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Alignment-Free Genotyping of Known Variations with MALVA.

Methods in molecular biology (Clifton, N.J.) - 1 Jan 2022

Bernardini Giulia, Denti Luca, Previtali Marco

Abstract excerpt

The discovery and characterization of sequence variations in human populations are crucial in genetic studies. Standard methods for addressing this problem are computationally expensive and highly time consuming, thus impractical for clinical applications, where time is often an issue. When the task is to genotype variations that have been previously annotated, alignment-free methods come to the aid. Here, we...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 35751819
DOI: 10.1007/978-1-0716-2293-3_15

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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