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Vader, L.

Publications and source records attributed to Vader, L..

3 recordsLinked to original sources

geneML: Gene annotation across diverse fungal species using deep learning

Accurate gene prediction remains a major bottleneck in fungal genomics, where lineage diversity and alternative splicing challenge existing ab initio methods. Here, we present geneML, a deep learning-based gene prediction tool tailored to fungal genomes. Across nine reference genomes spanning diverse fungal taxa, geneML improved gene-level F1 score from 64.9 to 67.1 compared to BRAKER3 with protein-based hints, driven by substantially higher recall (69.0 vs. 64.1) at equivalent precision. geneML also remains fast, averaging around 6 minutes per genome on a standard 8-core CPU. A key feature of geneML is its ability to predict alternative transcripts. Compared to Fusarium graminearum Iso-Seq control data, it achieves 41.1% transcript recall and 71.1% precision, outperforming AUGUSTUS (33.8% recall, 48.9% precision), one of the few tools that support isoform prediction. The predicted transcript diversity is consistent with experimentally observed fungal alternative splicing patterns. Reannotation of the curated training dataset further suggests improved biological completeness, with geneML recovering 15.3% more genes containing complete PFAM domains than the reference annotation. These results demonstrate that geneML enables faster, more sensitive, and more biologically informative fungal genome annotation. geneML is available as an open-source command-line tool at https://github.com/hexagonbio/geneML. Key Points- geneML improves gene prediction accuracy over both classical and recent deep learning-based methods, while substantially improving recall. - geneML predicts alternative transcripts with higher precision and recall than AUGUSTUS, expanding functional annotation. - Runtime was 32-fold decreased over BRAKER3, enabling efficient high-throughput genome annotation. - geneML identifies novel genes and recovers missing annotations, especially in under-annotated non-Ascomycete genomes.

bioinformatics↗

PhyloNaP: a user-friendly database of Phylogeny for Natural Product-producing enzymes

Phylogenetic analysis is widely used to predict enzyme function, yet building annotated and reusable trees is labor-intensive and requires extensive knowledge about the specific enzymes. Existing resources rarely cover biosynthetic enzymes and lack the context needed for meaningful analysis. We present PhyloNaP, the first large-scale resource dedicated to phylogenies of biosynthetic enzymes. PhyloNaP provides [~]18,500 annotated and interactive trees enriched with chemical, functional, and taxonomic information. Users can classify their own sequences via phylogenetic placement, enabling functional inference in an evolutionary context. A contribution portal allows the community to submit curated trees. By combining scale, breadth of annotation, and interactive functionality, PhyloNaP fills a major gap in bioinformatics resources for enzyme discovery and annotation, with immediate applications to secondary metabolism and beyond. Availabilityhttps://phylonap.cs.uni-tuebingen.de

bioinformatics↗

PlasmidEC and gplas2: An optimised short-read approach to predict and reconstruct antibiotic resistance plasmids in Escherichia coli

Accurate reconstruction of Escherichia coli antibiotic resistance gene (ARG) plasmids from Illumina sequencing data has proven to be a challenge with current bioinformatic tools. In this work, we present an improved method to reconstruct E. coli plasmids using short reads. We developed plasmidEC, an ensemble classifier that identifies plasmid-derived contigs by combining the output of three different binary classification tools. We showed that plasmidEC is especially suited to classify contigs derived from ARG plasmids with a high recall of 0.941. Additionally, we optimised gplas, a graph-based tool that bins plasmid-predicted contigs into distinct plasmid predictions. Gplas2 is more effective at recovering plasmids with large sequencing coverage variations and can be combined with the output of any binary classifier. The combination of plasmidEC with gplas2 showed a high completeness (median=0.818) and F1-score (median=0.812) when reconstructing ARG plasmids and exceeded the binning capacity of the reference-based method MOB-suite. In the absence of long read data, our method offers an excellent alternative to reconstruct ARG plasmids in E. coli. Data SummaryNo new sequencing data have been generated in this study. All genomes used in this research are publicly available at the GenBank and Sequence Read Archive of the National Center for Biotechnology Information. Accession numbers are specified in Supplementary Materials. Scripts to reproduce the results reported in this manuscript can be accessed at https://gitlab.com/jpaganini/ecoli-binary-classifier. The ensemble classifier, plasmidEC, is publicly available at https://gitlab.com/mmb-umcu/plasmidEC (release 1.3.1), and gplas2 (release 1.0.0) can be found at https://gitlab.com/mmb-umcu/gplas2. Impact StatementEscherichia coli has emerged as a highly pervasive multidrug resistant pathogen on a global scale. The dissemination of resistance is significantly influenced by plasmids, mobile genetic elements that facilitate the transfer of antimicrobial resistance genes within and between diverse bacterial species. Consequently, precise and high-throughput identification of plasmids is imperative for effective genomic surveillance of resistance. However, accurate plasmid reconstruction remains challenging with the use of affordable short-read sequencing data. In this work, we present a novel method to accurately predict and reconstruct E. coli plasmids based on Illumina data. Additionally, we demonstrate that our approach outperforms the reference-based method MOB-suite, especially when reconstructing plasmids carrying antimicrobial resistance genes.

bioinformatics↗