(Q34237589)

31 July 2017

title

Low-pass genome-wide sequencing and variant inference using identity-by-descent in an isolated human population (English)

1 reference

31 July 2017

A Gusev

1

1 reference

31 July 2017

M J Shah

2

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31 July 2017

E E Kenny

3

1 reference

31 July 2017

A Ramachandran

4

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31 July 2017

J K Lowe

5

1 reference

31 July 2017

J Salit

6

1 reference

31 July 2017

C C Lee

7

1 reference

31 July 2017

E C Levandowsky

8

1 reference

31 July 2017

T N Weaver

9

1 reference

31 July 2017

Q C Doan

10

1 reference

31 July 2017

H E Peckham

11

1 reference

31 July 2017

S F McLaughlin

12

1 reference

31 July 2017

M R Lyons

13

1 reference

31 July 2017

V N Sheth

14

1 reference

31 July 2017

M Stoffel

15

1 reference

31 July 2017

F M De La Vega

16

1 reference

31 July 2017

J M Friedman

17

1 reference

31 July 2017

J L Breslow

18

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31 July 2017

I Pe'er

19

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31 July 2017

language of work or name

English

0 references

publication date

30 November 2011

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31 July 2017

number of pages

11

1 reference

based on heuristic

inferred from page(s)

published in

Genetics

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31 July 2017

volume

190

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31 July 2017

issue

2

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31 July 2017

page(s)

679-689

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Low-coverage sequencing: implications for design of complex trait association studies

31 July 2017

cites work

1 reference

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Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population

6 July 2018

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A map of human genome variation from population-scale sequencing

6 July 2018

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Dindel: accurate indel calls from short-read data

6 July 2018

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Reconciling the analysis of IBD and IBS in complex trait studies

6 July 2018

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genotype imputation for genome-wide association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

High-resolution detection of identity by descent in unrelated individuals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Accurate detection and genotyping of SNPs utilizing population sequencing data

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Population genetic inference from genomic sequence variation

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

A SNP discovery method to assess variant allele probability from next-generation resequencing data

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Exome sequencing identifies the cause of a mendelian disorder

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

6 July 2018

1 reference

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Targeted capture and massively parallel sequencing of 12 human exomes

6 July 2018

1 reference

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Recurring mutations found by sequencing an acute myeloid leukemia genome

6 July 2018

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A highly annotated whole-genome sequence of a Korean individual

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Massively parallel exon capture and library-free resequencing across 16 genomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genotype-imputation accuracy across worldwide human populations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

GOrilla: a tool for discovery and visualization of enriched GO terms in ranked gene lists

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

The diploid genome sequence of an Asian individual

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Accurate whole human genome sequencing using reversible terminator chemistry

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Whole population, genome-wide mapping of hidden relatedness

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Next-generation DNA sequencing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

The complete genome of an individual by massively parallel DNA sequencing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

The diploid genome sequence of an individual human

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

A new multipoint method for genome-wide association studies by imputation of genotypes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Genome-wide association studies for common diseases and complex traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Linkage disequilibrium in humans: models and data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Use of population isolates for mapping complex traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Initial sequencing and analysis of the human genome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3276614

Are common disease susceptibility alleles the same in outbred and founder populations?

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22135348

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1534/GENETICS.111.134874

1 reference

31 July 2017

1 reference

31 July 2017

1 reference