(Q35079853)

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Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data

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scholarly article

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Europe PubMed Central

PubMed publication ID

6 August 2017

Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

Marylyn D. Ritchie

7

object named as

Marylyn D Ritchie

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Europe PubMed Central

PubMed publication ID

6 August 2017

Sarah Pendergrass

5

object named as

Sarah A Pendergrass

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Europe PubMed Central

PubMed publication ID

6 August 2017

author name string

Carrie B Moore

1

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Europe PubMed Central

PubMed publication ID

6 August 2017

John R Wallace

2

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Europe PubMed Central

PubMed publication ID

6 August 2017

Daniel J Wolfe

3

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Europe PubMed Central

PubMed publication ID

6 August 2017

Alex T Frase

4

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Europe PubMed Central

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6 August 2017

Kenneth M Weiss

6

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Europe PubMed Central

PubMed publication ID

6 August 2017

publication date

26 December 2013

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Europe PubMed Central

PubMed publication ID

6 August 2017

9

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Europe PubMed Central

PubMed publication ID

6 August 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

e1003959

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Europe PubMed Central

PubMed publication ID

6 August 2017

copyright license

Creative Commons Attribution 4.0 International

26 December 2013

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April 2022 Public Data File from Crossref

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0 references

Using BioBin to explore rare variant population stratification

1 reference

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The timing of pigmentation lightening in Europeans

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Limitations of the human reference genome for personalized genomics

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

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Effect of population stratification analysis on false-positive rates for common and rare variants

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Variation in the mutation rate across mammalian genomes

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Synthetic associations created by rare variants do not explain most GWAS results

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8 July 2018

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8 July 2018

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8 July 2018

Inference of unexpected genetic relatedness among individuals in HapMap Phase III.

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8 July 2018

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

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8 July 2018

New approaches to population stratification in genome-wide association studies

1 reference

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8 July 2018

Characterization of missing human genome sequences and copy-number polymorphic insertions

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8 July 2018

A method and server for predicting damaging missense mutations

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8 July 2018

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8 July 2018

Building the sequence map of the human pan-genome

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Genetic variation and recent positive selection in worldwide human populations: evidence from nearly 1 million SNPs

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Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

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8 July 2018

Measuring the rates of spontaneous mutation from deep and large-scale polymorphism data

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8 July 2018

Discovery of rare variants via sequencing: implications for the design of complex trait association studies

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8 July 2018

Signals of recent positive selection in a worldwide sample of human populations

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8 July 2018

A groupwise association test for rare mutations using a weighted sum statistic

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Natural selection has driven population differentiation in modern humans

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8 July 2018

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8 July 2018

A map of recent positive selection in the human genome

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SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans

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8 July 2018

Mutation rate variation in the mammalian genome

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8 July 2018

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27 September 2018

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12 December 2020

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10.1371/JOURNAL.PGEN.1003959

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Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

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Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

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6 August 2017

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