IGVFFI2893MYCT

released
validated
File Set
IGVFDS7135ULJC(mixed CRISPR TAP-seq integrating a guide (sgRNA) library targeting accessible genome regions in 29 genomic loci)
Summary
R1 reads from sequencing run 1
File Format
fastq
Content Type
reads
Aliases
jesse-engreitz:measurement_files_CRUDO_TAPseq-Auxin0hrs-Rep2_S2_R1
md5sum
11cd74583b2a219daf81796208c1dbbc
Content MD5sum
7181750f92879424ab7919093b4769b5
File Size
390 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/221224_Cohesin_TAPseq_v2/221219_P044_cohesin_tapseq_v2/outs/fastq_path/L378_S1_L002_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Lane
2
Illumina Read Type
R1
Average Read Length
28
Read Count
15976428

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens 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 IGVFFI2893MYCT, IGVFFI7624ITNU, IGVFFI4178KSHJ
Jesse Engreitz, Stanford
1.0 KB
validated

Attribution