IGVFFI7518XBAK

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validated
This object is in preview status. Metadata is subject to change until this object is released.
File Set
IGVFDS2600XYHD(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:LW283C_2_I2
md5sum
2e74e1187642686c02a8efe55d63abba
Content MD5sum
e0803f5b0fb2ad3f531f93042a15c208
File Size
95 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/LW283C_S7_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
11447913

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_LW283), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library

Attribution