IGVFFI9696NSTM

released

validated

File Set

IGVFDS1369IMLU(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-FF1-BinF-PCR4-Rep1_S66

md5sum

dcab3e3d6ef68e6cb2c13bf9068d6b85

Content MD5sum

5da263b913417fd5e39cefcffcc223d0

File Size

25 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220308B014_CCND1_SSFA2_FAM3C/fastq_trim/SSFA2-Auxin0hrs-FF1-BinF-PCR4-Rep1_S66_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

TTCGCTGA:GCCA

Average Read Length

Read Count

1140699

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM4326ZGNE

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin F for 80-100% expression of SSFA2) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, transfected with a guide library