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Accession: PRJNA290300 ID: 290300

Homo sapiens (human)

CSER: The MedSeq Project

See Genome Information for Homo sapiens
Whole genome sequencing (WGS) and whole exome sequencing (WES) services are currently available to and being utilized by physicians and their patients in both research and clinical settings, and recently to anyone in the general public via direct-to-consumer companies. But the widespread availability and use of WGS and WES in the practice of clinical medicine is imminent. In the very near future, sequencing of individual genomes will be inexpensive and ubiquitous, and patients will be looking to the medical establishment for interpretations, insight and advice to improve their health. Developing standards and procedures for the use of WGS information in clinical medicine is an urgent need, but there are numerous obstacles related to integrity and storage of WGS data, interpretation and responsible clinical integration. More...
AccessionPRJNA290300; dbGaP: phs000958
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 20-Jul-2015
NHGRI
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments100
Other datasets
BioSample200
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases12,195
Data volume, Tbytes4.94
Homo sapiens encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA290301Homo sapiensCSER: The MedSeq Project (BRIGHAM AND WOMEN'S HOSPITAL)

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