Haplotyping estimation from aligned single nucleotide polymorphism fragments has attracted increasing attention in recent years because of its importance in the analysis of fine-scale genetic data. Its application fields range from mapping of complex disease genes to inferring population histories, passing through designing drugs, functional genomics, and pharmacogenetics. The literature proposes several criteria for haplotyping populations, each of them characterized by biological motivations. One of the most important haplotyping criteria is parsimony, which consists of finding the minimum number of haplotypes necessary to explain a given set of genotypes. Parsimonious haplotype estimation is an NP-hard problem for which the literature ha...
Mutation in DNA is the principal cause for differences among human beings, and Single Nucleotide Pol...
Amixed integer linear programming model to reconstruct phylogenies from single nucleotide polymorphi...
Background: Phylogeny estimation from aligned haplotype sequences has attracted more and more attent...
The Pure Parsimony Haplotyping (PPH) problem is a NP-hard combinatorial optimization problem that co...
The Pure Parsimony Haplotyping (PPH) problem is a NP-hard combinatorial optimization problem that co...
The Pure Parsimony Haplotyping (PPH) problem is a NP-hard combinatorial optimization problem that co...
AbstractSimilarity and diversity among individuals of the same species are expressed in small DNA va...
Similarity and diversity among individuals of the same species are expressed in small DNA variations...
Single Nucleotide Polymorphisms (SNPs) are the most common form of variations in the human genome. C...
Motivation: Haplotypes have been attracting increasing attention because of their importance in anal...
We present two integer programming models for the Haplotype Inference by Pure Parsimony problem. The...
In this paper we address the pure parsimony haplotyping problem: Find a minimum number of haplotypes...
The genome of all organisms is partitioned into a fixed number of chromosomes. Mammals, including hu...
The knowledge of nucleotides chains that compose the double DNA chain of an individual has a relevan...
Abstract. Parsimony haplotyping is the problem of finding a smallest size set of haplotypes that can...
Mutation in DNA is the principal cause for differences among human beings, and Single Nucleotide Pol...
Amixed integer linear programming model to reconstruct phylogenies from single nucleotide polymorphi...
Background: Phylogeny estimation from aligned haplotype sequences has attracted more and more attent...
The Pure Parsimony Haplotyping (PPH) problem is a NP-hard combinatorial optimization problem that co...
The Pure Parsimony Haplotyping (PPH) problem is a NP-hard combinatorial optimization problem that co...
The Pure Parsimony Haplotyping (PPH) problem is a NP-hard combinatorial optimization problem that co...
AbstractSimilarity and diversity among individuals of the same species are expressed in small DNA va...
Similarity and diversity among individuals of the same species are expressed in small DNA variations...
Single Nucleotide Polymorphisms (SNPs) are the most common form of variations in the human genome. C...
Motivation: Haplotypes have been attracting increasing attention because of their importance in anal...
We present two integer programming models for the Haplotype Inference by Pure Parsimony problem. The...
In this paper we address the pure parsimony haplotyping problem: Find a minimum number of haplotypes...
The genome of all organisms is partitioned into a fixed number of chromosomes. Mammals, including hu...
The knowledge of nucleotides chains that compose the double DNA chain of an individual has a relevan...
Abstract. Parsimony haplotyping is the problem of finding a smallest size set of haplotypes that can...
Mutation in DNA is the principal cause for differences among human beings, and Single Nucleotide Pol...
Amixed integer linear programming model to reconstruct phylogenies from single nucleotide polymorphi...
Background: Phylogeny estimation from aligned haplotype sequences has attracted more and more attent...