PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data (Q34085504)

30 July 2017

title

PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data (English)

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30 July 2017

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7

Michiaki Kubo

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5

Atsushi Takahashi

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6

Yusuke Nakamura

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3

Naoya Hosono

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1

Natsuhiko Kumasaka

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8

Naoyuki Kamatani

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30 July 2017

Hironori Fujisawa

2

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30 July 2017

Yukinori Okada

series ordinal

4

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30 July 2017

publication date

1 December 2011

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30 July 2017

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30 July 2017

volume

35

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30 July 2017

issue

8

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30 July 2017

page(s)

831-844

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Basic local alignment search tool

30 July 2017

cites work

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

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21 January 2018

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

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A method to address differential bias in genotyping in large-scale association studies

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21 January 2018

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A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

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Bayesian methods for examining Hardy-Weinberg equilibrium

21 January 2018

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PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

21 January 2018

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Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

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Hidden Markov models approach to the analysis of array CGH data

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20633

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GEPI.20633

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30 July 2017

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