HG011989

Ian Whaling

Molecular phenotyping of ~100,000 coding variants across Mendelian disease genes

Marc Vidal

HG011972

jesse-engreitz

Jesse Engreitz, Stanford

Frederick Roth

Mikko Taipale

David Hill

Anne Carpenter

audit_ntr_term_id

audit_missing_seqspec

CRISPR FlowFISH screen

TeloHAEC cell line, female, Homo sapiens (sorting details: FACS bin B for 26-50% expression of NOS3) modified with CRISPRi Sp-dCas9-KOX1-KRAB, transfected with a guide library

Chongyon Park

gRNA sequencing for CRISPR interference FlowFISH screen integrating a guide (sgRNA) library targeting sequence variants, transcription start sites in NOS3

IGVFDS2650GXKT

IGVFDS2650GXKT

Sequencing Results (Illumina)

Attribution

IGVFDS2650GXKT

Sequencing Results (Illumina)

Samples

Donors

Related Measurement Sets

Attribution