IGVFFI7707CNCP

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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_1_I2
md5sum
18a51d23d029a2d4765964ecdcf9bab1
Content MD5sum
777de8abd713c01f49cb29050021a32c
File Size
92 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_L001_I2_001.fastq.gz

Sequencing Details

Sequencing Platform
Sequencing Run
1
Flowcell ID
AAC7VLGHV
Lane
1
Illumina Read Type
I2
Average Read Length
10
Read Count
11104532

Samples

1 item
Accession
Type
Sample Terms
Summary
InVitroSystem
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

Attribution