Haplotype Inference in General Pedigrees using the Cluster Variation Method
- Albers, C.A.
- Heskes, T.M.
- Kappen, H.J.
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Contains fulltext : 101018.pdf (publisher's version ) (Closed access
Contains fulltext : 101018.pdf (publisher's version ) (Closed access
In diseases with a complex mode of inheritance, families with multiple affected individuals are diff...
The identification and characterization of genes involved in human disease, especially complex disea...
Recent founder mutations may play important roles in complex diseases and Mendelian disorders. Detec...
Contains fulltext : 34702.pdf (author's version ) (Open Access)We present CVMHAPLO...
Abstract: Inference of haplotypes is indispensable in the studies of human genetics based on haploty...
Motivation: Haplotypes have been attracting increasing attention because of their importance in anal...
This thesis which consists of an introduction and four peer–reviewed origi-nal publications studies ...
Mutation in DNA is the principal cause for differences among human beings, and Single Nucleotide Pol...
Abstract Background Genome sequencing will soon produce haplotype data for individuals. For pedigree...
Background: The linkage phase, or haplotype, is an extra level of information that in addition to ge...
The term “haplotype block” is commonly used in the developing field of haplotype-based inference met...
The genome of all organisms is partitioned into a fixed number of chromosomes. Mammals, including hu...
The haplotype map constructed by the HapMap Project is a valuable resource in the genetic studies of...
Whole-genome association studies present many new statistical and computational challenges due to th...
Integrating dilution-based sequencing and population genotypes for single individual haplotyping Hir...
In diseases with a complex mode of inheritance, families with multiple affected individuals are diff...
The identification and characterization of genes involved in human disease, especially complex disea...
Recent founder mutations may play important roles in complex diseases and Mendelian disorders. Detec...
Contains fulltext : 34702.pdf (author's version ) (Open Access)We present CVMHAPLO...
Abstract: Inference of haplotypes is indispensable in the studies of human genetics based on haploty...
Motivation: Haplotypes have been attracting increasing attention because of their importance in anal...
This thesis which consists of an introduction and four peer–reviewed origi-nal publications studies ...
Mutation in DNA is the principal cause for differences among human beings, and Single Nucleotide Pol...
Abstract Background Genome sequencing will soon produce haplotype data for individuals. For pedigree...
Background: The linkage phase, or haplotype, is an extra level of information that in addition to ge...
The term “haplotype block” is commonly used in the developing field of haplotype-based inference met...
The genome of all organisms is partitioned into a fixed number of chromosomes. Mammals, including hu...
The haplotype map constructed by the HapMap Project is a valuable resource in the genetic studies of...
Whole-genome association studies present many new statistical and computational challenges due to th...
Integrating dilution-based sequencing and population genotypes for single individual haplotyping Hir...
In diseases with a complex mode of inheritance, families with multiple affected individuals are diff...
The identification and characterization of genes involved in human disease, especially complex disea...
Recent founder mutations may play important roles in complex diseases and Mendelian disorders. Detec...