IGVFFI8079GYLE

released

validated

File Set

IGVFDS2805FQAD(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-Auxin0hrs-FF1-BinA-PCR4_Rep2_S74

md5sum

73d26dde69b29e7a8564bba9da491c3d

Content MD5sum

8181af9141767d70f761483d99abf3ad

File Size

19 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin0hrs-FF1-BinA-PCR4-Rep2_S74_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

CATAGCGA:TCTC

Average Read Length

Read Count

962173

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM3086DQMC

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin A for 0-10% expression of MYC) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, transfected with a guide library