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

Timofey Prodanov

Düsseldorf University Hospital

ORCID: 0000-0001-7469-6651

Also affiliated with Heinrich Heine University Düsseldorf

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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 2%percentile
3.1Author DataRank

Indexed papers

3in 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 3 indexed papers 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.

Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.18.590093
Top 16%
1.3DataRank
Top 16%38 citations

Samarendra Pani, Bernardo Rodríguez–Martín, Jana Ebler, Carsten Hain, Vasiliki Tsapalou +10 more

Papers

Driven by 11 papers — median percentile 81. Top paper: “Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project”.

Long-read sequencing and structural variant characterization in 1,019 samples from the 1000 Genomes Project

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.18.590093
Top 16%
1.3DataRank
Top 16%38 citations

Samarendra Pani, Bernardo Rodríguez–Martín, Jana Ebler, Carsten Hain, Vasiliki Tsapalou +10 more

Complex genetic variation in nearly complete human genomes

Nature(2025)10.1038/s41586-025-09140-6
Top 19%
1.1DataRank
Top 19%83 citations

Peter Ebert, Peter A. Audano, Mark Loftus, David Porubsky, Feyza Yilmaz +62 more

Complex genetic variation in nearly complete human genomes

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.24.614721
Top 27%
0.741DataRank
Top 27%27 citations

Peter Ebert, Peter A. Audano, Mark Loftus, David Porubsky, Feyza Yilmaz +62 more

Structural and genetic diversity in the secreted mucins MUC5AC and MUC5B

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.06.007
N/A
0.627DataRank · unranked
22 citations

Timofey Prodanov, PingHsun Hsieh, Evangelos Nizamis, William T. Harvey, Arvis Sulovari +8 more

Impact and characterization of serial structural variations across humans and great apes

Nature Communications(2024)10.1038/s41467-024-52027-9
N/A
0.385DataRank · unranked
12 citations

Tobias Rausch, Michael Jendrusch, Hufsah Ashraf, Peter A. Audano, Ola Austine +49 more

A multilocus approach for accurate variant calling in low-copy repeats using whole-genome sequencing

Bioinformatics(2023)10.1093/bioinformatics/btad268
N/A
0DataRank · unranked
2 citations

Vikas Bansal, Timofey Prodanov

Sensitive alignment using paralogous sequence variants improves long read mapping and variant calling in segmental duplications

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.15.202929
N/A
0DataRank · unranked
3 citations

Vikas Bansal, Timofey Prodanov

Structural and genetic diversity in the secreted mucins, MUC5AC and MUC5B

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.03.18.585560
N/A
0DataRank · unranked
0 citations

Timofey Prodanov, PingHsun Hsieh, Evangelos Nizamis, William T. Harvey, Arvis Sulovari +8 more

Structural variation in 1,019 diverse humans based on long-read sequencing

Nature(2025)10.1038/s41586-025-09290-7
N/A
0DataRank · unranked
56 citations

Samarendra Pani, Jana Ebler, Carsten Hain, Vasiliki Tsapalou, Arda Soylev +27 more

Locityper enables targeted genotyping of complex polymorphic genes

Nature Genetics(2025)10.1038/s41588-025-02362-4
N/A
0DataRank · unranked
9 citations

Elizabeth G. Plender, Guiscard Seebohm, Sven G. Meuth, Evan E. Eichler, Tobias Marschall +1 more

Sequence-to-graph alignment based copy number calling using a network flow formulation

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.11.21.689771
N/A
0DataRank · unranked
0 citations

Jonas Weber, Gunnar W. Klau, Tobias Marschall, Timofey Prodanov, Hugo Magalhães