(Q40844290)

24 September 2017

Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays (English)

1 reference

24 September 2017

Derek A Oldridge

1

1 reference

24 September 2017

Samprit Banerjee

2

1 reference

24 September 2017

Sunita R Setlur

3

1 reference

24 September 2017

Andrea Sboner

4

1 reference

24 September 2017

Francesca Demichelis

5

1 reference

24 September 2017

15 February 2010

1 reference

24 September 2017

Nucleic Acids Research

1 reference

24 September 2017

38

1 reference

24 September 2017

10

1 reference

24 September 2017

3275-3286

1 reference

Creative Commons Attribution-NonCommercial 2.5 Generic

24 September 2017

start time

10 May 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Copy number variants (CNVs) in primate species using array-based comparative genomic hybridization.

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

The evolutionary significance of copy number variation in the human genome

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Population analysis of large copy number variants and hotspots of human genetic disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Distinct genomic aberrations associated with ERG rearranged prostate cancer

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

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

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

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

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

SNP panel identification assay (SPIA): a genetic-based assay for the identification of cell lines

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

The fine-scale and complex architecture of human copy-number variation

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Characterizing the cancer genome in lung adenocarcinoma

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

A comparison of DNA copy number profiling platforms

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Copy-number variation and association studies of human disease

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Methods and strategies for analyzing copy number variation using DNA microarrays

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Principal components analysis corrects for stratification in genome-wide association studies

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Hotspots for copy number variation in chimpanzees and humans

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

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

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Detection of large-scale variation in the human genome

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Large-scale copy number polymorphism in the human genome

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

High-resolution global profiling of genomic alterations with long oligonucleotide microarray

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

The International HapMap Project

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

Estimation of the inbreeding coefficient through use of genomic data

24 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2879534

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

24 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKQ073

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKQ073

21 January 2018

Identifiers

DOI

10.1093/NAR/GKQ073

1 reference

release_7fun2iavvzgb7cclp6xzyxko2e

24 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/7fun2iavvzgb7cclp6xzyxko2e

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

24 September 2017

1 reference