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

Wayne E. Clarke

Golder Associates (Canada)

ORCID: 0000-0003-2471-0712

Also affiliated with Saskatchewan Health Authority, New York Genome Center

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
34.0Author DataRank

Indexed papers

9in 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 9 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.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y
Top 3%
7.0DataRank
Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 14 papers — median percentile 96. Top paper: “Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program”.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y
Top 3%
7.0DataRank
Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

Cell(2022)10.1016/j.cell.2022.08.004
Top 3%
6.3DataRank
Top 3%1056 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +37 more

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

High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.06.430068
Top 4%
5.5DataRank
Top 4%260 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +16 more

Benchmarking challenging small variants with linked and long reads

Cell Genomics(2022)10.1016/j.xgen.2022.100128
Top 4%
4.9DataRank
Top 4%212 citations

Nathan D. Olson, Lindsay Harris, Ziad Khan, Jesse Farek, Medhat Mahmoud +36 more

Benchmarking challenging small variants with linked and long reads

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.24.212712
Top 11%
2.0DataRank
Top 11%60 citations

Nathan D. Olson, Lindsay Harris, Jennifer McDaniel, Ziad Khan, Jesse Farek +37 more

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

Genome Research(2024)10.1101/gr.279273.124
Top 13%
1.7DataRank
Top 13%78 citations

Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe +42 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

A crowdsourced set of curated structural variants for the human genome

PLoS Computational Biology(2020)10.1371/journal.pcbi.1007933
Top 40%
0.482DataRank
Top 40%14 citations

Noah Spies, Patrick Pai, Chun Shen Lim, Andrew Carroll, Giuseppe Narzisi +19 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

taxMaps - Ultra-comprehensive and highly accurate taxonomic classification of short-read data in reasonable time

bioRxiv (Cold Spring Harbor Laboratory)(2017)10.1101/134023
N/A
0.241DataRank · unranked
4 citations

Wayne E. Clarke, Nicolas Robine, Michael C. Zody, André Corvelo

Structural and transduction patterns of human-specific polymorphic SVA insertions

Mobile DNA(2025)10.1186/s13100-025-00373-w
N/A
0.104DataRank · unranked
1 citations

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

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