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Iain Mathieson

Researcher at University of Pennsylvania

Publications -  96
Citations -  24763

Iain Mathieson is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Population & Selection (genetic algorithm). The author has an hindex of 28, co-authored 83 publications receiving 17508 citations. Previous affiliations of Iain Mathieson include University of Oxford & Wellcome Trust Centre for Human Genetics.

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A global reference for human genetic variation.

Adam Auton, +517 more
- 01 Oct 2015 - 
TL;DR: The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and has reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-generation sequencing, deep exome sequencing, and dense microarray genotyping.

A global reference for human genetic variation

Adam Auton, +479 more
TL;DR: The 1000 Genomes Project as mentioned in this paper provided a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations, and reported the completion of the project, having reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole genome sequencing, deep exome sequencing and dense microarray genotyping.
Journal ArticleDOI

The Simons Genome Diversity Project: 300 genomes from 142 diverse populations

Swapan Mallick, +104 more
- 13 Oct 2016 - 
TL;DR: It is demonstrated that indigenous Australians, New Guineans and Andamanese do not derive substantial ancestry from an early dispersal of modern humans; instead, their modern human ancestry is consistent with coming from the same source as that of other non-Africans.
Journal ArticleDOI

Genome-wide patterns of selection in 230 ancient Eurasians

TL;DR: A genome-wide scan for selection using ancient DNA is reported, capitalizing on the largest ancient DNA data set yet assembled: 230 West Eurasians who lived between 6500 and 300 bc, including 163 with newly reported data.
Journal ArticleDOI

Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

TL;DR: The performance of Platypus is demonstrated by comparing with SAMtools and GATK on whole-genome and exome-capture data, by identifying de novo variation in 15 parent-offspring trios with high sensitivity and specificity, and by estimating human leukocyte antigen genotypes directly from variant calls.