4.5 Article

scMAGeCK links genotypes with multiple phenotypes in single-cell CRISPR screens

期刊

GENOME BIOLOGY
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13059-020-1928-4

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资金

  1. NIH/NHGRI [R01-HG-010753]
  2. Pharmaceutical Research and Manufacturers of American Foundation (PhRMA)
  3. Center of Genetic Medicine Research and Gilbert Family NF1 Institute at the Children's National Medical Center
  4. National Key Research and Development Program of China [2018YFA0107100, 2018YFA0107103, 2018YFC1005002]
  5. National Natural Science Foundation projects of China [91857116, 31871453]
  6. Zhejiang Natural Science Foundation projects of China [LR19C120001]

向作者/读者索取更多资源

We present scMAGeCK, a computational framework to identify genomic elements associated with multiple expression-based phenotypes in CRISPR/Cas9 functional screening that uses single-cell RNA-seq as readout. scMAGeCK outperforms existing methods, identifies genes and enhancers with known and novel functions in cell proliferation, and enables an unbiased construction of genotype-phenotype network. Single-cell CRISPR screening on mouse embryonic stem cells identifies key genes associated with different pluripotency states. Applying scMAGeCK on multiple datasets, we identify key factors that improve the power of single-cell CRISPR screening. Collectively, scMAGeCK is a novel tool to study genotype-phenotype relationships at a single-cell level.

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