CONAN: copy number variation analysis software for genome-wide association studies - Wikidata - awgldk - TriplyDB

CONAN: copy number variation analysis software for genome-wide association studies

CONAN: copy number variation analysis software for genome-wide association studies

http://www.wikidata.org/entity/Q33603606

about

Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data DEAR1 is a chromosome 1p35 tumor suppressor and master regulator of TGF-β-driven epithelial-mesenchymal transition Detection of genome-wide copy number variations in two chicken lines divergently selected for abdominal fat content.Beyond missing heritability: prediction of complex traits HD-CNV: hotspot detector for copy number variants.Genome wide analysis reveals single nucleotide polymorphisms associated with fatness and putative novel copy number variants in three pig breeds.Improving genetic risk prediction by leveraging pleiotropy.ParseCNV integrative copy number variation association software with quality tracking.A comparison of genomic copy number calls by Partek Genomics Suite, Genotyping Console and Birdsuite algorithms to quantitative PCR SMYD5 Controls Heterochromatin and Chromosome Integrity during Embryonic Stem Cell Differentiation.

P2860

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P2860

CONAN: copy number variation analysis software for genome-wide association studies

http://www.wikidata.org/entity/Q33603606

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

CONAN: copy number variation analysis software for genome-wide association studies

@ast

CONAN: copy number variation analysis software for genome-wide association studies

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type

label

CONAN: copy number variation analysis software for genome-wide association studies

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CONAN: copy number variation analysis software for genome-wide association studies

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prefLabel

CONAN: copy number variation analysis software for genome-wide association studies

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CONAN: copy number variation analysis software for genome-wide association studies

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BMC Bioinformatics

P1476

CONAN: copy number variation analysis software for genome-wide association studies

@en

P2093

Anita Kloss-Brandstätter

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Florian Haider

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Günther Specht

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Hansi Weissensteiner

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Heinz-Erich Wichmann

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Sebastian Schönherr

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Thomas Kluckner

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P2860

Genome-wide QTL mapping for three traits related to teat number in a White Duroc x Erhualian pig resource population.

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

The complete genome of an individual by massively parallel DNA sequencing

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

Global variation in copy number in the human genome

The human genome browser at UCSC

PLINK: a tool set for whole-genome association and population-based linkage analyses

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

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

P2888

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318

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10.1186/1471-2105-11-318

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11

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Christian Gieger

Florian Kronenberg

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44671779

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genome-wide association study

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2894823

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