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Lucas R. van Dijk

dblp:424/3684 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2025
0000-0002-7565-5859ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
multiple sequence alignment
0.912025
Fast and exact gap-affine partial order alignment with POASTA · Bioinform. 2025
Bioinformatics and computational biology › sequence alignment › graph-based alignment
partial order alignment
0.912025
Fast and exact gap-affine partial order alignment with POASTA · Bioinform. 2025
Bioinformatics and computational biology
sequence analysis
0.912025
Fast and exact gap-affine partial order alignment with POASTA · Bioinform. 2025

Methods — techniques the papers use, named apart from their topics

gap-affine alignment · 0.9
YearPublicationVenuePosition
2025 Fast and exact gap-affine partial order alignment with POASTA
abstract
MOTIVATION: Partial order alignment is a widely used method for computing multiple sequence alignments, with applications in genome assembly and pangenomics, among many others. Current algorithms to compute the optimal, gap-affine partial order alignment do not scale well to larger graphs and sequences. While heuristic approaches exist, they do not guarantee optimal alignment and sacrifice alignment accuracy. RESULTS: We present POASTA, a new optimal algorithm for partial order alignment that exploits long stretches of matching sequence between the graph and a query. We benchmarked POASTA against the state-of-the-art on several diverse bacterial gene datasets and demonstrated an average speed-up of 4.1× and up to 9.8×, using less memory. POASTA's memory scaling characteristics enabled the construction of much larger POA graphs than previously possible, as demonstrated by megabase-length alignments of 342 Mycobacterium tuberculosis sequences. AVAILABILITY AND IMPLEMENTATION: POASTA is available on Github at https://github.com/broadinstitute/poasta.
Lucas R. van Dijk, Abigail L. Manson, Ashlee M. Earl, Kiran V. Garimella, Thomas Abeel
Bioinform.1