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Kamen Radew

Researcher at University of Warsaw

Publications -  4
Citations -  15954

Kamen Radew is an academic researcher from University of Warsaw. The author has contributed to research in topics: Human genetic variation & Genome-wide association study. The author has an hindex of 3, co-authored 4 publications receiving 10817 citations.

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Journal ArticleDOI

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

An integrated 3-Dimensional Genome Modeling Engine for data-driven simulation of spatial genome organization.

TL;DR: 3D-GNOME (3-Dimensional Genome Modeling Engine), a complete computational pipeline for 3D simulation using ChIA-PET data, is reported, demonstrating the effectiveness of 3D- GNOME in building 3D genome models at multiple levels, including the entire genome, individual chromosomes, and specific segments at megabase and kilobase resolution.

An integrated map of structural variation in 2,504 human genomes_supplement

Sudmant Ph, +494 more
TL;DR: An integrated set of eight structural variant classes comprising both balanced and unbalanced variants, which are constructed using short-read DNA sequencing data and statistically phased onto haplotype blocks in 26 human populations are described.