IGVFFI1300PPWH

preview

validated

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

File Set

IGVFDS0559WMGB(Parse SPLiT-seq)

Summary

R1 reads from sequencing run 4

File Format

fastq

Content Type

reads

Aliases

maya-kasowski:Parse_P2_scRNA_sublibrary4_lane2_R1

md5sum

0ecfcd4dbedb4f6db0d2e1e01bcffbb4

Content MD5sum

9485233355dc7811e7020817efa1aecb

File Size

9.3 GB

Submitted File Name

/users/shouvikm/data/Parse/P2/usftp21.novogene.com/01.RawData/P2_SL4/P2_SL4_CKDL230018051-1A_225LMWLT3_L2_1.fq.gz

Checkfiles Version

v17

Attribution

Maya Kasowski, Stanford

(

HG012076 — Ansuman Satpathy

)

Sequencing Details

Sequencing Platform

Illumina NovaSeq X Plus

Sequencing Run

Lane

Sequencing Kit

NovaSeq X Series 25B Reagent Kit

Illumina Read Type

Average Read Length

150

Read Count

160039792

Samples

1 item

Accession

Type

Sample Terms

Disease Terms

Summary

IGVFSM4252CQLW

MultiplexedSample

bone marrow, umbilical cord blood

multiplexed sample: Homo sapiens bone marrow cell; Homo sapiens umbilical cord blood cell; ... and 12 more samples