Quantitative analysis of single nucleotide polymorphisms within copy number variation (Q33394240)

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scientific article

Language	Label	Description	Also known as
English	Quantitative analysis of single nucleotide polymorphisms within copy number variation	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Quantitative analysis of single nucleotide polymorphisms within copy number variation (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

4

object named as

Charles R Cantor

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

author name string

Soohyun Lee

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Simon Kasif

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Zhiping Weng

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

language of work or name

0 references

publication date

18 December 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

e3906

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

copyright license

Creative Commons Attribution 4.0 International

18 December 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

A panel of ancestry informative markers for estimating individual biogeographical ancestry and admixture from four continents: utility and applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

The diploid genome sequence of an individual human

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Mendelian proportions in a mixed population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Germ-line DNA copy number variation frequencies in a large North American population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

A comprehensive analysis of common copy-number variations in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Global variation in copy number in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry in genomics research

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Primate segmental duplications: crucibles of evolution, diversity and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Bias of selection on human copy-number variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Segmental duplications and copy-number variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Fine-scale structural variation of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Detection of large-scale variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Detection of genotyping errors by Hardy-Weinberg equilibrium testing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Intense and highly localized gene conversion activity in human meiotic crossover hot spots

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Abundant gene conversion between arms of palindromes in human and ape Y chromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Population admixture: detection by Hardy-Weinberg test and its quantitative effects on linkage-disequilibrium methods for localizing genes underlying complex traits.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

A Bayesian characterization of Hardy-Weinberg disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Testing for homogeneity of Hardy-Weinberg disequilibrium using data sampled from several populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

A disequilibrium coefficient approach to Hardy-Weinberg testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2600609

21 June 2018

Common deletion polymorphisms in the human genome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003906

21 January 2018

A Comparison of Tests for Hardy-Weinberg Equilibrium

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003906

21 January 2018

Complex SNP-related sequence variation in segmental genome duplications

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003906

21 January 2018

Impact of Violations and Deviations in Hardy-Weinberg Equilibrium on Postulated Gene-Disease Associations

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0003906

21 January 2018

Quantification of the power of Hardy-Weinberg equilibrium testing to detect genotyping error

1 reference

https://pubmed.ncbi.nlm.nih.gov/19093001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/19093001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0003906

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

2008PLoSO...3.3906L

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

0 references

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