A Survey of Computational Methods for Determining Haplotypes

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It is widely anticipated that the study of variation in the human genome will provide a means of predicting risk of a variety of complex diseases. Single nucleotide polymorphisms (SNPs) are the most common form of genomic variation. Haplotypes have been suggested as one means for reducing the complexity of studying SNPs. In this paper we review some of the computational approaches that have been taking for determining haplotypes and suggest new approaches.

Bjarni V. Halldórsson, Vineet Bafna, Nathan

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Complex Diseases | Computational Biology | Human Genome | RECOMB 2002 | Single Nucleotide Polymorphisms |

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Added	03 Dec 2009
Updated	03 Dec 2009
Type	Conference
Year	2002
Where	RECOMB
Authors	Bjarni V. Halldórsson, Vineet Bafna, Nathan Edwards, Ross Lippert, Shibu Yooseph, Sorin Istrail

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A Survey of Computational Methods for Determining Haplotypes

Complex Diseases | Computational Biology | Human Genome | RECOMB 2002 | Single Nucleotide Polymorphisms |

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