IGVFFI1717GCIU

released

validated

File Set

IGVFDS4450DYPE(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_FAM3C_Auxin0hrs-FF2-BinC-PCR4-Rep1_S183

md5sum

57c741ff6375e91ca15baef8161d7012

Content MD5sum

745db7adf0f49eab8d8acbc350e204ae

File Size

33 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220308B014_CCND1_SSFA2_FAM3C/fastq_trim/FAM3C-Auxin0hrs-FF2-BinC-PCR4-Rep1_S183_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

CGTTACCA:ATTG

Average Read Length

Read Count

1522346

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM0890WDDX

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin C for 35-45% expression of FAM3C) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, transfected with a guide library