IGVFFI3021FRGV

preview

validated

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

File Set

IGVFDS1340IBKW(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:LW434C_6_R1

md5sum

0763022a65109903c0a76ce131254d40

Content MD5sum

ae81aba8f6446af96dd130a2b47f508f

File Size

4.5 GB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2024/2024-05-01-Novogene-NovaSeq.Hon19_20/HTO//LW434C_S28_L006_R1_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

151

Read Count

71603025

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM8133YEXK

InVitroSystem

H9 differentiated cell specimen induced to cardiac muscle cell for 12 days (cellular sub pool: subpool_LW434), female, Homo sapiens modified with CRISPRi Sp-dCas9, transfected with a guide library