IGVFFI5758ILZG

preview

validated

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

File Set

IGVFDS6780UKAY(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:LW421C_6_R1

md5sum

b90a46aedd96eb7b94987e9abdf10914

Content MD5sum

ef8543bd9fed58da1726eb570c5826d4

File Size

4.9 GB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2024/2024-05-01-Novogene-NovaSeq.Hon19_20/HTO//LW421C_S17_L006_R1_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

151

Read Count

78130375

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM3680SAKS

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW421), female, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library