IGVFFI0713WITI

preview

validated

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

File Set

IGVFDS2549GCKW(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:LW281C_2_R1

md5sum

bd4b6fec94de635611219cbaeaac220b

Content MD5sum

d71c2f7d0e30f11ea7aa55bd585cc4e2

File Size

207 MB

Submitted File Name

/project/GCRB/Hon_lab/shared/data/sequencing_data/2023/2023-10-05-McDermott-NextSeq.10X/2023-10-05/outs/fastq_path/AAC7VLGHV/LW281C_S5_L002_R1_001.fastq.gz

Checkfiles Version

Legacy version of checkfiles

Sequencing Details

Sequencing Platform

Illumina NextSeq 2000

Sequencing Run

Flowcell ID

AAC7VLGHV

Lane

Illumina Read Type

Average Read Length

Read Count

10498328

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM0956HKRJ

InVitroSystem

GM25256 (WTC-11)

GM25256 (WTC-11) differentiated cell specimen induced to neural stem cell for 20 days (cellular sub pool: subpool_LW281), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library