#35 · Genomics
Chromosome-scale diploid and cetacean genomes extend assembly to new taxa
The dominant thread is chromosome-scale genome construction in eukaryotes. The franciscana dolphin assembly reports 3.13 Gb across 22 chromosomes, with scaffold N50 of 111.18 Mb and BUSCO completeness of 99.42%, extending chromosome-level references to an endangered cetacean. The prairie and meadow vole study uses a single-library PacBio HiFi and CiFi approach to produce chromosome-scale diploid assemblies that reveal Y divergence and a prairie-vole Avpr1a duplication. The king scallop study and the olfactory receptor framework instead apply genomic data to population questions: 15 chromosomal inversions underlie localised differentiation among 168 sequenced individuals, and a duplication-to-loss ratio flags historical bottlenecks across felids and ursids. What is new is the taxonomic breadth of chromosome-scale diploid and cetacean references and the use of gene-family evolution metrics to read demographic history from genomic data.
Published papers
Single-library chromosome-scale diploid assemblies of vole genomes resolve a species-specific duplication implicated in pair bonding.
Single-library PacBio HiFi and CiFi approach yields chromosome-scale diploid prairie and meadow vole genomes, revealing Y divergence and a prairie-vole Avpr1a…
Preprints
A chromosome-level genome of the franciscana dolphin, Pontoporia blainvillei
Presents a chromosome-level genome assembly (3.13 Gb, 22 chromosomes, scaffold N50 111.18 Mb, BUSCO 99.42%) for the endangered franciscana dolphin, built from…
A comparative genomics framework for identifying historical population bottlenecks using olfactory receptor gene evolution
Introduces a duplication-to-loss ratio (DLR) metric from olfactory receptor gene evolution to flag historical population bottlenecks across felids, ursids and…
Multiple chromosomal inversions shape the genetic structure of a commercial bivalve
Whole-genome sequencing of 168 king scallops identifies 15 chromosomal inversions that drive localised genetic differentiation despite high gene flow.
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