(Q33797878)

29 July 2017

title

Accuracy of CNV Detection from GWAS Data (English)

1 reference

genome-wide association study

29 July 2017

main subject

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Dandan Zhang

1

0 references

Chunyu Liu

object named as

Chunyu Liu

8

0 references

Elliot S Gershon

7

object named as

Elliot S Gershon

1 reference

29 July 2017

Yudong Qian

2

1 reference

29 July 2017

Nirmala Akula

3

1 reference

29 July 2017

Ney Alliey-Rodriguez

4

1 reference

29 July 2017

Jinsong Tang

5

1 reference

29 July 2017

Bipolar Genome Study

6

1 reference

29 July 2017

language of work or name

English

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publication date

13 January 2011

1 reference

29 July 2017

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29 July 2017

volume

6

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29 July 2017

issue

1

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29 July 2017

page(s)

e14511

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Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

13 January 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Identification of recurrent regions of Copy-Number Variants across multiple individuals

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Comparing CNV detection methods for SNP arrays

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Genome-wide association study of bipolar disorder in European American and African American individuals

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Copy number variants, diseases and gene expression

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Singleton deletions throughout the genome increase risk of bipolar disorder

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Large recurrent microdeletions associated with schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Mapping and sequencing of structural variation from eight human genomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Genotype, haplotype and copy-number variation in worldwide human populations

28 July 2018

1 reference

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

28 July 2018

1 reference

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Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

28 July 2018

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

28 July 2018

1 reference

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Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

28 July 2018

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PLINK: a tool set for whole-genome association and population-based linkage analyses

28 July 2018

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Strong association of de novo copy number mutations with autism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

28 July 2018

1 reference

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Global variation in copy number in the human genome

28 July 2018

1 reference

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STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments

28 July 2018

1 reference

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

28 July 2018

1 reference

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Whole genome DNA copy number changes identified by high density oligonucleotide arrays

28 July 2018

1 reference

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

28 July 2018

1 reference

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Detection of large-scale variation in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Large-scale copy number polymorphism in the human genome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3020939

Rare chromosomal deletions and duplications increase risk of schizophrenia

28 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0014511

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0014511

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

21 January 2018

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

21 January 2018

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Impact of normalization on miRNA microarray expression profiling

21 January 2018

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10.1371/JOURNAL.PONE.0014511

21 January 2018

Identifiers

DOI

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29 July 2017

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29 July 2017

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