IGVFFI8222NADI

preview

validated

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

File Set

IGVFDS3142DMWW(single-nucleus RNA sequencing assay (10x multiome))

Summary

R2 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

igvf:corces_sequenceFile_RNA_RP031_G2_P080_L007_R2

md5sum

0506d9a88d836cb11f43f34c8c198795

Content MD5sum

97ff45a2ceca9df9cc9af06133a85ddf

File Size

11 GB

Submitted File Name

Multiome_RNA_RP031_G2_L002_P080_S38_L007_R2_001.fastq.gz

Checkfiles Version

v20

Attribution

Ryan Corces, Gladstone Institute UCSF

(

HG012076 — Ansuman Satpathy

)

Sequencing Details

Sequencing Platform

Illumina NovaSeq X

Sequencing Run

Flowcell ID

19NHCA4LE

Lane

Sequencing Kit

NovaSeq X Series 10B Reagent Kit

Illumina Read Type

Average Read Length

151

Read Count

156795528

Samples

1 item

Accession

Type

Sample Terms

Disease Terms

Summary

IGVFSM2932RFCB

MultiplexedSample

posterior cingulate gyrus, putamen, substantia nigra

Alzheimer disease, cerebral amyloid angiopathy, mild cognitive impairment, multiple sclerosis, Parkinson's disease

multiplexed sample: Homo sapiens (male, 78 years) putamen tissue associated with Parkinson's disease, mild cognitive impairment; Homo sapiens (male, 70 years) putamen tissue associated with Parkinson's disease; ... and 6 more samples