ArticleJournal of bioinformatics and computational biology2009
An almost linear time algorithm for a general haplotype solution on tree pedigrees with no recombination and its extensions.
Article in Journal of bioinformatics and computational biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- A Genetic Map of Ostrich Z Chromosome and the Role of Inversions in Avian Sex Chromosome Evolution.Genome biology and evolution · 2018Article
- GenomeLaser: fast and accurate haplotyping from pedigree genotypes.Bioinformatics (Oxford, England) · 2015Article
- Article
- Detection of recombination events, haplotype reconstruction and imputation of sires using half-sib SNP genotypes.Genetics, selection, evolution : GSE · 2014Article
- A genetic linkage map of sole (Solea solea): a tool for evolutionary and comparative analyses of exploited (flat)fishes.PloS one · 2014Article
- Haplotype reconstruction in large pedigrees with untyped individuals through IBD inference.Journal of computational biology : a journal of computational molecular cell biology · 2011Article
- Comparison of analyses of the QTLMAS XIV common dataset. II: QTL analysis.BMC proceedings · 2011Article
- Accurate HLA type inference using a weighted similarity graph.BMC bioinformatics · 2010Article
- Efficient identification of identical-by-descent status in pedigrees with many untyped individuals.Bioinformatics (Oxford, England) · 2010Article
- A novel approach for haplotype-based association analysis using family data.BMC bioinformatics · 2010Article
- Detecting genome-wide haplotype polymorphism by combined use of Mendelian constraints and local population structure.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2010Article
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2 authors.
Funding
Abstract
We study the haplotype inference problem from pedigree data under the zero recombination assumption, which is well supported by real data for tightly linked markers (i.e. single nucleotide polymorphisms (SNPs)) over a relatively large chromosome segment. We solve the problem in a rigorous mathematical manner by formulating genotype constraints as a linear system of inheritance variables. We then utilize disjoint-set structures to encode connectivity information among individuals, to detect constraints from genotypes, and to check consistency of constraints. On a tree pedigree without missing data, our algorithm can output a general solution as well as the number of total specific solutions in a nearly linear time O(mn . alpha(n)), where m is the number of loci, n is the number of individuals and alpha is the inverse Ackermann function, which is a further improvement over existing ones. We also extend the idea to looped pedigrees and pedigrees with missing data by considering existing (partial) constraints on inheritance variables. The algorithm has been implemented in C++ and will be incorporated into our PedPhase package. Experimental results show that it can correctly identify all 0-recombinant solutions with great efficiency. Comparisons with other two popular algorithms show that the proposed algorithm achieves 10 to 10(5)-fold improvements over a variety of parameter settings. The experimental study also provides empirical evidences on the complexity bounds suggested by theoretical analysis.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.