comprehensive human interactome mapping and to illuminate a path towards this goal. 2008-12-07 2009-01 /pmc/articles/PMC2872561/ /pubmed/19060904 http://dx.doi.org/10.1038/nmeth.1280 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Venkatesan, Kavitha
Rual, Jean-François
Vazquez, Alexei
Stelzl, Ulrich
Lemmens, Irma
Hirozane-Kishikawa, Tomoko
Hao, Tong
Zenkner, Martina
Xin, Xiaofeng
Goh, Kwang-II
Yildirim, Muhammed A
Simonis, Nicolas
Heinzmann, Kathrin
Gebreab, Fana
Sahalie, Julie M
Cevik, Sebiha
Simon, Christophe
de Smet, Anne-Sophie
Dann, Elizabeth
Smolyar, Alex
Vinayagam, Arunachalam
Yu, Haiyuan
Szeto, David
Borick, Heather
Dricot, Amélie
Klitgord, Niels
Murray, Ryan R
Lin, Chenwei
Lalowski, Maciej
Timm, Jan
Rau, Kirstin
Boone, Charles
Braun, Pascal
Cusick, Michael E
Roth, Frederick P
Hill, David E
Tavernier, Jan
Wanker, Erich E
Barabási, Albert-László
Vidal, Marc
An empirical framework for binary interactome mapping
title An empirical framework for binary interactome mapping
title_full An empirical framework for binary interactome mapping
title_fullStr An empirical framework for binary interactome mapping
title_full_unstemmed An empirical framework for binary interactome mapping
title_short An empirical framework for binary interactome mapping
title_sort empirical framework for binary interactome mapping
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872561/
https://www.ncbi.nlm.nih.gov/pubmed/19060904
http://dx.doi.org/10.1038/nmeth.1280
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