TY - JOUR
T1 - A critical assessment of Mus musculus gene function prediction using integrated genomic evidence
AU - Peña-Castillo, Lourdes
AU - Tasan, Murat
AU - Myers, Chad L.
AU - Lee, Hyunju
AU - Joshi, Trupti
AU - Zhang, Chao
AU - Guan, Yuanfang
AU - Leone, Michele
AU - Pagnani, Andrea
AU - Kim, Wan Kyu
AU - Krumpelman, Chase
AU - Tian, Weidong
AU - Obozinski, Guillaume
AU - Qi, Yanjun
AU - Mostafavi, Sara
AU - Lin, Guan Ning
AU - Berriz, Gabriel F.
AU - Gibbons, Francis D.
AU - Lanckriet, Gert
AU - Qiu, Jian
AU - Grant, Charles
AU - Barutcuoglu, Zafer
AU - Hill, David P.
AU - Warde-Farley, David
AU - Grouios, Chris
AU - Ray, Debajyoti
AU - Blake, Judith A.
AU - Deng, Minghua
AU - Jordan, Michael I.
AU - Noble, William S.
AU - Morris, Quaid
AU - Klein-Seetharaman, Judith
AU - Bar-Joseph, Ziv
AU - Chen, Ting
AU - Sun, Fengzhu
AU - Troyanskaya, Olga G.
AU - Marcotte, Edward M.
AU - Xu, Dong
AU - Hughes, Timothy R.
AU - Roth, Frederick P.
N1 - Funding Information:
Team A (GO, GL, JQ, CG, MJ, and WSN) was supported by NIH award R33 HG003070. Team B (HL, MD, TC, and FS) was supported by NIH/NSF joint mathematical biology initiative DMS-0241102 and NIH P50 HG 002790; HL is supported by the systems biology infrastructure establishment grant provided by Gwangju Institute of Science and Technology in 2008; MD is supported by the National Natural Science Foundation of China (No. 30570425), the National Key Basic Research Project of China (No. 2003CB715903), and Microsoft Research Asia (MSRA). Team C (SM, DW-F, CG, DR, QM) was supported by an NSERC operating grant to QM as well as a Genome Canada grant administered by the Ontario Genomics Institute. Team D (YG, CLM, ZB, and OGT) was partially supported by NIH grant R01 GM071966 and NSF grant IIS-0513552 to OGT and NIGMS Center of Excellence grant P50 GM071508. Team E (WKK, CK, and EMM) was supported by grants from the NIH, NSF, Packard and Welch Foundations. Team F (TJ, CZ, GNL, and DX) was supported by USDA/CSREES-2004-25604-14708 and NSF/ITR-IIS-0407204. Team G (MT, WT, FDG, GFB, and FPR) was supported by NIH grants (HG003224, HG0017115, HL81341, HG004233 and HG004098), by the Keck Foundation, and by NSF TeraGrid resources. Team H (YQ, JK, and ZB) was supported in part by National Science Foundation NSF grants EIA0225656, EIA0225636, CAREER CC044917 and National Institutes of Health NIH grant LM07994-01. Team I (ML and AP) warmly thanks A Vazquez for his support. DPH and JAB were supported by HG002273. LP-C and TRH were supported by a CIHR grant and thank O Meruvia for helping with the design of figures.
PY - 2008/6/27
Y1 - 2008/6/27
N2 - Background: Several years after sequencing the human genome and the mouse genome, much remains to be discovered about the functions of most human and mouse genes. Computational prediction of gene function promises to help focus limited experimental resources on the most likely hypotheses. Several algorithms using diverse genomic data have been applied to this task in model organisms; however, the performance of such approaches in mammals has not yet been evaluated. Results: In this study, a standardized collection of mouse functional genomic data was assembled; nine bioinformatics teams used this data set to independently train classifiers and generate predictions of function, as defined by Gene Ontology (GO) terms, for 21,603 mouse genes; and the best performing submissions were combined in a single set of predictions. We identified strengths and weaknesses of current functional genomic data sets and compared the performance of function prediction algorithms. This analysis inferred functions for 76% of mouse genes, including 5,000 currently uncharacterized genes. At a recall rate of 20%, a unified set of predictions averaged 41% precision, with 26% of GO terms achieving a precision better than 90%. Conclusion: We performed a systematic evaluation of diverse, independently developed computational approaches for predicting gene function from heterogeneous data sources in mammals. The results show that currently available data for mammals allows predictions with both breadth and accuracy. Importantly, many highly novel predictions emerge for the 38% of mouse genes that remain uncharacterized.
AB - Background: Several years after sequencing the human genome and the mouse genome, much remains to be discovered about the functions of most human and mouse genes. Computational prediction of gene function promises to help focus limited experimental resources on the most likely hypotheses. Several algorithms using diverse genomic data have been applied to this task in model organisms; however, the performance of such approaches in mammals has not yet been evaluated. Results: In this study, a standardized collection of mouse functional genomic data was assembled; nine bioinformatics teams used this data set to independently train classifiers and generate predictions of function, as defined by Gene Ontology (GO) terms, for 21,603 mouse genes; and the best performing submissions were combined in a single set of predictions. We identified strengths and weaknesses of current functional genomic data sets and compared the performance of function prediction algorithms. This analysis inferred functions for 76% of mouse genes, including 5,000 currently uncharacterized genes. At a recall rate of 20%, a unified set of predictions averaged 41% precision, with 26% of GO terms achieving a precision better than 90%. Conclusion: We performed a systematic evaluation of diverse, independently developed computational approaches for predicting gene function from heterogeneous data sources in mammals. The results show that currently available data for mammals allows predictions with both breadth and accuracy. Importantly, many highly novel predictions emerge for the 38% of mouse genes that remain uncharacterized.
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U2 - 10.1186/gb-2008-9-s1-s2
DO - 10.1186/gb-2008-9-s1-s2
M3 - Article
C2 - 18613946
AN - SCOPUS:47549116997
SN - 1474-7596
VL - 9
JO - Genome biology
JF - Genome biology
IS - SUPPL. 1
M1 - S2
ER -