Rule-based induction method for haplotype comparison and identification of candidate disease loci
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1756-994X
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Rule-based induction method for haplotype comparison and identification of candidate disease loci ; volume:4 ; number:3 ; day:19 ; month:3 ; year:2012 ; pages:1-18 ; date:3.2012
Genome medicine ; 4, Heft 3 (19.3.2012), 1-18, 3.2012
- Creator
-
Karinen, Sirkku
- Contributor
-
Saarinen, Silva
Lehtonen, Rainer
Rastas, Pasi
Vahteristo, Pia
Aaltonen, Lauri A.
Hautaniemi, Sampsa
SpringerLink (Online service)
- DOI
-
10.1186/gm320
- URN
-
urn:nbn:de:1111-2016073129884
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:59 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Karinen, Sirkku
- Saarinen, Silva
- Lehtonen, Rainer
- Rastas, Pasi
- Vahteristo, Pia
- Aaltonen, Lauri A.
- Hautaniemi, Sampsa
- SpringerLink (Online service)
Other Objects (12)
Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes
On the use of haplotype phylogeny to detect disease susceptibility loci
Rule-based modelling provides an extendable framework for comparing candidate mechanisms underpinning clathrin polymerisation
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
Linkage relationships and haplotype polymorphism among cichlid Mhc class II B loci
Mapping Haplotype-haplotype Interactions with Adaptive LASSO
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Rule-based geometric modelling
Identification of candidate intergenic risk loci in autism spectrum disorder
A linkage study of candidate loci in familial Parkinson's Disease
Mapping and identification of candidate loci responsible for Peromyscus hybrid overgrowth
Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes
On the use of haplotype phylogeny to detect disease susceptibility loci
Rule-based modelling provides an extendable framework for comparing candidate mechanisms underpinning clathrin polymerisation
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
Linkage relationships and haplotype polymorphism among cichlid Mhc class II B loci
Mapping Haplotype-haplotype Interactions with Adaptive LASSO
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Rule-based geometric modelling
Identification of candidate intergenic risk loci in autism spectrum disorder
A linkage study of candidate loci in familial Parkinson's Disease
Mapping and identification of candidate loci responsible for Peromyscus hybrid overgrowth
Patterns of linkage disequilibrium and haplotype distribution in disease candidate genes
On the use of haplotype phylogeny to detect disease susceptibility loci
Rule-based modelling provides an extendable framework for comparing candidate mechanisms underpinning clathrin polymerisation
A global analysis of Y-chromosomal haplotype diversity for 23 STR loci
Linkage relationships and haplotype polymorphism among cichlid Mhc class II B loci
Mapping Haplotype-haplotype Interactions with Adaptive LASSO
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Rule-based geometric modelling
Identification of candidate intergenic risk loci in autism spectrum disorder
A linkage study of candidate loci in familial Parkinson's Disease