A highly accurate heuristic algorithm for the haplotype assembly problem.

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

27 Scopus Citations
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Original languageEnglish
Article numberS2
Journal / PublicationBMC Genomics
Volume14 Suppl 2
Online published28 May 2013
Publication statusPublished - 2013

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Abstract

Single nucleotide polymorphisms (SNPs) are the most common form of genetic variation in human DNA. The sequence of SNPs in each of the two copies of a given chromosome in a diploid organism is referred to as a haplotype. Haplotype information has many applications such as gene disease diagnoses, drug design, etc. The haplotype assembly problem is defined as follows: Given a set of fragments sequenced from the two copies of a chromosome of a single individual, and their locations in the chromosome, which can be pre-determined by aligning the fragments to a reference DNA sequence, the goal here is to reconstruct two haplotypes (h1, h2) from the input fragments. Existing algorithms do not work well when the error rate of fragments is high. Here we design an algorithm that can give accurate solutions, even if the error rate of fragments is high. We first give a dynamic programming algorithm that can give exact solutions to the haplotype assembly problem. The time complexity of the algorithm is O(n × 2t × t), where n is the number of SNPs, and t is the maximum coverage of a SNP site. The algorithm is slow when t is large. To solve the problem when t is large, we further propose a heuristic algorithm on the basis of the dynamic programming algorithm. Experiments show that our heuristic algorithm can give very accurate solutions. We have tested our algorithm on a set of benchmark datasets. Experiments show that our algorithm can give very accurate solutions. It outperforms most of the existing programs when the error rate of the input fragments is high.

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A highly accurate heuristic algorithm for the haplotype assembly problem. / Deng, Fei; Cui, Wenjuan; Wang, Lusheng.
In: BMC Genomics, Vol. 14 Suppl 2, S2, 2013.

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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