Markov Models for inferring copy number variations from genotype data on Illumina platforms - Wikidata - awgldk - TriplyDB

Markov Models for inferring copy number variations from genotype data on Illumina platforms

Markov Models for inferring copy number variations from genotype data on Illumina platforms

http://www.wikidata.org/entity/Q33425649

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Reconstructing DNA copy number by joint segmentation of multiple sequences RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION.A method for calling copy number polymorphism using haplotypes.Statistical issues in the analysis of DNA Copy Number Variations.VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions.Detection and interpretation of genomic structural variation in health and disease.Frequency of KLK3 gene deletions in the general population.An integrative segmentation method for detecting germline copy number variations in SNP arrays.

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Markov Models for inferring copy number variations from genotype data on Illumina platforms

http://www.wikidata.org/entity/Q33425649

description

2009 nî lūn-bûn

@nan

2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

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2009年论文

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name

Markov Models for inferring co ...... ype data on Illumina platforms

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Markov Models for inferring co ...... ype data on Illumina platforms

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type

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Markov Models for inferring co ...... ype data on Illumina platforms

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Markov Models for inferring co ...... ype data on Illumina platforms

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Markov Models for inferring co ...... ype data on Illumina platforms

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Markov Models for inferring co ...... ype data on Illumina platforms

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Markov Models for inferring co ...... ype data on Illumina platforms

@en

P2093

Chiara Sabatti

http://www.w3.org/2001/XMLSchema#string

Hui Wang

http://www.w3.org/2001/XMLSchema#string

Hylke Blauw

http://www.w3.org/2001/XMLSchema#string

Roel A Ophoff

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P2860

Large recurrent microdeletions associated with schizophrenia

Global variation in copy number in the human genome

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

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

Inferring the location and effect of tumor suppressor genes by instability-selection modeling of allelic-loss data.

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

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

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1-22

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scholarly article

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10.1159/000210445

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1

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68

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Leonard H van den Berg

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2009-04-01T00:00:00Z

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24251462

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19339782

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2880724

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