CONAN: copy number variation analysis software for genome-wide association studies
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2105
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
CONAN: copy number variation analysis software for genome-wide association studies ; volume:11 ; number:1 ; day:14 ; month:6 ; year:2010 ; pages:1-9 ; date:12.2010
BMC bioinformatics ; 11, Heft 1 (14.6.2010), 1-9, 12.2010
- Urheber
-
Forer, Lukas
- Beteiligte Personen und Organisationen
-
Schönherr, Sebastian
Weissensteiner, Hansi
Haider, Florian
Kluckner, Thomas
Gieger, Christian
Wichmann, Heinz-Erich
Specht, Günther
Kronenberg, Florian
Kloss-Brandstätter, Anita
SpringerLink (Online service)
- DOI
-
10.1186/1471-2105-11-318
- URN
-
urn:nbn:de:1111-2016021720747
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:35 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Forer, Lukas
- Schönherr, Sebastian
- Weissensteiner, Hansi
- Haider, Florian
- Kluckner, Thomas
- Gieger, Christian
- Wichmann, Heinz-Erich
- Specht, Günther
- Kronenberg, Florian
- Kloss-Brandstätter, Anita
- SpringerLink (Online service)
Ähnliche Objekte (12)
Lipoprotein(a): from Causality to Treatment
Prediction of cardiovascular risk by Lp(a) concentrations or genetic variants within the LPA gene region
Human Genetics and the Causal Role of Lipoprotein(a) for Various Diseases
Plasmid-normalized quantification of relative mitochondrial DNA copy number
Genomweite Assoziationsstudien zu Adipositas und was wir daraus lernen
An optimized procedure for the design and evaluation of Ecotilling assays
Supporting the evidence for human trait-associated genetic variants by computational biology methods and multi-level data integration.
Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number
eCOMPAGT integrates mtDNA: import, validation and export of mitochondrial DNA profiles for population genetics, tumour dynamics and genotype-phenotype association studies
Evaluating the Causal Relation of ApoA-IV with Disease-Related Traits - A Bidirectional Two-sample Mendelian Randomization Study
Genome-wide copy number variations in Oryza sativa L
Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals
Lipoprotein(a): from Causality to Treatment
Prediction of cardiovascular risk by Lp(a) concentrations or genetic variants within the LPA gene region
Human Genetics and the Causal Role of Lipoprotein(a) for Various Diseases
Plasmid-normalized quantification of relative mitochondrial DNA copy number
Genomweite Assoziationsstudien zu Adipositas und was wir daraus lernen
An optimized procedure for the design and evaluation of Ecotilling assays
Supporting the evidence for human trait-associated genetic variants by computational biology methods and multi-level data integration.
Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number
eCOMPAGT integrates mtDNA: import, validation and export of mitochondrial DNA profiles for population genetics, tumour dynamics and genotype-phenotype association studies
Evaluating the Causal Relation of ApoA-IV with Disease-Related Traits - A Bidirectional Two-sample Mendelian Randomization Study
Genome-wide copy number variations in Oryza sativa L
Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals
Lipoprotein(a): from Causality to Treatment
Prediction of cardiovascular risk by Lp(a) concentrations or genetic variants within the LPA gene region
Human Genetics and the Causal Role of Lipoprotein(a) for Various Diseases
Plasmid-normalized quantification of relative mitochondrial DNA copy number
Genomweite Assoziationsstudien zu Adipositas und was wir daraus lernen
An optimized procedure for the design and evaluation of Ecotilling assays
Supporting the evidence for human trait-associated genetic variants by computational biology methods and multi-level data integration.
Nuclear and mitochondrial genetic variants associated with mitochondrial DNA copy number
eCOMPAGT integrates mtDNA: import, validation and export of mitochondrial DNA profiles for population genetics, tumour dynamics and genotype-phenotype association studies
Evaluating the Causal Relation of ApoA-IV with Disease-Related Traits - A Bidirectional Two-sample Mendelian Randomization Study
Genome-wide copy number variations in Oryza sativa L