IGVFFI3468FNAC

released

validated

File Set

IGVFDS5686BCWV(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_SSFA2-Auxin0hrs-FF2-BinD-PCR4-Rep1_S76

md5sum

3cffe2258f8dd944bd41344d1ed5c0de

Content MD5sum

e9068b749a3bef6bb63c34efe0d6f212

File Size

24 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220308B014_CCND1_SSFA2_FAM3C/fastq_trim/SSFA2-Auxin0hrs-FF2-BinD-PCR4-Rep1_S76_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

ATTATGTT:GCCA

Average Read Length

Read Count

1101216

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM0599CFOW

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin D for 55-65% expression of SSFA2) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, transfected with a guide library