IGVFFI5187FLEO

preview

validated

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

File Set

IGVFDS2613EUNR(single-nucleus ATAC-seq (10x multiome))

Summary

R2 reads from sequencing run 1

File Format

fastq

Content Type

reads

Aliases

igvf:corces_sequenceFile_ATAC_X048_G5_P049_L001_R2

md5sum

ab508c5b2681b35946d3d99d00af44d0

Content MD5sum

8f8b12b4965dec77b5cca248ca274e96

File Size

4.1 GB

Submitted File Name

Multiome_ATAC_X048_G5_L005_P049_S9_L001_R2_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

Read Count

202612926

Samples

1 item

Accession

Type

Sample Terms

Disease Terms

Summary

IGVFSM6138EUGH

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