Hochschulschrift

Strategies for Genome-Wide Association Analyses of Raw Copy Number Variation Data

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Alternative title: Strategien für genom-weite Assoziations-Analysen von Rohdaten für Kopienzahl Variationen (CNVs)

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: Marburg, Philipps-Universität Marburg, Diss., 2013

Keyword: Genetik
Fettsucht
Aufmerksamkeits-Defizit-Syndrom
Augenheilkunde
Augenkrankheit

Event: Veröffentlichung

(where): Marburg

(who): Philipps-Universität Marburg

(when): 2013

Creator: Jarick, Ivonne

Contributor: Schäfer, Helmut

URN: urn:nbn:de:hebis:04-z2013-07327

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 25.03.2025, 1:42 PM CET

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Hochschulschrift

Associated

Jarick, Ivonne
Schäfer, Helmut
Philipps-Universität Marburg

Time of origin

2013

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Strategies for genome-wide association analyses of raw copy number variation data

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Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

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Strategies for Genome-Wide Association Analyses of Raw Copy Number Variation Data

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Other Objects (12)

Strategies for genome-wide association analyses of raw copy number variation data

Genome-wide analyses of stallion fertility

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

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Integrative bioinformatics analyses of genome-wide RNAi screens

Genome-wide analyses of complex traits in the horse

Genome-wide proteomics and quantitative analyses on halophilic archaea

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder

Strategies for genome-wide association analyses of raw copy number variation data

Genome-wide analyses of stallion fertility

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Integrative bioinformatics analyses of genome-wide RNAi screens

Integrative bioinformatics analyses of genome-wide RNAi screens

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Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder

Strategies for genome-wide association analyses of raw copy number variation data

Genome-wide analyses of stallion fertility

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Integrative bioinformatics analyses of genome-wide RNAi screens

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Genome-wide analyses of complex traits in the horse

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Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder

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