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Multiplex enCas12a screens detect functional buffering among paralogs otherwise masked in monogenic Cas9 knockout screens.

Merve DedeMegan McLaughlinEiru KimTraver Hart
Published in: Genome biology (2020)
Together, these observations strongly suggest that functionally redundant paralogs represent a targetable set of genetic dependencies that are systematically under-represented among cell-essential genes in monogenic CRISPR-based loss of function screens.
Keyphrases
  • genome wide
  • dna methylation
  • high throughput
  • copy number
  • crispr cas
  • genome editing
  • single cell
  • cell therapy
  • gene expression
  • stem cells