IGVFFI4334TLKF

released
validated
File Set
IGVFDS2059NFJA(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-FF2-BinE-PCR1_Rep1_S29
md5sum
a7d6c0d639f9afa1c2b737f35d2969f3
Content MD5sum
dfb1790f7d8794de5a11ffb924fa74fe
File Size
37 MB
Submitted File Name
/oak/stanford/groups/engreitz/Projects/Cohesin/220819B015_MYC/fastq_trim/MYC-Auxin0hrs-FF2-BinE-PCR1-Rep1_S29_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Index
TCGCCTTG:TGCG
Average Read Length
21
Read Count
1887479

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
HCT116 cell line, male, Homo sapiens (sorting details: FACS bin E for 80-90% expression of MYC) modified with CRISPRi Sp-dCas9-KOX1-KRAB, inactive AID system targeting RAD21, 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 IGVFFI4334TLKF
Jesse Engreitz, Stanford
910 B
validated

Attribution