IGVFFI1578SEWC

preview

validated

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

File Set

IGVFDS7977FNRB(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:LW273C_1_R1

md5sum

2ac8efcf39212fd72a0bfc0d94cdd8b3

Content MD5sum

88f64aaaac7b0f64820377852705bd18

File Size

654 MB

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//LW273C_S11_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

34467058

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM1063UQVF

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW273), female, Homo sapiens modified with CRISPRi Sp-dCas9, transfected with a guide library