FNphasing: A Novel Fast Heuristic Algorithm for Haplotype Phasing Based on Flow Network Model

No abstract is available for this paper.

• Publication year

  2013

• Venue

  IEEE/ACM Transactions on Computational Biology & Bioinformatics

• Publication date

  2013-03-01

• Fields of study

  Biology, Medicine, Computer Science

• Identifiers
  DOI 10.1109/TCBB.2013.18PMID 23929861
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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• Haplotype inference.

  2012cited by this paper
• Phasing of many thousands of genotyped samples.

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• Supplementary Information for ‘ Improved whole chromosome phasing for disease and population genetic studies ’

  2012cited by this paper
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  2011cited by this paper
• SplittingHeirs: inferring haplotypes by optimizing resultant dense graphs

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  2010cited by this paper
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  2009cited by this paper
• Next-generation sequencing transforms today's biology

  2008cited by this paper
• A better block partition and ligation strategy for individual haplotyping

  2008cited by this paper
• Next-generation DNA sequencing

  2008influential reference
• A new multipoint method for genome-wide association studies by imputation of genotypes

  2007cited by this paper
• A second generation human haplotype map of over 3.1 million SNPs

  2007cited by this paper
• Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering.

  2007cited by this paper
• A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase.

  2006cited by this paper
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  2006cited by this paper
• Islands of tractability for parsimony haplotyping

  2006cited by this paper
• Islands of Tractability for Parsimony Haplotyping

  2005cited by this paper
• A Practical Algorithm for Haplotyping by Maximum Parsimony

  2005cited by this paper
• Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation.

  2005cited by this paper
• Haploview: analysis and visualization of LD and haplotype maps

  2005cited by this paper
• A Note on Efficient Computation of Haplotypes via Perfect Phylogeny

  2004cited by this paper
• Haplotyping Populations by Pure Parsimony: Complexity of Exact and Approximation Algorithms

  2004cited by this paper
• Haplotype inference by maximum parsimony

  2003cited by this paper
• The Haplotyping problem: An overview of computational models and solutions

  2003cited by this paper
• A comparison of bayesian methods for haplotype reconstruction from population genotype data.

  2003cited by this paper
• Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms.

  2002cited by this paper
• A Survey of Computational Methods for Determining Haplotypes

  2002cited by this paper
• Haplotype inference in random population samples.

  2002cited by this paper
• Generating samples under a Wright-Fisher neutral model of genetic variation

  2002cited by this paper
• Haplotyping as perfect phylogeny: conceptual framework and efficient solutions

  2002cited by this paper
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  2001cited by this paper
• Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21

  2001cited by this paper
• High-resolution haplotype structure in the human genome

  2001cited by this paper
• A physical map of the human genome

  2001cited by this paper
• The sequence of the human genome (abstract only)

  2001cited by this paper
• A new statistical method for haplotype reconstruction from population data.

  2001cited by this paper
• Sequence variability and candidate gene analysis in complex disease: association of mu opioid receptor gene variation with substance dependence.

  2000cited by this paper
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  1999cited by this paper
• Characterization of single-nucleotide polymorphisms in coding regions of human genes

  1999cited by this paper
• Sequence variation in the human angiotensin converting enzyme

  1999cited by this paper
• Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.

  1998cited by this paper
• Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population.

  1995cited by this paper
• Low nucleotide diversity in man.

  1991cited by this paper
• Inference of haplotypes from PCR-amplified samples of diploid populations.

  1990cited by this paper
• On measures of gametic disequilibrium.

  1988cited by this paper
• Sequence the Human Genome

  1986influential reference
• Accounting for Decay of Linkage Disequilibrium in Haplotype Inference and Missing-data Imputation

  year unknowncited by this paper

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