IGVFFI5042RRSN

released
validated
File Set
IGVFDS4252ROMJ(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-FF1-BinC-PCR3_Rep1_S15
md5sum
087eeeb5fb501eccfdaec7854a265cad
Content MD5sum
9d251a38003671df1b84c527879920a5
File Size
39 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin0hrs-FF1-BinC-PCR3-Rep1_S15_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Index
TCGGAATG:TGCG
Average Read Length
21
Read Count
1991342

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens (sorting details: FACS bin C for 35-45% 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 IGVFFI5042RRSN
Jesse Engreitz, Stanford
910 B
validated

Attribution