- wenda_gpu: fast domain adaptation for genomic data
- WMSA: a novel method for multiple sequence alignment of DNA sequences
- GeneNetTools: Tests for Gaussian graphical models with shrinkage
- GBZ File Format for Pangenome Graphs
- Integrating Phylogenetic and Functional Data in Microbiome Studies
- CITEdb: a manually curated database of cell-cell interactions in human
- Top-Down Crawl: A method for the ultra-rapid and motif-free alignment of sequences with associated binding metrics
- mHapTk: A comprehensive toolkit for the analysis of DNA methylation haplotypes
- SpaceX: Gene Co-expression Network Estimation for Spatial Transcriptomics
- SCAFE: a software suite for analysis of transcribed cis-regulatory elements in single cells
- Homologue Series Detection and Management in LC-MS data with homologueDiscoverer
- Correction to: Integrative data semantics through a model-enabled data stewardship
- Computational modelling in health and disease: highlights of the 6th annual SysMod meeting
- Predicting colorectal cancer tumor mutational burden from histopathological images and clinical information using multi-modal deep learning
- BioBulkFoundary: A customized webserver for exploring biosynthetic potentials of bulk chemicals
- Increasing confidence in proteomic spectral deconvolution through mass defect
- Highly significant improvement of protein sequence alignments with AlphaFold2
- Lung Cancer Subtype Diagnosis using Weakly-paired Multi-omics Data
- Reproducible acquisition, management, and meta-analysis of nucleotide sequence (meta)data using q2-fondue
- CGV: Cancer Genome Viewer, a web service for integrative cancer genome and pharmacogenomic data analysis