Benchmarking of bioinformatics tools for the hybrid de novo assembly of human and non-human whole-genome sequencing data

Accurate and complete de novo genome assemblies enable variant identification and the discovery of novel genomic features and biological functions. However, de novo assemblies of large and complex genomes remain challenging. Long-read sequencing data, alone or combined with short-read data, facilita...

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Hlavní autoři:	Adrián Muñoz-Barrera, Luis A. Rubio-Rodríguez, David Jáspez, Almudena Corrales, Itahisa Marcelino-Rodriguez, Lourdes Ortiz, Pablo Mendoza, José M. Lorenzo-Salazar, Rafaela González-Montelongo, Carlos Flores
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 2025-01-01
Edice:	Computational and Structural Biotechnology Journal
Témata:	Long-read sequencing Nanopore WGS De novo genome assembly
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S2001037025002867
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