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Tricomi, F. F.

Publications and source records attributed to Tricomi, F. F..

2 recordsLinked to original sources

MirMachine 2: a scalable, evolutionarily informed pipeline for microRNA annotation and comparative genomics across thousands of animal genomes

Genome sequencing is rapidly outpacing the annotation of conserved regulatory elements, limiting the evolutionary and comparative insights that can be extracted from expanding genome collections. MicroRNAs are among the most conserved and phylogenetically informative genes, yet automated annotation has remained difficult to scale while preserving evolutionary interpretability. Here we present MirMachine 2, an evolutionarily informed framework that combines curated reference models, lineage-aware scoring, and adaptive filtering to enable robust genome-wide microRNA annotation at scale. Applying this to thousands of animal genomes reveals that many apparent absences of conserved microRNAs reflect methodological bias rather than biological loss, particularly in underrepresented lineages. By enabling consistent and interpretable comparison of microRNA complements across large datasets, MirMachine 2 establishes scalable microRNA annotation as a practical foundation for genome-scale evolutionary and comparative genomics.

bioinformatics↗

The mouse pangenome reveals the structural complexity of the murine protein coding landscape

We present the first mouse pangenome consisting of 17 high-quality inbred mouse strain genomes with complete annotation. This collection includes 12 widely used classical laboratory strains and 5 wild-derived strains. We have fully resolved previously incomplete genomic regions, including the major histocompatibility complex (MHC), the defensin cluster, T-cell receptor, and Ly49 complexes. Hundreds of non-reference genes identified in previous publications not found in GRCm39, like Defa1, Raet1a, and Klra20 (Ly49T), were localised in the new reference genomes. We conducted the first genome-wide scan of variable number tandem repeats (VNTRs) within the coding regions of mice, identifying over 400 genes with VNTR polymorphisms up to more than 600 repeat copies and repeat units reaching 990 nucleotides. Our strain-specific annotations enhance RNA-Seq analyses, as demonstrated in PWK/PhJ, where we observed a 5.1% improvement in read mapping and expression level differences in 2.1% of coding genes compared to using GRCm39.

genomics↗