IGVFFI1593YXMS

released
validated
File Set
IGVFDS3914IPWH(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-Auxin6hrs-FF1-BinB-PCR2_Rep1_S118
md5sum
986558513390167a51d17042e3e2164c
Content MD5sum
3657d02b89577aeb59ac86616553cbff
File Size
27 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin6hrs-FF1-BinB-PCR2-Rep1_S118_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Index
TTGAGCCT:TTGA
Average Read Length
21
Read Count
1372957

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens (sorting details: FACS bin B for 10-20% expression of MYC) treated with 1 μM 5-Phenyl-1H-indole-3-acetic acid for 6 hours, modified with AID system targeting RAD21, CRISPRi Sp-dCas9-KOX1-KRAB, 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 IGVFFI1593YXMS
Jesse Engreitz, Stanford
913 B
validated

Attribution