IGVFFI1799FWCW

preview
validated
This object is in preview status. Metadata is subject to change until this object is released.
File Set
IGVFDS9718OGWQ(cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci)
Summary
R1 reads from sequencing run 1
File Format
fastq
Content Type
reads
Aliases
gary-hon:LW288C_1_R1
md5sum
716aeb0b401f76204753684b769f60a3
Content MD5sum
ebafd5a999ea1f9a122c97df02e82ee8
File Size
304 MB
Submitted File Name
/project/GCRB/Hon_lab/shared/data/sequencing_data/2023/2023-11-03-McDermott-NextSeq.10X.run2.10X/2023-11-03/outs/fastq_path/AAF3JCVM5//LW288C_S7_L001_R1_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Flowcell ID
AAF3JCVM5
Lane
1
Illumina Read Type
R1
Average Read Length
28
Read Count
15063903

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
GM25256 (WTC-11) cell line (cellular sub pool: subpool_LW288), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library

Attribution