IGVFFI7633XNAY

released

validated

File Set

IGVFDS1012DWQM(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_Auxin6hrs-FF2-BinB-PCR4-Rep1_S206

md5sum

a4e0b531c1c257baed84a7ba5847f01e

Content MD5sum

9f7039e46ac5c217d72c0c7050b9d2ca

File Size

21 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220308B014_CCND1_SSFA2_FAM3C/fastq_trim/FAM3C-Auxin6hrs-FF2-BinB-PCR4-Rep1_S206_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

TATCCAGG:ATTG

Average Read Length

Read Count

952282

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM9676AELV

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin B for 10-20% expression of FAM3C) treated with 1 μM 5-Phenyl-1H-indole-3-acetic acid for 6 hours, modified with AID system targeting RAD21, CRISPRi Sp-dCas9-KOX1-KRAB, transfected with a guide library