IGVFFI5436EVPV

preview
validated
This object is in preview status. Metadata is subject to change until this object is released.
File Set
IGVFDS3567LQMB(cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci)
Summary
I2 reads from sequencing run 1
File Format
fastq
Content Type
reads
Aliases
gary-hon:LW282C_2_I2
md5sum
683a3b1458c706357a8f33e86d3fb793
Content MD5sum
594ff95eb25ed81d6777842c0ef12b44
File Size
86 MB
Submitted File Name
/project/GCRB/Hon_lab/shared/data/sequencing_data/2023/2023-10-05-McDermott-NextSeq.10X/2023-10-05/outs/fastq_path/AAC7VLGHV/LW282C_S6_L002_I2_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Flowcell ID
AAC7VLGHV
Lane
2
Illumina Read Type
I2
Average Read Length
10
Read Count
10020826

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
GM25256 (WTC-11) differentiated cell specimen induced to neural stem cell for 20 days (cellular sub pool: subpool_LW282), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library

Attribution