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Accession: PRJNA291358 ID: 291358

Homo sapiens (human)

Homo sapiens Genome sequencing and assembly

See Genome Information for Homo sapiens
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66643 additional projects are related by organism.
Somatic mutations play a role in human neurological diseases as well as cancer. More...
AccessionPRJNA291358
Data TypeGenome sequencing and assembly
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Grants
  • "Training in the Molecular Biology of Neurodegeneration" (Grant ID T32 AG000222, NIH National Institute on Aging)
  • "Cell Identity Determination In Cerebral Cortex" (Grant ID R01 NS032457, NIH National Institute of Neurological Disorders and Stroke)
  • "Somatic mutations in epilepsy: whole genome sequence analysis of single neurons" (Grant ID R01 NS079277, NIH National Institute of Neurological Disorders and Stroke)
  • "Neuropsychiatric Genome-Scale and RDOC Individualized Domains (N-GRID)" (Grant ID P50 MH106933, NIH National Institute of Mental Health)
  • "Somatic Mutations in Autism Spectrum Disorder" (Grant ID U01 MH106883, NIH National Institute of Mental Health)
  • "Cellular and Developmental Biology" (Grant ID T32 GM007226, NIH National Institute of General Medical Sciences)
  • "Medical Scientists Training Program" (Grant ID T32 GM007753, NIH National Institute of General Medical Sciences)
SubmissionRegistration date: 29-Jul-2015
Children's Hospital Boston / Harvard Medical School
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments58
Other datasets
BioSample58
SRA Data Details
ParameterValue
Data volume, Gbases3,923
Data volume, Tbytes1.45

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