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IGVFFI8938MAFQ
IGVFFI8938MAFQ
preview
validated
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This object is in preview status. Metadata is subject to change until this object is released.
File Set
IGVFDS7476HGYD
(scRNA-seq)
Summary
I2 reads from sequencing run 2
File Format
fastq
Content Type
reads
Aliases
harinder-singh:multiplexed_perturbation_scRNAseq_20231117_GEX_NGS_LAF6401A8_L003_I2
md5sum
7adbb2c51292db08b9e07dbebe92087a
Content MD5sum
a89bd49fe9ad39d19281d0349a30c233
File Size
893 MB
Submitted File Name
/ix/djishnu/Common_Folder/Pease_Data/20231110_PerturbSeq/2_111723_Hsingh_5Pv2_GEX_LAF6401A8_S24_L003_I2_001.fastq.gz
Checkfiles Version
v17
Attribution
Harinder Singh, University of Pittsburgh
(
HG012041
—
Harinder Singh
)
Sequencing Details
Sequencing Platform
Illumina NovaSeq 6000
Sequencing Run
2
Lane
3
Sequencing Kit
NovaSeq 6000 S4 Reagent Kit v1.5
Illumina Read Type
I2
Average Read Length
10
Read Count
119208109
Samples
1 item
Accession
Type
Sample Terms
Disease Terms
Summary
IGVFSM0805QYBD
MultiplexedSample
B cell
multiplexed sample: Homo sapiens (male) B differentiated cell specimen induced to plasmablast for 4 days; Homo sapiens (male) B differentiated cell specimen induced to plasmablast for 4 days; ... and 10 more samples
Files Derived From This File
1 item
Accession
File Format
Content Type
Summary
Lab
File Size
Upload Status
IGVFFI3750AJCL
h5ad
sparse gene count matrix
cell by gene expression in sparse gene count matrix
Harinder Singh, University of Pittsburgh
835 MB
validated