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de Ferran, V.

Publications and source records attributed to de Ferran, V..

3 recordsLinked to original sources

High-Quality De Novo Genome Assembly for the Galapagos Endemic Lava Gull Using Oxford Nanopore Technologies

High-quality reference genomes permit deeper investigation into species evolution and provide insight into species management and conservation. Next-generation sequencing technologies, such as Oxford Nanopore Technologies, allow researchers to generate high-accuracy long-read genetic data in real-time from anywhere in the world, increasing accessibility to sequence data. The lava gull (Leucophaeus fuliginosus), an endemic bird species of the Galapagos archipelago, is the worlds rarest gull with an estimated population of 300 to 600 individuals. Little genetic research has been done on this species due to its solitary nature and small population size. Here we present a chromosome-level reference genome assembly of an adult female lava gull, generated using ultra-long reads from the Oxford Nanopore Ultra-Long DNA Sequencing Kit and a PromethION 2 Solo device. Initial sequencing generated 1.78 million reads, consisting of 29.6 gigabases (Gbp), with a mean Q-score of 17.8 at an average 22.5x coverage. Our final assembly has a total length of 1.31 Gbp, with 450 scaffolds, and a scaffold N50 of 85.1 Mbp and contig N50 of 42.8 Mbp. The generation of a high-quality whole genome for the lava gull is an important step for investigation into the species phylogeography and population genetics.

genomics↗

First Whole-Genome Assembly of the Galapagos Petrel (Pterodroma phaeopygia) Using Oxford Nanopore Sequencing to Advance Conservation Genomics in a Critically Endangered Seabird

The Galapagos petrel (Pterodroma phaeopygia) is a critically endangered procellariiform seabird endemic to the Galapagos Islands. Once abundant, its populations have sharply declined due to invasive predators, habitat degradation, and destruction of nest burrows. Although the species is distributed across several islands, the demographics of each population and their genetic relationships are poorly understood. To facilitate future studies of population structure and connectivity, we present the first high-quality reference genome for the Galapagos petrel. The genome was assembled from ultra-long Oxford Nanopore sequence data collected from an adult female sampled on San Cristobal Island. Sequencing was performed at the Galapagos Science Center, enabling local capacity-building and compliance with strict sample import-export regulations of endangered species. The final nuclear genome assembly spans 1.35 Gb in length, with average coverage of 36.07x, scaffold N50 of 74.2 Mb, and a BUSCO aves lineage completeness of 99.95%. The genome comprises 41 pseudo-chromosomes, with 23 spanning from telomere to telomere and 16, including W and Z chromosomes, containing a single telomere. Chromosomal-level scaffolding by reference was performed using the genome of Corys shearwater (Calonectris borealis) GCA_964196065.2 (Aranega et al., 2024), a related species. The Galapagos petrel reference genome represents a foundational tool for comparative genomics, conservation biology, and functional studies of island-endemic avifauna. It will also facilitate future efforts to characterize genetic diversity, structural variation, and adaptive responses in this critically endangered species.

genomics↗

Large-scale identification of microsatellite loci from multiple otter (Mammalia, Carnivora, Lutrinae) species using whole genome sequence data

The development of molecular studies on elusive, rare, and/or poorly known species faces challenges due to the lack of suitable markers. Species-specific microsatellite markers minimize bias, offer better performance, and are cost-effective, aiding the development of population genetic studies. The use of whole-genome sequences allows for the development of species-specific microsatellite markers and their survey in closely related species, enabling the discovery of shared markers that can facilitate comparative studies. Lutrinae includes 14 extant species of otters. Despite their worrisome conservation status, due to inherent characteristics of these species that make their study difficult by traditional methods, many of them lack reliable population genetic data, limiting conservation efforts. In this study, we employed a multi-taxon approach to identify a large number of novel microsatellite loci for 11 of the 14 otter species, assessing whether the identified loci were shared among different taxa. We identified a total of 23,320 microsatellite loci across 11 species, which were reduced to 12,573 after stringent filtering criteria. Primer design was completed successfully for 420 and 259 unique loci, considering two minimum melting temperatures. We validated marker efficiency by testing the 81 loci designed for two Asian species. Of these, 51 loci yielded reliable microsatellite genotypes in both species, with 34 showing allelic variation in at least one of them. These results demonstrate that these markers are applicable in empirical genotyping for both their target and closely related ones.

genomics↗