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Advancements in long-read genome sequencing technologies and algorithms
被引:15
|作者:
Espinosa, Elena
[1
]
Bautista, Rocio
[2
]
Larrosa, Rafael
[1
,2
]
Plata, Oscar
[1
]
机构:
[1] Univ Malaga, Dept Comp Architecture, Louis Pasteur 35,Campus Teatinos, Malaga 29071, Spain
[2] Univ Malaga, Supercomp & Bioinnovat Ctr, C Severo Ochoa 34, Malaga 29590, Spain
来源:
关键词:
Genome assembly;
Hybrid assembly;
Long reads;
CHROMOSOME-LEVEL GENOME;
PACBIO;
ASSEMBLIES;
ANNOTATION;
GENERATION;
ACCURATE;
TIME;
TOOL;
GROUPER;
HIFI;
D O I:
10.1016/j.ygeno.2024.110842
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
The recent advent of long read sequencing technologies, such as Pacific Biosciences (PacBio) and Oxford Nanopore technology (ONT), have led to substantial improvements in accuracy and computational cost in sequencing genomes. However, de novo whole-genome assembly still presents significant challenges related to the quality of the results. Pursuing de novo whole-genome assembly remains a formidable challenge, underscored by intricate considerations surrounding computational demands and result quality. As sequencing accuracy and throughput steadily advance, a continuous stream of innovative assembly tools floods the field. Navigating this dynamic landscape necessitates a reasonable choice of sequencing platform, depth, and assembly tools to orchestrate high-quality genome reconstructions. This comprehensive review delves into the intricate interplay between cutting-edge long read sequencing technologies, assembly methodologies, and the ever-evolving field of genomics. With a focus on addressing the pivotal challenges and harnessing the opportunities presented by these advancements, we provide an in-depth exploration of the crucial factors influencing the selection of optimal strategies for achieving robust and insightful genome assemblies.
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页数:12
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