(Q37593774)

21 August 2017

1 reference

title

Comparing CNV detection methods for SNP arrays (English)

1 reference

21 August 2017

Laura Winchester

1

1 reference

21 August 2017

Christopher Yau

series ordinal

2

1 reference

21 August 2017

Jiannis Ragoussis

series ordinal

3

1 reference

21 August 2017

publication date

8 September 2009

1 reference

Briefings in functional genomics & proteomics

21 August 2017

published in

1 reference

21 August 2017

volume

8

1 reference

21 August 2017

issue

5

1 reference

21 August 2017

page(s)

353-366

1 reference

Detection of large-scale variation in the human genome

21 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Fine-scale structural variation of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Paired-end mapping reveals extensive structural variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Large-scale genotyping of complex DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Copy-number variation and association studies of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

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/10.1093%2FBFGP%2FELP017

Unsupervised segmentation of continuous genomic data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

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/10.1093%2FBFGP%2FELP017

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/10.1093%2FBFGP%2FELP017

Modeling genetic inheritance of copy number variations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Major copy proportion analysis of tumor samples using SNP arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Circular binary segmentation for the analysis of array-based DNA copy number data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

A robust statistical method for case-control association testing with copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Challenges and standards in integrating surveys of structural variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Association study designs for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBFGP%2FELP017

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

COCI

https://opencitations.net/index/coci/api/v1/citations/10.1038/NG1696

30 October 2021

Identifiers

DOI

10.1093/BFGP/ELP017

1 reference

21 August 2017

0 references

1 reference