IGVFFI0982WORL

preview

validated

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

File Set

IGVFDS8839RSIR(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 2

File Format

fastq

Content Type

reads

Aliases

gary-hon:LW272C_1_R1

md5sum

afd40c338b68c0763e63e0c0ee6a28cb

Content MD5sum

bc356d0fdcba8effb98c672ab13681d6

File Size

1.0 GB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2023/2023-12-22-McDermott-NextSeq.10X/2023-12-22/outs/fastq_path/AAF5CKNM5//LW272C_S6_L001_R1_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NextSeq 2000

Sequencing Run

Flowcell ID

AAF5CKNM5

Lane

Illumina Read Type

Average Read Length

Read Count

51434877

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM1608DJBB

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW272), female, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library