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

Jana Ebler

Research Institute of Molecular Pathology

ORCID: 0000-0002-0382-3702

Also affiliated with Düsseldorf University Hospital, 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 1%percentile
13.2Author DataRank

Indexed papers

6in 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 6 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.

Haplotype-resolved diverse human genomes and integrated analysis of structural variation

Science(2021)10.1126/science.abf7117
Top 4%
5.7DataRank
Top 4%812 citations

Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubsky, Marc Jan Bonder +60 more

Papers

Driven by 21 papers — median percentile 68. Top paper: “Haplotype-resolved diverse human genomes and integrated analysis of structural variation”.

Haplotype-resolved diverse human genomes and integrated analysis of structural variation

Science(2021)10.1126/science.abf7117
Top 4%
5.7DataRank
Top 4%812 citations

Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubsky, Marc Jan Bonder +60 more

A draft human pangenome reference

Nature(2023)10.1038/s41586-023-05896-x
Top 4%
5.1DataRank
Top 4%1169 citations

Mobin Asri, Jana Ebler, Daniel Doerr, Marina Haukness, Hickey, Glenn +95 more

Pangenome graph construction from genome alignments with Minigraph-Cactus

Nature Biotechnology(2023)10.1038/s41587-023-01793-w
N/A
5.0DataRank · unranked
318 citations

Jean Monlong, Jana Ebler, Adam M. Novak, Jordan M. Eizenga, Yan Gao +94 more

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

A strategy for building and using a human reference pangenome

F1000Research(2021)10.12688/f1000research.19630.2
N/A
0.533DataRank · unranked
10 citations

Giuseppe Narzisi, Valérie Schneider, Peter A. Audano, Evan Biederstedt, Lon Blauvelt +35 more

SVarp: pangenome-based structural variant discovery

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.18.580171
Top 48%
0.378DataRank
Top 48%8 citations

Jana Ebler, Samarendra Pani, Tobias Rausch, Jan O. Korbel, Tobias Marschall +1 more

Pan-conserved segment tags identify ultra-conserved sequences across assemblies in the human pangenome

Cell Reports Methods(2023)10.1016/j.crmeth.2023.100543
Top 50%
0.352DataRank
Top 50%6 citations

Stephanie Greer, Dmitri S. Pavlichin, Bo Zhou, Alexander E. Urban, Tsachy Weissman +94 more

De novo assembly of 64 haplotype-resolved human genomes of diverse ancestry and integrated analysis of structural variation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.16.423102
Top 53%
0.322DataRank
Top 53%5 citations

Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubsky, Marc Jan Bonder +58 more

Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall

Genome Research(2023)10.1101/gr.278070.123
N/A
0DataRank · unranked
36 citations

Peter Ebert, Jana Ebler, Peter A. Audano, Katherine M. Munson, Kendra Hoekzema +6 more

Whole-genome long-read sequencing downsampling and its effect on variant calling precision and recall

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.04.539448
N/A
0DataRank · unranked
11 citations

Peter Ebert, Jana Ebler, Peter A. Audano, Katherine M. Munson, Kendra Hoekzema +6 more

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

Nature Communications(2024)10.1038/s41467-024-52027-9
N/A
0DataRank · unranked
12 citations

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

Pangenome Graphs

Annual Review of Genomics and Human Genetics(2020)10.1146/annurev-genom-120219-080406
N/A
0DataRank · unranked
355 citations

Adam M. Novak, Jonas A. Sibbesen, Simon Heumos, Ali Ghaffaari, Hickey, Glenn +11 more

Structural and transduction patterns of human-specific polymorphic SVA insertions

Mobile DNA(2025)10.1186/s13100-025-00373-w
N/A
0DataRank · unranked
1 citations

Mark Loftus, Emily C. Golba, Haley Abel, Hufsah Ashraf, Peter A. Audano +64 more

Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads

Nature Biotechnology(2020)10.1038/s41587-020-0719-5
N/A
0DataRank · unranked
228 citations

Peter Ebert, Peter A. Audano, Mitchell R. Vollger, William T. Harvey, Pierre Marijon +16 more

Pangenome-based genome inference

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.11.378133
N/A
0DataRank · unranked
25 citations

Wayne E. Clarke, Tobias Rausch, Peter A. Audano, Torsten Houwaart, Jan O. Korbel +5 more

Haplotype-resolved inversion landscape reveals hotspots of mutational recurrence associated with genomic disorders

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.20.472354
N/A
0DataRank · unranked
11 citations

Wolfram Höps, Hufsah Ashraf, PingHsun Hsieh, Bernardo Rodríguez–Martín, Feyza Yilmaz +20 more

Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes

Nature Genetics(2022)10.1038/s41588-022-01043-w
N/A
0DataRank · unranked
290 citations

Peter Ebert, Wayne E. Clarke, Tobias Rausch, Peter A. Audano, Torsten Houwaart +7 more

Inversion polymorphism in a complete human genome assembly

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.06.511148
N/A
0DataRank · unranked
5 citations

William T. Harvey, Allison N. Rozanski, Jana Ebler, Wolfram Höps, Hufsah Ashraf +7 more

Inversion polymorphism in a complete human genome assembly

Genome biology(2023)10.1186/s13059-023-02919-8
N/A
0DataRank · unranked
33 citations

William T. Harvey, Allison N. Rozanski, Jana Ebler, Wolfram Höps, Hufsah Ashraf +7 more

Allele detection using k-mer-based sequencing error profiles

Bioinformatics Advances(2023)10.1093/bioadv/vbad149
N/A
0DataRank · unranked
1 citations

Jana Ebler, Tobias Marschall, Hufsah Ashraf