IGVFFI7072KBGQ

preview

validated

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

File Set

IGVFDS1760WHSE(cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci)

Summary

I2 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

gary-hon:LW422C_6_I2

md5sum

7201954e3fbeb52e65e5c3df175b16a7

Content MD5sum

898a736c07febc331825f2506dab78a3

File Size

465 MB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2024/2024-05-01-Novogene-NovaSeq.Hon19_20/HTO//LW422C_S18_L006_I2_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NovaSeq X Plus

Sequencing Run

Flowcell ID

227C7WLT4

Lane

Sequencing Kit

NovaSeq X Series 25B Reagent Kit

Illumina Read Type

Average Read Length

Read Count

69597183

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM8986CPUS

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW422), female, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library