(Q34310095)

1 August 2017

title

Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies (English)

1 reference

1 August 2017

6

Mads Melbye

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Bjarke Feenstra

object named as

Bjarke Feenstra

5

0 references

Eleanor Feingold

object named as

Eleanor Feingold

9

0 references

Mary L. Marazita

8

object named as

Mary L Marazita

1 reference

1 August 2017

3

Caitlin P McHugh

1 reference

1 August 2017

Xiaojing Zheng

1

1 reference

1 August 2017

John R Shaffer

2

1 reference

1 August 2017

Cathy C Laurie

4

1 reference

1 August 2017

Jeffrey C Murray

7

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1 August 2017

publication date

1 April 2012

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1 August 2017

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1 August 2017

volume

36

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1 August 2017

issue

3

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1 August 2017

page(s)

253-262

1 reference

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Statistical issues in the analysis of DNA Copy Number Variations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Integrated study of copy number states and genotype calls using high-density SNP arrays

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Genome instability, cancer and aging

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping 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=3696390

The NCBI dbGaP database of genotypes and phenotypes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Methods and strategies for analyzing copy number variation using DNA microarrays

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH 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=3696390

The Danish National Birth Cohort - its background, structure and aim

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.21618

The Danish National Birth Cohort--its background, structure and aim.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3696390

Somatic mutations are frequent and increase with age in human kidney epithelial cells

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22714937

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.21618

1 reference

1 August 2017

1 reference

1 August 2017

1 reference