IGVFFI6591FOMG

released
validated
File Set
IGVFDS8748OHPQ(gRNA sequencing for mixed CRISPR TAP-seq integrating a guide (sgRNA) library targeting accessible genome regions in 29 genomic loci)
Summary
R2 reads from sequencing run 1
File Format
fastq
Content Type
reads
Aliases
jesse-engreitz:auxiliary_files_CRUDO_TAPseq-Auxin0hrs-Rep2_S3_R2
md5sum
09195bab61bfb92222d5105ebcccee5a
Content MD5sum
107a4958c2f3d498a61145c29decfda7
File Size
140 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/221224_Cohesin_TAPseq_v2/221219_P044_cohesin_tapseq_v2/outs/fastq_path/L379_S2_L003_R2_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Lane
3
Illumina Read Type
R2
Average Read Length
90
Read Count
3196495

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 IGVFFI8825PYZU, IGVFFI1717NNGG, IGVFFI6591FOMG
Jesse Engreitz, Stanford
1.2 KB
validated

Attribution