IGVFFI7816MRXM

released

validated

File Set

IGVFDS5772WTGS(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-FF1-BinF-PCR2-Rep1_S144

md5sum

ac97e2a9e8d373542f7bba755e6847f5

Content MD5sum

412ef2a1a00486e8dadd2cbe3d03a557

File Size

24 MB

Submitted File Name

/oak/stanford/groups/engreitz/Projects/Cohesin/220308B014_CCND1_SSFA2_FAM3C/fastq_trim/FAM3C-Auxin6hrs-FF1-BinF-PCR2-Rep1_S144_R1_001.fastq.gz

Sequencing Details

Sequencing Platform

Illumina HiSeq 2500

Sequencing Run

Index

TAATGAAC:CCAG

Average Read Length

Read Count

1108996

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM2608ULOG

InVitroSystem

HCT116

HCT116 cell line, male, Homo sapiens (sorting details: FACS bin F for 80-100% 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