Systematic assessment of copy number variant detection via genome-wide SNP genotyping (Q37381957)

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scientific article published on 07 September 2008

Language	Label	Description	Also known as
English	Systematic assessment of copy number variant detection via genome-wide SNP genotyping	scientific article published on 07 September 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1 reference

based on heuristic

inferred from title

Jeffrey M. Kidd

3

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Deborah A Nickerson

5

object named as

Deborah A Nickerson

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Evan E. Eichler

4

object named as

Evan E Eichler

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

2

object named as

Troy Zerr

1 reference

Europe PubMed Central

20 August 2017

PMC publication ID

author name string

Gregory M Cooper

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

7 September 2008

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Nature Genetics

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

40

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Europe PubMed Central

PMC publication ID

20 August 2017

10

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

1199-1203

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Mapping and sequencing of structural variation from eight human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Paired-end mapping reveals extensive structural 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=2759751

6 September 2017

Diet and the evolution of human amylase gene copy number variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Mutational and selective effects on 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=2759751

6 September 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Completing the map of human genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Unsupervised segmentation of continuous genomic data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

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=2759751

6 September 2017

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=2759751

6 September 2017

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Discovery of previously unidentified genomic disorders from the duplication architecture 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=2759751

6 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions 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=2759751

6 September 2017

A haplotype map 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=2759751

6 September 2017

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=2759751

6 September 2017

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=2759751

6 September 2017

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

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=2759751

6 September 2017

alpha-Synuclein locus triplication causes Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

Molecular mechanisms for constitutional chromosomal rearrangements in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

6 September 2017

High-throughput genotyping of intermediate-size structural variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2759751

14 September 2017

Common deletion polymorphisms 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=2759751

2 September 2018

A worldwide survey of haplotype variation and linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG.236

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG.236

21 January 2018

Estimating the Dimension of a Model

1 reference

https://api.crossref.org/works/10.1038%2FNG.236

21 January 2018

Shotgun sequence assembly and recent segmental duplications within the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18776910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high-resolution survey of deletion polymorphism in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18776910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemical characterization of element 112

1 reference

https://api.crossref.org/works/10.1038%2FNG.236

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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