IGVFFI7757VRPV

released
validated
File Set
IGVFDS9728LNRU(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-BinA-PCR4_Rep1_S129
md5sum
5a9bf1d5edecf72f79a52ac1d30b65af
Content MD5sum
1cacf08f0549517f2390a0e214dfa769
File Size
19 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin6hrs-FF1-BinA-PCR4-Rep1_S129_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Index
CATAGCGA:TTGA
Average Read Length
21
Read Count
969584

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens (sorting details: FACS bin A for 0-10% 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 IGVFFI7757VRPV
Jesse Engreitz, Stanford
911 B
validated

Attribution