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

William J. Rowell

Pacific Biosciences (United States)

ORCID: 0000-0002-7422-1194
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 1%percentile
9.3Author DataRank

Indexed papers

4in 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 4 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.

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

Papers

Driven by 11 papers — median percentile 89. Top paper: “Benchmarking challenging small variants with linked and long reads”.

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

A diploid assembly-based benchmark for variants in the major histocompatibility complex

Nature Communications(2020)10.1038/s41467-020-18564-9
Top 11%
2.0DataRank
Top 11%102 citations

Justin Wagner, Qiandong Zeng, Erik Garrison, Shilpa Garg, Arkarachai Fungtammasan +21 more

Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

Nature Biotechnology(2019)10.1038/s41587-019-0217-9
N/A
1.1DataRank · unranked
1912 citations

Paul Peluso, William J. Rowell, Pi-Chuan Chang, Richard J. Hall, Gregory T. Concepcion +24 more

The Platinum Pedigree: A long-read benchmark for genetic variants

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.10.02.616333
Top 53%
0.321DataRank
Top 53%6 citations

C. Nolan, Tom Mokveld, William J. Rowell, S. Y. Lee, Egor Dolzhenko +26 more

A population of descending neurons that regulate the flight motor of Drosophila

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.05.455281
N/A
0DataRank · unranked
1 citations

Ivo G. Ros, Carmen Morrow, William J. Rowell, Gwyneth M Card, Wyatt Korff +2 more

A population of descending neurons that regulates the flight motor of Drosophila

Current Biology(2022)10.1016/j.cub.2022.01.008
N/A
0DataRank · unranked
81 citations

Ivo G. Ros, Carmen Morrow, William J. Rowell, Gwyneth M Card, Wyatt Korff +2 more

Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy

medRxiv(2021)10.1101/2021.12.06.21264306
N/A
0DataRank · unranked
1 citations

Teddi Gray, Meghan C. Campbell, Jenny Ekholm, Aaron M. Wenger, William J. Rowell +7 more

Characterization and visualization of tandem repeats at genome scale

Nature Biotechnology(2024)10.1038/s41587-023-02057-3
N/A
0DataRank · unranked
128 citations

Adam C. English, Harriet Dashnow, Guilherme De Sena Brandine, Tom Mokveld, William J. Rowell +18 more

Identification of de novo variants from parent-proband duos via long-read sequencing

medRxiv(2025)10.1101/2025.02.24.25322424
N/A
0DataRank · unranked
0 citations

Emmanuèle C. Délot, Georgia Pitsava, Christine Lambert, Cairbre Fanslow, Primo Baybayan +12 more

Germline mosaicism of a missense variant in KCNC2 in a multiplex family with autism and epilepsy characterized by long‐read sequencing

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62743
N/A
0DataRank · unranked
13 citations

Teddi Gray, Meghan C. Campbell, Jenny Ekholm, Aaron M. Wenger, William J. Rowell +7 more