IGVFFI2284PSOB

preview

validated

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

File Set

IGVFDS9367SSNX(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_X048_G7_P050_L002_R1

md5sum

fcda9b2e1baf737e7f27991d9ebaa7b8

Content MD5sum

d772f19c135f1883430249bd907703c0

File Size

13 GB

Submitted File Name

Multiome_RNA_X048_G7_L007_P050_S23_L002_R1_001.fastq.gz

Checkfiles Version

v20

Attribution

Ryan Corces, Gladstone Institute UCSF

(

HG012076 — Ansuman Satpathy

)

Sequencing Details

Sequencing Platform

Illumina NovaSeq 6000

Sequencing Run

Flowcell ID

H7VW3DSX7

Lane

Sequencing Kit

NovaSeq 6000 S4 Reagent Kit v1.5

Illumina Read Type

Average Read Length

101

Read Count

190820134

Samples

1 item

Accession

Type

Sample Terms

Disease Terms

Summary

IGVFSM2062JXFD

MultiplexedSample

posterior cingulate gyrus, substantia nigra

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

multiplexed sample: Homo sapiens (male, 93 years) substantia nigra tissue; Homo sapiens (male, 75 years) substantia nigra tissue associated with Parkinson's disease, mild cognitive impairment; ... and 10 more samples