Display Settings:

Format

Send to:

Choose Destination
Accession: PRJNA342101 ID: 342101

Homo sapiens (human)

Homo sapiens Raw sequence reads

See Genome Information for Homo sapiens
Using whole genome sequencing (WGS) to detect the causal mutations of Alstrom syndrome.
AccessionPRJNA342101
Data TypeRaw sequence reads, Genome sequencing, Variation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 7-Sep-2016
Fudan University
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments8
Other datasets
BioSample4
SRA Data Details
ParameterValue
Data volume, Gbases441
Data volume, Tbytes0.30

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center