Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data (Q30578002)

29 September 2017

Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data (English)

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29 September 2017

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Soon-Young Kim

1

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29 September 2017

Ji-Hong Kim

series ordinal

2

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29 September 2017

Yeun-Jun Chung

series ordinal

3

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29 September 2017

28 September 2012

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29 September 2017

Genomics & Informatics

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29 September 2017

10

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29 September 2017

194-199

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29 September 2017

3

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Creative Commons Attribution-NonCommercial 3.0 Unported

29 September 2017

start time

1 January 2012

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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

20 June 2018

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Copy number variations in East-Asian population and their evolutionary and functional implications

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The pitfalls of platform comparison: DNA copy number array technologies assessed

20 June 2018

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Comparing CNV detection methods for SNP arrays

20 June 2018

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Comparison of comparative genomic hybridization technologies across microarray platforms

20 June 2018

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A robust statistical method for case-control association testing with copy number variation

20 June 2018

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

20 June 2018

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Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors

20 June 2018

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Mapping and sequencing of structural variation from eight human genomes

20 June 2018

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

20 June 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

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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Structural variation in the human genome

20 June 2018

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

20 June 2018

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Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

20 June 2018

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A genome-wide CNV association study on panic disorder in a Japanese population.

26 November 2018

1 reference

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The potential role of VPREB1 gene copy number variation in susceptibility to rheumatoid arthritis.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3492655

26 November 2018

Identifiers

DOI

10.5808/GI.2012.10.3.194

1 reference

release_776ix2vuo5d3pnyw4kordoacvu

29 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/776ix2vuo5d3pnyw4kordoacvu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

29 September 2017

1 reference