Functional Characterization Experiment summary for ENCSR831DXR

doi:10.17989/ENCSR831DXR

Summary

Status
released
Assay
FACS CRISPR screen
Biosample summary
Homo sapiens K562 genetically modified (insertion) using transduction (low MOI), using CRISPR cutting (sgRNA) for MYC locus
Biosample Type
cell line
Perturbation type
CRISPR cutting
Tiling modality
peak tiling
Examined loci
MYC (0-10%)
CRISPR screen readout
endogenous protein Sort-seq
Replication type
isogenic
Description
CRISPR screen targeting candidate CREs following FACS low
Treatments
Puromycin (CHEBI:17939)
Nucleic acid type
DNA
Controls
Elements references
Elements cloning
ENCSR903VDF

Attribution

ENCODE4 project
Lab
Yin Shen, UCSF
Award
UM1HG009402 (Yin Shen, UCSF)
Project
ENCODE
Aliases
yin-shen:DCC_K562_MYC_GFP_MYC_Screening_FACS_0-10perCent_Experiment
Date released
August 30, 2021
Functional Characterization Series
ENCSR261PJJ 

Isogenic replicates

Isogenic replicate
Technical replicate
Summary
Biosample
Modifications
Library
21Homo sapiens K562 cell line genetically modified (insertion) using transduction (low MOI), genetically modified using CRISPR cutting (sgRNA) 10 days after the sample was treated with PuromycinENCBS497SIFENCGM063WJB, ENCGM885GEZENCLB812DBE
11Homo sapiens K562 cell line genetically modified (insertion) using transduction (low MOI), genetically modified using CRISPR cutting (sgRNA) 10 days after the sample was treated with PuromycinENCBS973SVCENCGM063WJB, ENCGM885GEZENCLB375TRS