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Arvestad, L.

Publications and source records attributed to Arvestad, L..

2 recordsLinked to original sources

Scalable distance-based phylogeny inference using divide-and-conquer

Distance-based methods for inferring evolutionary trees are important subroutines in computational biology, sometimes as a first step in a statistically more robust phylogenetic method. The most popular method is Neighbor Joining, mainly to to its relatively good accuracy, but Neighbor Joining has a cubic time complexity, which limits its applicability on larger datasets. Similar but faster algorithms have been suggested, but the overall time complexity remains essentially cubic as long as the input is a distance matrix. This paper investigates a randomized divide-and-conquer heuristic, dnctree, which selectively estimates pairwise sequence distances and infers a tree by connecting increasingly large subtrees. The divide-and-conquer approach avoids computing all pairwise distances and thereby saves both time and memory. The time complexity is at worst quadratic, and seems to scale like O(n lg n) on average. A simple Python implementation, dnctree, available on GitHub and PyPI.org, has been tested and we show that it is a scalable solution. In fact, it is applicable to very large datasets even as plain Python program.

bioinformatics↗

The mitogenome of Norway spruce and a reappraisal of mitochondrial recombination in plants

Plant mitogenomes can be difficult to assemble because they are structurally dynamic and prone to intergenomic DNA transfers, leading to the unusual situation where an organelle genome is far outnumbered by its nuclear counterparts. As a result, comparative mitogenome studies are in their infancy and some key aspects of genome evolution are still known mainly from pre-genome, qualitative methods. To help address these limitations, we combined machine learning and in silico enrichment of mitochondrial-like long reads to assemble the bacterial-sized mitogenome of Norway spruce (Pinaceae: Picea abies). We conducted comparative analyses of repeat abundance, intergenomic transfers, substitution and rearrangement rates, and estimated repeat-by-repeat homologous recombination rates. Prompted by our discovery of highly recombinogenic small repeats in P. abies, we assessed the genomic support for the prevailing hypothesis that intramolecular recombination is predominantly driven by repeat length, with larger repeats facilitating DNA exchange more readily. Overall, we found mixed support for this view: recombination dynamics were heterogeneous across vascular plants and highly active small repeats (ca. 200 bp) were present in about a third of studied mitogenomes. As in previous studies, we did not observe any robust relationships among commonly-studied genome attributes, but we identify variation in recombination rates as a underinvestigated source of plant mitogenome diversity.

genomics↗