IGVFFI5709SYEW

preview

validated

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

File Set

IGVFDS3774FYIW(cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci)

Summary

I1 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

gary-hon:LW433C_6_I1

md5sum

96b2cfc2668b8ac62f33c9d8033a1eb8

Content MD5sum

a739157963a8163d9e670dc4109849ad

File Size

533 MB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2024/2024-05-01-Novogene-NovaSeq.Hon19_20/HTO//LW433C_S27_L006_I1_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NovaSeq 6000

Sequencing Run

Flowcell ID

227C7WLT4

Lane

Sequencing Kit

NovaSeq X Series 25B Reagent Kit

Illumina Read Type

Average Read Length

Read Count

81419276

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM1513DHGW

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW433), female, Homo sapiens modified with CRISPRi Sp-dCas9, transfected with a guide library