IGVFFI7782DEGB

released
validated
File Set
IGVFDS0244COUW(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_CCND1_Auxin6hrs-FF2-BinC-PCR3-Rep1_S321
md5sum
a1f514c4e65a5afdbcccc584958373e5
Content MD5sum
8e0d6ae55b0862b8a82f6efc2aa453f5
File Size
36 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/220308B014_CCND1_SSFA2_FAM3C/fastq_trim/CCND1-Auxin6hrs-FF2-BinC-PCR3-Rep1_S321_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Index
GCACATCT:ATTG
Average Read Length
21
Read Count
1631323

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens (sorting details: FACS bin C for 35-45% expression of CCND1) 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

Associated seqspec Files

1 item
Accession
File Format
Content Type
Summary
Lab
File Size
Upload Status
yaml
seqspec
seqspec of IGVFFI7782DEGB
Jesse Engreitz, Stanford
913 B
validated

Attribution