Abstract Background Haplotype assembly, reconstructing haplotypes from sequence data, is one of the major computational problems in bioinformatics. Most of the current methodologies for haplotype assembly are designed for diploid individuals. In recent years, genomes having more than two sets of homologous chromosomes have attracted many research groups that are interested in the genomics of disease, phylogenetics, botany and evolution. However, there is still a lack of methods for reconstructing polyploid haplotypes. Results In this work, the minimum error correction with genotype information (MEC/GI) model, an important combinatorial model for haplotyping a single individual, is used to study the triploid individual haplotype reconstructi...
Abstract. Single nucleotide polymorphisms (SNPs) are the most fre-quent form of human genetic variat...
The next phase of human genomics will involve large-scale screens of populations for significant DNA...
The Minimum Error Correction (MEC) is an important model for haplotype reconstruction from SNP fragm...
Single nucleotide polymorphisms (SNPs) are the most frequent form of human genetic variation. They a...
Critical to the understanding of the genetic basis for com-plex diseases is the modeling of human va...
The determination of feature maps, such as STSs (sequence tag sites), SNPs (single nucleotide polymo...
Abstract Background Due to the difficulty in separating two (paternal and maternal) copies of a chro...
The genome of all organisms is partitioned into a fixed number of chromosomes. Mammals, including hu...
Many phenotypes such as genetic disorders may be hereditary while others may be influenced by the en...
The investigation of genetic differences among humans has given evidence that mutations in DNA seque...
Critical to the understanding of the genetic basis for complex diseases is the modeling of human var...
In diploid genomes, haplotype assembly is the computational problem of reconstructing the two parent...
The next phase of human genomics will involve large-scale screens of populations for signif-icant DN...
Abstract. Single nucleotide polymorphism (SNP) is the most frequent form of DNA variation. The set o...
In diploid genomes, haplotype assembly is the computational problem of reconstructing the two parent...
Abstract. Single nucleotide polymorphisms (SNPs) are the most fre-quent form of human genetic variat...
The next phase of human genomics will involve large-scale screens of populations for significant DNA...
The Minimum Error Correction (MEC) is an important model for haplotype reconstruction from SNP fragm...
Single nucleotide polymorphisms (SNPs) are the most frequent form of human genetic variation. They a...
Critical to the understanding of the genetic basis for com-plex diseases is the modeling of human va...
The determination of feature maps, such as STSs (sequence tag sites), SNPs (single nucleotide polymo...
Abstract Background Due to the difficulty in separating two (paternal and maternal) copies of a chro...
The genome of all organisms is partitioned into a fixed number of chromosomes. Mammals, including hu...
Many phenotypes such as genetic disorders may be hereditary while others may be influenced by the en...
The investigation of genetic differences among humans has given evidence that mutations in DNA seque...
Critical to the understanding of the genetic basis for complex diseases is the modeling of human var...
In diploid genomes, haplotype assembly is the computational problem of reconstructing the two parent...
The next phase of human genomics will involve large-scale screens of populations for signif-icant DN...
Abstract. Single nucleotide polymorphism (SNP) is the most frequent form of DNA variation. The set o...
In diploid genomes, haplotype assembly is the computational problem of reconstructing the two parent...
Abstract. Single nucleotide polymorphisms (SNPs) are the most fre-quent form of human genetic variat...
The next phase of human genomics will involve large-scale screens of populations for significant DNA...
The Minimum Error Correction (MEC) is an important model for haplotype reconstruction from SNP fragm...