Genome-Wide Analysis of Haploinsufficiency in Human Embryonic Stem Cells
Ontology highlight
ABSTRACT: Establishment of a heterozygous genome-wide loss-of-function CRISPR library for studying haploinsufficiency in human embryonic stem cells.
INSTRUMENT(S): NextSeq 500
ORGANISM(S): Homo sapiens
SUBMITTER: Roni Sarel Gallily
PROVIDER: E-MTAB-11464 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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