IGVFFI6603ZNLC

preview

validated

This object is in preview status. Metadata is subject to change until this object is released.

File Set

IGVFDS3465KEWH(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:LW286C_1_R1

md5sum

17f5f2d1977fe50ee3854e2204312c9f

Content MD5sum

40c3dcf4b23b54f5047298680d2306e1

File Size

131 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//LW286C_S5_L001_R1_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NextSeq 2000

Sequencing Run

Flowcell ID

AAF3JCVM5

Lane

Illumina Read Type

Average Read Length

Read Count

6437635

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM2726ORRN

InVitroSystem

GM25256 (WTC-11)

GM25256 (WTC-11) cell line (cellular sub pool: subpool_LW286), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library