ArticleBMC genomics2013
A highly accurate heuristic algorithm for the haplotype assembly problem.
Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 36 citations in OpenAlex.
- Minimum error correction-based haplotype assembly: Considerations for long read data.PloS one · 2020Article
- NGS based haplotype assembly using matrix completion.PloS one · 2019Article
- Efficient algorithms for polyploid haplotype phasing.BMC genomics · 2018Article
- Article
- Dense and accurate whole-chromosome haplotyping of individual genomes.Nature communications · 2017Article
- Rising Strengths Hong Kong SAR in Bioinformatics.Interdisciplinary sciences, computational life sciences · 2017Review
- PWHATSHAP: efficient haplotyping for future generation sequencing.BMC bioinformatics · 2016Article
- Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm.BMC bioinformatics · 2015Article
- Whole-genome haplotyping approaches and genomic medicine.Genome medicine · 2014Article
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Authors and funding
3 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundSingle 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.
resultsWe 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.
conclusionsWe 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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