Fast and accurate mapping of long reads to complete genome assemblies with VerityMap

  1. Pavel A. Pevzner3
  1. 1Graduate Program in Bioinformatics and Systems Biology, University of California, San Diego, California 92093, USA;
  2. 2Center for Algorithmic Biotechnology, Saint Petersburg State University, Saint Petersburg, 199034, Russia;
  3. 3Department of Computer Science and Engineering, University of California, San Diego, California 92093, USA
  1. 4 These authors contributed equally to this work.

  • Corresponding author: abzikadze{at}ucsd.edu
  • Abstract

    Recent advancements in long-read sequencing have enabled the telomere-to-telomere (complete) assembly of a human genome and are now contributing to the haplotype-resolved complete assemblies of multiple human genomes. Because the accuracy of read mapping tools deteriorates in highly repetitive regions, there is a need to develop accurate, error-exposing (detecting potential assembly errors), and diploid-aware (distinguishing different haplotypes) tools for read mapping in complete assemblies. We describe the first accurate, error-exposing, and partially diploid-aware VerityMap tool for long-read mapping to complete assemblies.

    Footnotes

    • Received April 26, 2022.
    • Accepted November 9, 2022.

    This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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