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

2024-05-29

Abstract excerpt

Accurate and complete de novo assembled genomes sustain variant identification and catalyze the discovery of new genomic features and biological functions. However, accurate and precise de novo assemblies of large and complex genomes remains a challenging task. Long-read sequencing data alone or in hybrid mode combined with more accurate short-read sequences facilitate the de novo assembly of genomes. A number of...

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Literature Corpus work
3f7a9764-26ad-5f67-8b09-d2e6ac97fc8f
DOI
10.1101/2024.05.28.595812
Open publication

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Benchmarking of bioinformatics tools for the hybrid de novo assembly of human whole-genome sequencing dataDOI 10.1101/2024.05.28.595812
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