Phylogenetic variation, recombination rate evolution, and comparative genome structure and organization have typically been explored in isolation. The chromosomal and genomic context of selected genetic markers in phylogenetic studies is usually unknown, given the fragmented nature of most genome assemblies. It is now established that the position of markers in the genome can strongly influence the inferred phylogeny, often not reflecting speciation patterns and subsequent bifurcating tree structure but rather post-speciation introgression. The recent availability of chromosome-level genome assemblies and advances in estimating genome-wide recombination rates have created opportunities to jointly understand the interplay of chromosome evolution, the landscape of recombination, and phylogenetic signal.

Barcelona to host the Leading Event in Evolutionary Biology ESEB 2025

Background Anemonefish association with sea anemones is a prime example of mutualistic symbiosis. These fish live inside the sea anemone, benefitting from the protection of its toxic nematocysts, and…

Séquencer le génome de 4 500 espèces marines, c’est l’objectif du programme de recherche ATLASea dont la première expédition a eu lieu à Dinard, en Bretagne. Pendant huit ans, les scientifiques vont c...

Researchers used artificial intelligence in large genomics studies to fill in gaps in patient information and improve predictions, but new research uncovers false positives and misleading correlations...

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Supernumerary B chromosomes contribute to intraspecific karyotypic variation. B chromosomes have bee

Dioecy, defined by the presence of either female or male flowers on separate individual plants, is r