IGVFFI9298IPBX

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

R1 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

gary-hon:LW282C_1_R1

md5sum

2cfd6bb845bf76e61915f1ecf667e50e

Content MD5sum

ef1bbefdc0c897d924387a07afd50013

File Size

206 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_L001_R1_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NextSeq 2000

Sequencing Run

Flowcell ID

AAC7VLGHV

Lane

Illumina Read Type

Average Read Length

Read Count

10561534

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM1288TQKF

InVitroSystem

GM25256 (WTC-11)

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