IGVFFI1007CYRL

released
validated
File Set
IGVFDS6541EVXL(gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci)
Summary
reads from sequencing run 1
File Format
fastq
Content Type
reads
Aliases
jesse-engreitz:auxiliary_file_CRUDO_MYC-Auxin0hrs-FF2-BinD-PCR1_Rep1_S28
md5sum
8425e25016dffe04765e4641cad27f42
Content MD5sum
aea40e1900ba4d9eb42acb0700beb647
File Size
42 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin0hrs-FF2-BinD-PCR1-Rep1_S28_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Index
CCTATGCC:TGCG
Average Read Length
21
Read Count
2159566

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens (sorting details: FACS bin D for 55-65% expression of MYC) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, transfected with a guide library

Associated seqspec Files

1 item
Accession
File Format
Content Type
Summary
Lab
File Size
Upload Status
yaml
seqspec
seqspec of IGVFFI1007CYRL
Jesse Engreitz, Stanford
911 B
validated

Attribution