IGVFFI1692PBQW

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

R2 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

gary-hon:LW282C_2_R2

md5sum

cef410276aae8d92aefb77022d06b3ec

Content MD5sum

5aec7c5ed6bea45b4ee25a753b52536b

File Size

393 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_R2_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

10020826

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