顺序装配
算法
计算机科学
德布鲁因图
杂交基因组组装
散列函数
图形
DNA测序
基因组
源代码
移相器
康蒂格
计算生物学
理论计算机科学
生物
遗传学
DNA
基因
工程类
转录组
操作系统
计算机安全
电气工程
基因表达
作者
Laura González,David Guevara-Barrientos,Daniela Lozano‐Arce,Juanita Gil,Jorge Díaz-Riaño,Erick Duarte,Germán I. Andrade,Juan Camilo Bojacá,Maria Camila Hoyos,Christian Chavarro,Natalia Guayazán Palacios,Luis Alberto Chica Cárdenas,Maria Camila Buitrago Acosta,Edwin Bautista,Miller Trujillo,Jorge Duitama
标识
DOI:10.1101/2022.08.30.505891
摘要
Abstract Producing de-novo genome assemblies for complex genomes is possible thanks to long-read DNA sequencing technologies. However, maximizing the quality of assemblies based on long reads is a challenging task that requires the development of specialized data analysis techniques. In this paper, we present new algorithms for assembling long-DNA sequencing reads from haploid and diploid organisms. The assembly algorithm builds an undirected graph with two vertices for each read based on minimizers selected by a hash function derived from the k-mers distribution. Statistics collected during the graph construction are used as features to build layout paths by selecting edges, ranked by a likelihood function that is calculated from the inferred distributions of features on a subset of safe edges. For diploid samples, we integrated a reimplementation of the ReFHap algorithm to perform molecular phasing. The phasing procedure is used to remove edges connecting reads assigned to different haplotypes and to obtain a phased assembly by running the layout algorithm on the filtered graph. We ran the implemented algorithms on PacBio HiFi and Nanopore sequencing data taken from bacteria, yeast, Drosophila , rice, maize, and human samples. Our algorithms showed competitive efficiency and contiguity of assemblies, as well as superior accuracy in some cases, as compared to other currently used software. We expect that this new development will be useful for researchers building genome assemblies for different species.
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