(Q34973122)

5 August 2017

title

RECONSTRUCTING DNA COPY NUMBER BY PENALIZED ESTIMATION AND IMPUTATION. (English)

1 reference

5 August 2017

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Zhongyang Zhang

1

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5 August 2017

Kenneth Lange

series ordinal

2

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5 August 2017

Roel Ophoff

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3

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5 August 2017

Chiara Sabatti

series ordinal

4

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5 August 2017

publication date

1 December 2010

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The Annals of Applied Statistics

5 August 2017

published in

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5 August 2017

volume

4

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5 August 2017

issue

4

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5 August 2017

page(s)

1749-1773

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maintained by WikiProject

5 August 2017

WikiProject Mathematics

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cites work

Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Recurrent CNVs disrupt three candidate genes in schizophrenia patients

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Large recurrent microdeletions associated with schizophrenia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Analysis of array CGH data for cancer studies using fused quantile regression

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Spatial smoothing and hot spot detection for CGH data using the fused lasso

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Global variation in copy number in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Detection of large-scale variation in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

Large-scale copy number polymorphism in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3092301

8 July 2018

Identifiers

DOI

10.1214/10-AOAS357

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release_ur7f6wtywrfura3uwpj6ke45ay

5 August 2017

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Fatcat

https://api.fatcat.wiki/v0/release/ur7f6wtywrfura3uwpj6ke45ay

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3092301

1 reference

5 August 2017

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