News
Characterizing influenza A virus lineages and clinically relevant mutations through high-coverage wastewater sequencing
We’re happy to announce our study on tracing influenza A from wastewater. We developed a novel tiling amplicon approach, enabling deep genomic coverage of influenza A. The method allows for robust identification of circulating influenza A clades as well as vaccine-site and drug-target mutations, generating data that can inform public health interventions. Our method is now part of nationwide wastewater surveillance efforts: https://www.sciencedirect.com/science/article/pii/S0043135425013570 .
Estimated transmission dynamics of SARS-CoV-2 variants from wastewater are unbiased and robust to differential shedding
Wastewater-based epidemiology avoids many biases of clinical testing but can potentially have its own. Using mathematical modelling, simulations, and Swiss data, we show that pathogen shedding, even when differing between genomic variants, does not bias key metrics such as selection advantage, supporting wastewater monitoring as a reliable tool for continued surveillance: https://www.nature.com/articles/s41467-025-62790-y.
Phylogenetic inference reveals clonal heterogeneity in circulating tumor cell clusters
We are excited to share our latest research published in Nature Genetics, where we could detect genetic heterogeneity within circulating tumor cell clusters that can seed metastases. To do so, we tailor-made a new phylogenetic algorithm "CTC-SCITE": https://www.nature.com/articles/s41588-025-02205-2
VILOCA: sequencing quality-aware viral haplotype reconstruction and mutation calling for short-read and long-read data
We are excited to share that our new tool VILOCA has been published! VILOCA is a novel method for mutation calling and local haplotype reconstruction from diverse viral short-read and long-read sequencing data. It has already proven to be useful in various settings, including classical mutation calling for single or longitudinal samples, and viral surveillance in wastewater. You can check out our published paper in NAR Genomics and Bioinformatics: https://doi.org/10.1093/nargab/lqae152