IGVFFI2722FGDA

preview

validated

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

File Set

IGVFDS6373YBDI(single-nucleus RNA sequencing assay (10x multiome))

Summary

R1 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

igvf:corces_sequenceFile_RNA_RP011_G8_P060_L005_R1

md5sum

5c5f91775ac004af90ea80015eec3879

Content MD5sum

5bd6a4a264d9785a55f6a96080874a2f

File Size

1.6 GB

Submitted File Name

Multiome_RNA_RP011_G8_L008_P060_S44_L005_R1_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

223HCCLT3

Lane

Sequencing Kit

NovaSeq X Series 10B Reagent Kit

Illumina Read Type

Average Read Length

Read Count

83649282

Samples

1 item

Accession

Type

Sample Terms

Disease Terms

Summary

IGVFSM3747QRCH

MultiplexedSample

cerebellar cortex, middle temporal gyrus, posterior cingulate gyrus, putamen, substantia nigra

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

multiplexed sample: Homo sapiens (male, 53 years) middle temporal gyrus tissue; Homo sapiens (male, 75 years) substantia nigra tissue associated with Parkinson's disease, cerebral amyloid angiopathy; ... and 14 more samples