Author

Dominika Maziec

Harvard UniversityORCID 0009-0009-4427-7267Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Organism:human· 1

Frequent Co-Authors

Hu JiniD· 2 shared Peter J. ParkiD· 2 shared Alexander D. VeitiD· 1 shared Alexi M. RunnelsiD· 1 shared Andrew B. StergachisiD· 1 shared Azeet NarayaniD· 1 shared Benpeng MiaoiD· 1 shared Beverly J. FuiD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenomics

Hu JinORCID

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2 papers

Recent·Most cited

GenomicsGenome biologyPeer-reviewedApr 17, 2026

A recurrent sequencing artifact on Illumina sequencers with two-color fluorescent dye chemistry and its impact on somatic variant detection

Beverly J. Fu, Vinay Viswanadham, Dominika Maziec…·Peter J. Park

The paper identifies a sequencing artifact in Illumina NovaSeq 6000 two-color chemistry that causes T>G substitutions, affecting low-VAF somatic variant detection.

1 citation

whole-genome sequencingstatistical model

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BioinformaticsbioRxivPreprintOct 13, 2025

Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data

Yoo-Jin Jiny Ha, Dominika Maziec, Julia Markowski…·Peter J. Park

The paper benchmarks somatic variant and indel detection at low allele fractions using short- and long-read data, finding sensitivity and precision around 80% at 300x coverage.

3 citations

humanwhole-genome sequencing

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