(Q33511862)

27 July 2017

title

An optimization framework for unsupervised identification of rare copy number variation from SNP array data (English)

1 reference

27 July 2017

Mehmet Koyutürk

2

0 references

author name string

Gökhan Yavas

1

1 reference

27 July 2017

Meral Ozsoyoğlu

3

1 reference

27 July 2017

Meetha P Gould

4

1 reference

27 July 2017

Thomas LaFramboise

5

1 reference

27 July 2017

publication date

23 October 2009

1 reference

27 July 2017

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27 July 2017

volume

10

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27 July 2017

issue

10

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27 July 2017

page(s)

R119

1 reference

https://scigraph.springernature.com/pub.10.1186/gb-2009-10-10-r119

27 July 2017

exact match

0 references

cites work

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

21 June 2018

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

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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Optimization by Simulated Annealing

21 June 2018

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Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation

21 June 2018

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Strong association of de novo copy number mutations with autism

21 June 2018

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

21 June 2018

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A faster circular binary segmentation algorithm for the analysis of array CGH data

21 June 2018

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A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

21 June 2018

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21 June 2018

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21 June 2018

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Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays

21 June 2018

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21 June 2018

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

21 June 2018

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A haplotype map of the human genome

21 June 2018

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Homozygous deletions and chromosome amplifications in human lung carcinomas revealed by single nucleotide polymorphism array analysis

21 June 2018

1 reference

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

21 June 2018

1 reference

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

21 June 2018

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

21 June 2018

1 reference

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dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

21 June 2018

1 reference

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A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2784334

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2784334

Model-based analysis of oligonucleotide arrays: expression index computation and outlier detection

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2784334

A genome-wide scalable SNP genotyping assay using microarray technology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2784334

Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19849861

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GB-2009-10-10-R119

1 reference

Dimensions Publication ID

27 July 2017

0 references

1 reference

27 July 2017

1 reference