IGVFFI6952RHQM

released

validated

File Set

IGVFDS4701YCEL(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-BinB-PCR1_Rep1_S2

md5sum

35f070811f56ff7fb00893abdf911b67

Content MD5sum

c49753d4932628649825a600caf56d6e

File Size

27 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin0hrs-FF1-BinB-PCR1-Rep1_S2_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

CATGCTTA:TGCG

Average Read Length

Read Count

1360310

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM3954RGXF

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin B for 10-20% expression of MYC) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, transfected with a guide library