IGVFFI3918UPES

preview

validated

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

File Set

IGVFDS2600XYHD(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:LW283C_1_I2

md5sum

6999660d8a727945285431e00bee2f8a

Content MD5sum

413310d4986b9c1e07653c91676a540d

File Size

106 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/LW283C_S7_L001_I2_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

12583715

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM8464JMJS

InVitroSystem

GM25256 (WTC-11)

GM25256 (WTC-11) differentiated cell specimen induced to neural stem cell for 20 days (cellular sub pool: subpool_LW283), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library