(Q34085504)

30 July 2017

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

1 reference

30 July 2017

1 reference

7

Michiaki Kubo

1 reference

30 July 2017

5

Atsushi Takahashi

1 reference

30 July 2017

6

Yusuke Nakamura

1 reference

30 July 2017

3

Naoya Hosono

1 reference

30 July 2017

1

Natsuhiko Kumasaka

1 reference

30 July 2017

8

Naoyuki Kamatani

1 reference

30 July 2017

Hironori Fujisawa

2

1 reference

PubMed ID

22125222

30 July 2017

Yukinori Okada

series ordinal

4

1 reference

30 July 2017

1 December 2011

1 reference

30 July 2017

1 reference

30 July 2017

35

1 reference

30 July 2017

8

1 reference

30 July 2017

831-844

1 reference

Basic local alignment search tool

30 July 2017

1 reference

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

Determination of cytochrome P450 2D6 (CYP2D6) gene copy number by real-time quantitative PCR.

21 January 2018

1 reference

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

A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

21 January 2018

1 reference

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

cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Origins and functional impact of copy number variation in the human genome

21 January 2018

1 reference

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

Genomic control for association studies

21 January 2018

1 reference

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

Structural variation in the human genome

21 January 2018

1 reference

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

Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays

21 January 2018

1 reference

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

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

21 January 2018

1 reference

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

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

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

Genome-wide association study of hematological and biochemical traits in a Japanese population

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Finding the missing heritability of complex diseases

21 January 2018

1 reference

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

BioHMM: a heterogeneous hidden Markov model for segmenting array CGH data

21 January 2018

1 reference

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

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

21 January 2018

1 reference

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

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

21 January 2018

1 reference

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

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

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

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

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

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Sparse representation and Bayesian detection of genome copy number alterations from microarray data

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Global variation in copy number in the human genome

21 January 2018

1 reference

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

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

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

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

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

Bayesian methods for examining Hardy-Weinberg equilibrium

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Hidden Markov models approach to the analysis of array CGH data

21 January 2018

1 reference

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

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

1 reference

30 July 2017

1 reference

PubMed ID

22125222