Open AccessA method for benchmarking genetic screens reveals a predominant mitochondrial bias
Author(s) -
Rahman Mahfuzur,
Billmann Maximilian,
Costanzo Michael,
Aregger Michael,
Tong Amy H Y,
Chan Katherine,
Ward Henry N,
Brown Kevin R,
Andrews Brenda J,
Boone Charles,
Moffat Jason,
Myers Chad L
Publication year - 2021
Publication title -
molecular systems biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.523
H-Index - 148
ISSN - 1744-4292
DOI - 10.15252/msb.202010013
Subject(s) - biology , benchmarking , computational biology , genetics , mitochondrial dna , evolutionary biology , gene , marketing , business
We present FLEX (Functional evaluation of experimental perturbations), a pipeline that leverages several functional annotation resources to establish reference standards for benchmarking human genome‐wide CRISPR screen data and methods for analyzing them. FLEX provides a quantitative measurement of the functional information captured by a given gene‐pair dataset and a means to explore the diversity of functions captured by the input dataset. We apply FLEX to analyze data from the diverse cell line screens generated by the DepMap project. We identify a predominant mitochondria‐associated signal within co‐essentiality networks derived from these data and explore the basis of this signal. Our analysis and time‐resolved CRISPR screens in a single cell line suggest that the variable phenotypes associated with mitochondria genes across cells may reflect screen dynamics and protein stability effects rather than genetic dependencies. We characterize this functional bias and demonstrate its relevance for interpreting differential hits in any CRISPR screening context. More generally, we demonstrate the utility of the FLEX pipeline for performing robust comparative evaluations of CRISPR screens or methods for processing them.