Mojca Stražišar

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions

A signal processing and deep learning framework for methylation detection using Oxford Nanopore sequencing

Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome

Genetic variants in microRNA genes: impact on microRNA expression, function, and disease