TY - JOUR
T1 - ScreenBEAM
T2 - A novel meta-analysis algorithm for functional genomics screens via Bayesian hierarchical modeling
AU - Yu, Jiyang
AU - Silva, Jose
AU - Califano, Andrea
N1 - Publisher Copyright:
© 2015 The Author 2015. Published by Oxford University Press. All rights reserved.
PY - 2016/1/15
Y1 - 2016/1/15
N2 - Motivation: Functional genomics (FG) screens, using RNAi or CRISPR technology, have become a standard tool for systematic, genome-wide loss-of-function studies for therapeutic target discovery. As in many large-scale assays, however, off-target effects, variable reagents' potency and experimental noise must be accounted for appropriately control for false positives. Indeed, rigorous statistical analysis of high-throughput FG screening data remains challenging, particularly when integrative analyses are used to combine multiple sh/sgRNAs targeting the same gene in the library. Method: We use large RNAi and CRISPR repositories that are publicly available to evaluate a novel meta-analysis approach for FG screens via Bayesian hierarchical modeling, Screening Bayesian Evaluation and Analysis Method (ScreenBEAM). Results: Results from our analysis show that the proposed strategy, which seamlessly combines all available data, robustly outperforms classical algorithms developed for microarray data sets as well as recent approaches designed for next generation sequencing technologies. Remarkably, the ScreenBEAM algorithm works well even when the quality of FG screens is relatively low, which accounts for about 80-95% of the public datasets. Availability and implementation: R package and source code are available at: https://github.com/jyyu/ScreenBEAM. Contact:, [email protected], [email protected] Supplementary information: Supplementary data are available at Bioinformatics online.
AB - Motivation: Functional genomics (FG) screens, using RNAi or CRISPR technology, have become a standard tool for systematic, genome-wide loss-of-function studies for therapeutic target discovery. As in many large-scale assays, however, off-target effects, variable reagents' potency and experimental noise must be accounted for appropriately control for false positives. Indeed, rigorous statistical analysis of high-throughput FG screening data remains challenging, particularly when integrative analyses are used to combine multiple sh/sgRNAs targeting the same gene in the library. Method: We use large RNAi and CRISPR repositories that are publicly available to evaluate a novel meta-analysis approach for FG screens via Bayesian hierarchical modeling, Screening Bayesian Evaluation and Analysis Method (ScreenBEAM). Results: Results from our analysis show that the proposed strategy, which seamlessly combines all available data, robustly outperforms classical algorithms developed for microarray data sets as well as recent approaches designed for next generation sequencing technologies. Remarkably, the ScreenBEAM algorithm works well even when the quality of FG screens is relatively low, which accounts for about 80-95% of the public datasets. Availability and implementation: R package and source code are available at: https://github.com/jyyu/ScreenBEAM. Contact:, [email protected], [email protected] Supplementary information: Supplementary data are available at Bioinformatics online.
UR - http://www.scopus.com/inward/record.url?scp=84959930865&partnerID=8YFLogxK
U2 - 10.1093/bioinformatics/btv556
DO - 10.1093/bioinformatics/btv556
M3 - Article
C2 - 26415723
AN - SCOPUS:84959930865
SN - 1367-4803
VL - 32
SP - 260
EP - 267
JO - Bioinformatics
JF - Bioinformatics
IS - 2
ER -