(Q33786964)

29 July 2017

title

The effect of algorithms on copy number variant detection (English)

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29 July 2017

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Debby W Tsuang

1

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author name string

Steven P Millard

2

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29 July 2017

Benjamin Ely

3

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29 July 2017

Peter Chi

4

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29 July 2017

Kenneth Wang

5

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29 July 2017

Wendy H Raskind

6

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29 July 2017

Sulgi Kim

7

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29 July 2017

Zoran Brkanac

8

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29 July 2017

Chang-En Yu

9

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29 July 2017

language of work or name

English

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publication date

30 December 2010

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29 July 2017

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29 July 2017

volume

5

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29 July 2017

issue

12

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29 July 2017

page(s)

e14456

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Creative Commons CC0 License

29 July 2017

copyright license

start time

30 December 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

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cites work

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The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci

4 July 2018

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Comparing CNV detection methods for SNP arrays

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012691

The HapMap and genome-wide association studies in diagnosis and therapy

4 July 2018

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Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012691

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

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012691

Extending genome-wide association studies to copy-number variation

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012691

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

4 July 2018

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

4 July 2018

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Large recurrent microdeletions associated with schizophrenia

4 July 2018

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Rare chromosomal deletions and duplications increase risk of schizophrenia

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012691

Strong association of de novo copy number mutations with sporadic schizophrenia

4 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3012691

Mapping and sequencing of structural variation from eight human genomes

4 July 2018

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

4 July 2018

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

4 July 2018

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

4 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

4 July 2018

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Methods and strategies for analyzing copy number variation using DNA microarrays

4 July 2018

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Completing the map of human genetic variation

4 July 2018

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Unsupervised segmentation of continuous genomic data

4 July 2018

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

4 July 2018

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Mapping autism risk loci using genetic linkage and chromosomal rearrangements

4 July 2018

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Global variation in copy number in the human genome

4 July 2018

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The Consortium on the Genetics of Endophenotypes in Schizophrenia: model recruitment, assessment, and endophenotyping methods for a multisite collaboration

4 July 2018

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Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes

4 July 2018

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4 July 2018

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Impact of sample selection on APOE epsilon 4 allele frequency: a comparison of two Alzheimer's disease samples.

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0014456

10.1371/JOURNAL.PONE.0014456

21 January 2018

Identifiers

DOI

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29 July 2017

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29 July 2017

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