🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Michele Berselli

Harvard University

ORCID: 0000-0001-8577-9137
Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 7%percentile
0.165Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

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

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.681545
Top 70%
0.165DataRank
Top 70%2 citations

Dominika Maziec, Julia Markowski, Stephanie Georges, Nancy L. Parmalee, Michele Berselli +41 more

Papers

Driven by 7 papers — median percentile 30. Top paper: “Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations”.

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2
N/A
0.269DataRank · unranked
5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.681545
Top 70%
0.165DataRank
Top 70%2 citations

Dominika Maziec, Julia Markowski, Stephanie Georges, Nancy L. Parmalee, Michele Berselli +41 more

Chromoscope: interactive multiscale visualization for structural variation in human genomes

OSF Preprints (OSF Preprints)(2023)10.31219/osf.io/pyqrx
N/A
0DataRank · unranked
1 citations

Dominika Maziec, Victoria L. Stevens, Trevor Manz, Alexander Veit, Michele Berselli +4 more

BamSnap: a lightweight viewer for sequencing reads in BAM files

Bioinformatics(2020)10.1093/bioinformatics/btaa1101
N/A
0DataRank · unranked
17 citations

Soohyun Lee, Michele Berselli, Chong Chu, Peter J. Park, Min‐Seok Kwon

Comprehensive benchmarking of somatic structural variant detection at ultra-low allele fractions

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.18.677206
N/A
0DataRank · unranked
5 citations

Adam C. English, Luis F. Paulin, Christopher M. Grochowski, Surabhi Maheshwari, Taralynn Mack +7 more

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.13.580158
N/A
0DataRank · unranked
3 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +14 more

Chromoscope: interactive multiscale visualization for structural variation in human genomes

Nature Methods(2023)10.1038/s41592-023-02056-x
N/A
0DataRank · unranked
7 citations

Dominika Maziec, Victoria Stevens, Trevor Manz, Alexander Veit, Michele Berselli +4 more