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Rauschning, L.

Publications and source records attributed to Rauschning, L..

2 recordsLinked to original sources

Binary node clustering via contrastive learning for haplotype phasing in de novo genome assembly

Accurate haplotype phasing is essential for high-quality genome assembly, yet de novo phasing of complex genomes without parental data remains challenging. We formulate haplotype phasing as a node clustering problem with overlapping clusters on augmented unitig graphs, where nodes represent contiguous, non-branching DNA sequence fragments and two edge types can encode sequence overlap or Hi-C proximity information. We introduce a contrastive learning framework with a custom objective function and train a graph-transformer-based model, termed grapHiC, to phase paternal, maternal, and homozygous unitig nodes. grapHiC; is the first machine-learning-based method to perform reference-free haplotype phasing and the first approach to directly phase raw unitig graphs without prior simplification. We show that grapHiCaccurately clusters nodes on human-genome-scale graphs and that its predictions can effectively guide phased de novo genome assembly, producing human assemblies with contiguity and phasing quality comparable to the state of the art when integrated with the DipGNNome assembler.

bioinformatics↗

An nf-core framework for the systematic comparison of alternative modeling tools: the multiple sequence alignment case study

The computational complexity of many key bioinformatics problems has resulted in numerous alternative heuristic solutions, where no single approach consistently outperforms all others. This creates difficulties for users trying to identify the most suitable tool for their dataset and for developers managing and evaluating alternative methods. As data volumes grow, deploying these methods becomes increasingly difficult, highlighting the need for standardized frameworks for seamless tool deployment and comparison in HPC environments. Multiple sequence aligners (MSAs) rank among the most commonly employed modeling techniques in bioinformatics, playing a crucial role in applications such as protein structure prediction, phylogenetic reconstruction, and variant effect prediction. The NP-hardness of MSAs makes them a major example of problems where heuristics stand central, as no optimal solution can be currently obtained, within the limits of operational computational requirements. Here, we present a pilot design of an nf-core framework for streamlined tool deployment and rigorous performance evaluation focusing on the MSAs software ecosystem. By integrating the most popular MSA tools and focusing on a modular, and extensible architecture, we aspire to provide a key platform supporting MSA deployment, evaluation, and algorithmics development to the MSA community, and a proof-of-principle to the wider bioinformatics community.

bioinformatics↗