Modeling Heterogenous Outcomes in Functional Genetic Screens Using Single-cell Genomics as Readouts

NIH RePORTER · NIH · R01 · $268,752 · view on reporter.nih.gov ↗

Abstract

Modeling Heterogenous Outcomes in Functional Genetic Screens Using Single-cell Genomics as Readouts This supplementary request seeks to advance the analysis of single-cell CRISPR screening datasets by developing novel computational models to address the challenge of heterogeneous transcriptome responses upon perturbing the same gene. It falls within the scope of the parent award to develop algorithms for functional genetic screens, but proposes to follow up on unanticipated results (single-cell CRISPR screen) and enhance this direction, which is unexpectedly productive, as is demonstrated in preliminary results. Specifically, we aim to: (1) build a model to detect heterogeneous expression patterns in Perturb-seq assays, l, and (2) extend the model to other dataset types, including pooled single-cell and bulk transcriptomics datasets from various gene perturbations. This work will significantly enhance our understanding of genotype-phenotype relationships at the single-cell level, with broad applications in cancer research, virology, and gene regulation.

Key facts

NIH application ID
10837914
Project number
3R01HG010753-05S1
Recipient
CHILDREN'S RESEARCH INSTITUTE
Principal Investigator
Wei Li
Activity code
R01
Funding institute
NIH
Fiscal year
2023
Award amount
$268,752
Award type
3
Project period
2019-08-08 → 2025-05-31