Author

Matteo Tommaso Ungaro

Sapienza University of RomeORCID 0000-0002-1107-3307Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Research Focus:genome assembly· 1

Frequent Co-Authors

Adam M. NovakiD· 1 shared Alessandro RosaiD· 1 shared Alexander G. IoannidisiD· 1 shared Andrea Tanzer AiD· 1 shared Andrew W. CarrolliD· 1 shared Benedict PateniD· 1 shared Elena Di TommasoiD· 1 shared Erich David JarvisiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperBioinformatics

Adam M. NovakORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintMar 30, 2026

The diploid reference genome of a human embryonic stem cell line

Ivana Pačar, Matteo Tommaso Ungaro, Ying Chen…·Simona Giunta

The paper presents the first telomere-to-telomere diploid reference genome of the human embryonic stem cell line H9, revealing genomic features and ancestry.

1 citation

humanwhole-genome sequencing

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BioinformaticsNature MethodsPeer-reviewedSep 11, 2024

Personalized Pangenome References

Jouni Sirén, Parsa Eskandar, Matteo Tommaso Ungaro…·Benedict Paten

The paper introduces a personalized pangenome approach to improve short-read mapping and variant calling by reducing reference bias and errors.

40 citationstop 2%

humanwhole-genome sequencing

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