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

Álvaro Martínez Barrio

Uppsala University

ORCID: 0000-0001-5064-2093

Also affiliated with Science for Life Laboratory, European Space Agency, TiGenix (Spain)

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological SciencesImmunology and Microbiology

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
8.9Author 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.

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 6 papers — median percentile 89. Top paper: “A robust benchmark for detection of germline large deletions and insertions”.

A robust benchmark for detection of germline large deletions and insertions

Nature Biotechnology(2020)10.1038/s41587-020-0538-8
N/A
10.3DataRank · unranked
486 citations

Nancy F. Hansen, Nathan D. Olson, Lesley M. Chapman, James C. Mullikin, Chunlin Xiao +45 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

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

Linking T cell receptor sequence to transcriptional profiles with clonotype neighbor graph analysis (CoNGA)

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.04.134536
N/A
0DataRank · unranked
13 citations

Kate Manley, Jeremy Chase Crawford, Aisha Souquette, Álvaro Martínez Barrio, Michael J. T. Stubbington +3 more

Integrating T cell receptor sequences and transcriptional profiles by clonotype neighbor graph analysis (CoNGA)

Nature Biotechnology(2021)10.1038/s41587-021-00989-2
N/A
0DataRank · unranked
136 citations

Kate Manley, Jeremy Chase Crawford, Aisha Souquette, Álvaro Martínez Barrio, Michael J. T. Stubbington +3 more