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Jason P. Affourtit

Researcher at Hoffmann-La Roche

Publications -  32
Citations -  18509

Jason P. Affourtit is an academic researcher from Hoffmann-La Roche. The author has contributed to research in topics: Genome & Gene. The author has an hindex of 28, co-authored 32 publications receiving 16527 citations. Previous affiliations of Jason P. Affourtit include Life Technologies & Rensselaer Polytechnic Institute.

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A core gut microbiome in obese and lean twins

TL;DR: The faecal microbial communities of adult female monozygotic and dizygotic twin pairs concordant for leanness or obesity, and their mothers are characterized to address how host genotype, environmental exposure and host adiposity influence the gut microbiome.
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A Draft Sequence of the Neandertal Genome

TL;DR: The genomic data suggest that Neandertals mixed with modern human ancestors some 120,000 years ago, leaving traces of Ne andertal DNA in contemporary humans, suggesting that gene flow from Neand Bertals into the ancestors of non-Africans occurred before the divergence of Eurasian groups from each other.
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The genome of the domesticated apple ( Malus × domestica Borkh.)

Riccardo Velasco, +90 more
- 01 Oct 2010 - 
TL;DR: It is shown that a relatively recent (>50 million years ago) genome-wide duplication has resulted in the transition from nine ancestral chromosomes to 17 chromosomes in the Pyreae, which partly support the monophyly of the ancestral paleohexaploidy of eudicots.
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Paired-end mapping reveals extensive structural variation in the human genome.

TL;DR: High-throughput and massive paired-end mapping (PEM) was used to map SVs in an African and in a putatively European individual and identified shared and divergent SVs relative to the reference genome, documenting that the number of SVs among humans is much larger than initially hypothesized; many of the SVs potentially affect gene function.
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Mapping copy number variation by population-scale genome sequencing

Ryan E. Mills, +374 more
- 03 Feb 2011 - 
TL;DR: A map of unbalanced SVs is constructed based on whole genome DNA sequencing data from 185 human genomes, integrating evidence from complementary SV discovery approaches with extensive experimental validations, and serves as a resource for sequencing-based association studies.