The Role of Constitutional Copy Number Variants in Breast Cancer. - Wikidata - awgldk - TriplyDB

The Role of Constitutional Copy Number Variants in Breast Cancer.

The Role of Constitutional Copy Number Variants in Breast Cancer.

http://www.wikidata.org/entity/Q37200793

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Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers.SNP Arrays.

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The Role of Constitutional Copy Number Variants in Breast Cancer.

http://www.wikidata.org/entity/Q37200793

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 08 September 2015

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

The Role of Constitutional Copy Number Variants in Breast Cancer.

@en

The Role of Constitutional Copy Number Variants in Breast Cancer.

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type

label

The Role of Constitutional Copy Number Variants in Breast Cancer.

@en

The Role of Constitutional Copy Number Variants in Breast Cancer.

@nl

prefLabel

The Role of Constitutional Copy Number Variants in Breast Cancer.

@en

The Role of Constitutional Copy Number Variants in Breast Cancer.

@nl

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MICROARRAYS4030407

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Microarrays (Basel, Switzerland)

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The Role of Constitutional Copy Number Variants in Breast Cancer.

@en

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George A R Wiggins

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John F Pearson

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Logan C Walker

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P2860

Mapping and sequencing of structural variation from eight human genomes

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Genome-wide association study identifies novel breast cancer susceptibility loci

Paired-end mapping reveals extensive structural variation in the human genome

Global variation in copy number in the human genome

SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data

Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays

A copy number variation map of the human genome

Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium

Origins and functional impact of copy number variation in the human genome

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407-423

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scholarly article

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10.3390/MICROARRAYS4030407

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4996380

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