A classification model for distinguishing copy number variants from cancer-related alterations (Q33594892)

28 July 2017

title

A classification model for distinguishing copy number variants from cancer-related alterations (English)

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28 July 2017

1

Irina Ostrovnaya

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28 July 2017

Gouri Nanjangud

2

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28 July 2017

Adam B Olshen

series ordinal

3

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28 July 2017

language of work or name

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2 June 2010

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28 July 2017

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28 July 2017

volume

11

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28 July 2017

page(s)

297

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Creative Commons Attribution 2.0 Generic

28 July 2017

copyright license

start time

2 June 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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April 2022 Public Data File from Crossref

cites work

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Copy number variation at 1q21.1 associated with neuroblastoma

14 July 2018

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Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer

14 July 2018

1 reference

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Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis

14 July 2018

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Comprehensive genomic characterization defines human glioblastoma genes and core pathways

14 July 2018

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Small deletion variants have stable breakpoints commonly associated with alu elements.

14 July 2018

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

14 July 2018

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Chromosomal breakpoints in primary colon cancer cluster at sites of structural variants in the genome

14 July 2018

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

14 July 2018

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Stochastic segmentation models for array-based comparative genomic hybridization data analysis

14 July 2018

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Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability

14 July 2018

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Challenges and standards in integrating surveys of structural variation

14 July 2018

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Methods and strategies for analyzing copy number variation using DNA microarrays

14 July 2018

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Strong association of de novo copy number mutations with autism

14 July 2018

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

14 July 2018

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14 July 2018

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Global variation in copy number in the human genome

14 July 2018

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High-resolution global genomic survey of 178 gliomas reveals novel regions of copy number alteration and allelic imbalances

14 July 2018

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Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

14 July 2018

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Copy number variation: new insights in genome diversity

14 July 2018

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IGHV gene insertions and deletions in chronic lymphocytic leukemia: "CLL-biased" deletions in a subset of cases with stereotyped receptors

14 July 2018

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Bias of selection on human copy-number variants

14 July 2018

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A comparison study: applying segmentation to array CGH data for downstream analyses

14 July 2018

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Segmental duplications and copy-number variation in the human genome

14 July 2018

1 reference

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2897829

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2897829

Detection of large-scale variation in the human genome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2897829

Regulation of immunoglobulin heavy-chain gene rearrangements

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2897829

By-products of immunoglobulin somatic hypermutation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2897829

Variation of CNV distribution in five different ethnic populations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2897829

30 October 2018

Identifiers

DOI

10.1186/1471-2105-11-297

1 reference

journals/bmcbi/OstrovnayaNO10

28 July 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

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28 July 2017

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