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Accession: PRJNA360454 ID: 360454

Homo sapiens (human)

Homo Sapien Variation Detection via Hybrid Sequencing Data

See Genome Information for Homo sapiens
We developed a hybrid structural variant assembly (HySA) approach that integrates sequencing reads from next-generation sequencing and single-molecule sequencing technologies to accurately assemble and detect structural variations in human genomes. More...
AccessionPRJNA360454
Data TypeVariation
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Grants
  • "An Integrative Analysis of Structural Variation for the 1000 Genomes Project" (Grant ID U41 HG007497, National Human Genome Research Institute)
  • "Cancer Center Support (CORE) Grant" (Grant ID P30 CA016672, National Cancer Institute)
  • "Applying the Cloud Computing resources to efficiently and comprehensively accomplish genomic analysis of TCGA/ICGC samples" (Grant ID R01 CA172652, National Cancer Institute)
SubmissionRegistration date: 6-Jan-2017
MD Anderson Cancer Center
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Variation (dbVar)22645

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    Homo Sapien Variation Detection via Hybrid Sequencing Data
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