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Haojing Shao

Researcher at University of Queensland

Publications -  17
Citations -  17133

Haojing Shao is an academic researcher from University of Queensland. The author has contributed to research in topics: Genome & Reference genome. The author has an hindex of 11, co-authored 17 publications receiving 11859 citations. Previous affiliations of Haojing Shao include Beijing Institute of Genomics & South China University of Technology.

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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

Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences

TL;DR: A calibrated phylogenetic tree is constructed on the basis of binary single-nucleotide variants and the more complex variants onto it, estimating the number of mutations for each class and shows bursts of extreme expansion in male numbers that have occurred independently among the five continental superpopulations examined.
Journal ArticleDOI

A large-scale screen for coding variants predisposing to psoriasis.

TL;DR: Single-variant and gene-based association analyses of nonsynonymous SNVs did not identify newly associated genes for psoriasis in the regions subjected to targeted resequencing, which suggests that coding variants in the 1,326 targeted genes contribute only a limited fraction of the overall genetic risk for Psoriasis.