Biology subjects

Piat, L.

Publications and source records attributed to Piat, L..

3 recordsLinked to original sources

bioRxiv2026

A chromosome-scale genome assembly of the Swiss Lolium multiflorum ecotype Tremona reveals a scalable method to purge spurious duplications

Italian ryegrass (Lolium multiflorum) is a key temperate forage species underpinning livestock production in Europe. Genomic resources remain limited by its large (2.2 Gb), repetitive, and highly heterozygous genome. Here, we present a high-quality chromosome-scale genome assembly of the Swiss L. multiflorum ecotype Tremona, collected in 2008 in Ticino, Switzerland, and subsequently incorporated into recurrent breeding cycles in the Swiss breeding program. To address systematic assembly artefacts caused by unresolved haplotypes in our initial PacBio HiFi assembly, we developed ParaLies, a post-assembly tool that identifies and removes artefactual duplications based on sequence divergence while preserving true paralogous gene copies. ParaLies reduced the duplicated BUSCO rate from 16.91% to 6.72% without loss of bona fide genomic content. The resulting assembly has a contig N50 of 15.69 Mb and captures 94% of the expected 2.2-Gb genome size. We further analyzed whole-genome resequencing data from Tremona, additional Swiss ecotypes, and publicly available North American germplasm. Tremona was genetically homogeneous, with no evidence of pronounced recent bottlenecks or substantial within-population structure, and was genetically distinct from the other Swiss ecotypes analyzed. Together, the Tremona genome and ParaLies provide valuable resources for L. multiflorum genomics and breeding and demonstrate a scalable approach for reducing haplotype-induced redundancy in highly heterozygous genomes.

genomics↗

bioRxiv2026

Simulating population pangenomes under coalescent demographic models with MSpangenome

MotivationPangenome variation graphs (PVGs) are increasingly used to represent genomic diversity, yet there is currently no general framework for generating population pangenomes directly from explicit evolutionary histories. Existing simulators typically focus on individual classes of variation and do not integrate these variations within a genealogy-aware framework driven by explicit demographic histories. As a result, evaluating pangenome methods in realistic population-genetic settings remains challenging, and benchmark datasets with known evolutionary ground truth are scarce. ResultsWe present MSpangenome, a genealogy-aware framework that bridges coalescent population genetic simulations and pangenome graph analyses. The pipeline combines ancestry simulation with msprime and a de novo graph construction algorithm to generate PVGs directly from simulated genealogies. By explicitly modeling recombination, demographic history and incomplete lineage sorting, MSpangenome produces structurally complex pangenomes in which nested and overlapping structural variants emerge naturally from the underlying genealogies, while their evolutionary history and graph topology remain known by construction. This provides a general framework for generating realistic population pangenomes and establishing ground-truth datasets for methodological evaluation. We demonstrate its utility by generating population-scale pangenomes and using them as controlled references to benchmark the widely used graph construction tools, PGGB and Minigraph-Cactus. Our analyses reveal contrasting performance regimes across levels of sequence diversity, sample sizes and classes of structural variation, highlighting the value of simulation-based benchmarking for identifying reconstruction errors that are hard to detect using empirical datasets alone. Availability and implementationMSpangenome is implemented in Python, fully containerized, freely available at https://forge.inrae.fr/pangepop/MSpangepop and mirrored at https://github.com/inrae/MSpangepop.

bioinformatics↗

bioRxiv2026

A reference genome assembly for Quercus canariensis Willd

The authors have withdrawn this manuscript because the sequenced individual was misidentified as Quercus canariensis following a label swap and was subsequently confirmed to be Quercus pyrenaica. A corrected manuscript focusing on Q. pyrenaica will be submitted shortly to avoid propagating the incorrect species attribution. Therefore, the authors do not wish this work to be cited as reference for the project. If you have any questions, please contact the corresponding author.

genetics↗