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IGVFFI6046HGLQ
IGVFFI6046HGLQ
preview
validated
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This object is in preview status. Metadata is subject to change until this object is released.
File Set
IGVFDS5867EPVA
(scRNA-seq)
Summary
R2 reads from sequencing run 2
File Format
fastq
Content Type
reads
Aliases
harinder-singh:multiplexed_perturbation_scRNAseq_20240212_GEX_NGS_2_LAF7052A9_L002_R2
md5sum
655e6744795c3a18f17a3018d9fe2379
Content MD5sum
2b6cbdf61b9e33519ee9927855ed0fb7
File Size
18 GB
Submitted File Name
/ix/djishnu/Common_Folder/Pease_Data/20240318_PerturbSeq_2/Singh_021224_2_Pool_5Pv2_GEX_LAF7052A9_S2_L002_R2_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
2
Sequencing Kit
NovaSeq 6000 S4 Reagent Kit v1.5
Illumina Read Type
R2
Average Read Length
90
Read Count
371807553
Samples
1 item
Accession
Type
Sample Terms
Disease Terms
Summary
IGVFSM5472KWSO
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 6 days; ... and 12 more samples
Files Derived From This File
1 item
Accession
File Format
Content Type
Summary
Lab
File Size
Upload Status
IGVFFI3987VJYL
h5ad
sparse gene count matrix
cell by gene expression in sparse gene count matrix
Harinder Singh, University of Pittsburgh
1.2 GB
validated