| Literature DB >> 28988802 |
Mehmet Gönen1, Barbara A Weir2, Glenn S Cowley3, Francisca Vazquez4, Yuanfang Guan5, Alok Jaiswal6, Masayuki Karasuyama7, Vladislav Uzunangelov8, Tao Wang9, Aviad Tsherniak2, Sara Howell10, Daniel Marbach11, Bruce Hoff12, Thea C Norman12, Antti Airola13, Adrian Bivol8, Kerstin Bunte14, Daniel Carlin15, Sahil Chopra16, Alden Deran8, Kyle Ellrott17, Peddinti Gopalacharyulu6, Kiley Graim8, Samuel Kaski18, Suleiman A Khan6, Yulia Newton8, Sam Ng8, Tapio Pahikkala13, Evan Paull8, Artem Sokolov8, Hao Tang19, Jing Tang6, Krister Wennerberg6, Yang Xie20, Xiaowei Zhan9, Fan Zhu5, Tero Aittokallio21, Hiroshi Mamitsuka22, Joshua M Stuart8, Jesse S Boehm2, David E Root23, Guanghua Xiao24, Gustavo Stolovitzky25, William C Hahn26, Adam A Margolin27.
Abstract
We report the results of a DREAM challenge designed to predict relative genetic essentialities based on a novel dataset testing 98,000 shRNAs against 149 molecularly characterized cancer cell lines. We analyzed the results of over 3,000 submissions over a period of 4 months. We found that algorithms combining essentiality data across multiple genes demonstrated increased accuracy; gene expression was the most informative molecular data type; the identity of the gene being predicted was far more important than the modeling strategy; well-predicted genes and selected molecular features showed enrichment in functional categories; and frequently selected expression features correlated with survival in primary tumors. This study establishes benchmarks for gene essentiality prediction, presents a community resource for future comparison with this benchmark, and provides insights into factors influencing the ability to predict gene essentiality from functional genetic screens. This study also demonstrates the value of releasing pre-publication data publicly to engage the community in an open research collaboration.Entities:
Keywords: cancer genomics; community challenge; crowdsourcing; functional screen; machine learning; oncogene
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Year: 2017 PMID: 28988802 PMCID: PMC5814247 DOI: 10.1016/j.cels.2017.09.004
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304