Péter Kómár

This paper introduces a graph genome reference that improves read alignment and variant calling accuracy compared to traditional haplotype-based methods.

This paper introduces VBT, a tool for identifying Mendelian violations in family trios by solving the 3-way variant matching problem, showing improved accuracy over existing methods.

The paper introduces a statistical model to benchmark variant calling pipelines using trio data, showing it can estimate precision and recall differences with low uncertainty.