BMC BioinformaticsBioinformaticsPeer-reviewed journal article
Hap10: reconstructing accurate and long polyploid haplotypes using linked reads
Sina MajidianiD, Mohammad Hossein KahaeiiD, Dick de RidderiD
Abstract
BackgroundHaplotype information is essential for many genetic and genomic analyses, including genotype-phenotype associations in human, animals and plants. Haplotype assembly is a method for reconstructing haplotypes from DNA sequencing reads. By the advent of new sequencing technologies, new algorithms are needed to ensure long and accurate haplotypes. While a few linked-read haplotype assembly algorithms are available for diploid genomes, there are no algorithms yet for polyploids. ResultsThe first haplotyping algorithm designed for 10X linked reads generated from a polyploid genome is presented, built on a typical short-read haplotyping method, SDhaP. Using the input aligned reads and called variants, the haplotype-relevant information is extracted. Next, reads with the same barcodes are combined to produce molecule-specific fragments. Then, these fragments are clustered into strongly connected components which are then used as input of a haplotype assembly core in order to estimate accurate and long haplotypes. ConclusionsHap10 is a novel algorithm for haplotype assembly of polyploid genomes using linked reads. The performance of the algorithms is evaluated in a number of simulation scenarios and its applicability is demonstrated on a real dataset of sweet potato.
- organism: plant (other)
- assay: whole-genome sequencing
- research focus: variant calling
- approach: statistical model
- Citations
- 18
- FWCI
- 1.05
- Field percentile
- top 26%
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