IGVFFI7180TCQN

preview

validated

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

File Set

IGVFDS2693DPLW(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:LW284C_2_I2

md5sum

b5991309783427592eea657c82b30f75

Content MD5sum

71b6b8ea9dc67cd8446a1826c0704f94

File Size

85 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/LW284C_S8_L002_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

10360767

Samples

1 item

Accession

Type

Sample Terms

Summary

IGVFSM2597WGYB

InVitroSystem

GM25256 (WTC-11)

GM25256 (WTC-11) differentiated cell specimen induced to neural stem cell for 20 days (cellular sub pool: subpool_LW284), male, Homo sapiens modified with CRISPRi Sp-dCas9, transduced (lentivirus) with a guide library