Marcin Kierczak

The paper decomposes polygenic risk of coronary artery disease into distinct biological processes using latent factor decomposition of genetic variants.

GenErode provides a pipeline to analyze genomic erosion by comparing ancient and modern whole-genome re-sequencing data, producing standardized erosion indices.

This study uses linked-read whole-genome sequencing to detect structural variants and copy number variations in multiple myeloma, identifying both common and private variants that affect gene regulation and molecular classification.

The paper introduces a novel single nuclei sequencing and assembly workflow to generate reference genomes from arbuscular mycorrhizal fungi, bypassing the need for culturing.

HaploDistScan detects genomic regions of deep divergence using haplotype distances without prior population information, identifying balancing selection in ruff and Darwin's finch data.