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

Andreas Scherer

Institute for Molecular Medicine Finland

ORCID: 0000-0002-4254-7122
Biochemistry, Genetics and Molecular BiologyMedicine

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
5.7Author 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.

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Nature Biotechnology(2021)10.1038/s41587-021-00993-6
Top 8%
2.7DataRank
Top 8%153 citations

Bin Zhu, Yongmei Zhao, Wanqiu Chen, Zhaowei Yang, Liz Kerrigan +88 more

Papers

Driven by 11 papers — median percentile 80. Top paper: “Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing”.

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing

Nature Biotechnology(2021)10.1038/s41587-021-00994-5
N/A
3.8DataRank · unranked
215 citations

Luyao Ren, Zhong Chen, Li Tai Fang, Yongmei Zhao, Justin Lack +85 more

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Nature Biotechnology(2021)10.1038/s41587-021-00993-6
Top 8%
2.7DataRank
Top 8%153 citations

Bin Zhu, Yongmei Zhao, Wanqiu Chen, Zhaowei Yang, Liz Kerrigan +88 more

Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study

Scientific Data(2021)10.1038/s41597-021-01077-5
Top 12%
1.7DataRank
Top 12%60 citations

Li Tai Fang, Tsai-Wei Shen, Sulbha Choudhari, Keyur Talsania, Xiongfong Chen +33 more

Reporting guidelines for human microbiome research: the STORMS checklist

Nature Medicine(2021)10.1038/s41591-021-01552-x
N/A
0.918DataRank · unranked
454 citations

Audrey Renson, Genomic Standards Consortium, Cesare Furlanello, Shaimaa Elsafoury, Ludwig Geistlinger +98 more

Quartet RNA reference materials improve the quality of transcriptomic data through ratio-based profiling

Nature Biotechnology(2023)10.1038/s41587-023-01867-9
Top 28%
0.709DataRank
Top 28%41 citations

Wanwan Hou, Yaqing Liu, Haiyan Wang, Lianhua Dong, Yuanbang Mai +44 more

Whole Genome and Exome Sequencing Reference Datasets from A Multi-center and Cross-platform Benchmark Study

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.27.433136
Top 33%
0.603DataRank
Top 33%10 citations

Li Tai Fang, Tsai-Wei Shen, Sulbha Choudhari, Keyur Talsania, Xiongfong Chen +31 more

Augmenting precision medicine via targeted RNA-Seq detection of expressed mutations

npj Precision Oncology(2025)10.1038/s41698-025-00993-8
N/A
0DataRank · unranked
5 citations

Jianying Li, Donald J. Johann, Daniel Butler, Guangchun Chen, Jonathan Foox +20 more

Evaluating the analytical validity of circulating tumor DNA sequencing assays for precision oncology

Nature Biotechnology(2021)10.1038/s41587-021-00857-z
N/A
0DataRank · unranked
271 citations

Binsheng Gong, Kevin Lai, Jennifer S. LoCoco, Todd Richmond, Jeoffrey Schageman +82 more

A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency

Genome biology(2021)10.1186/s13059-021-02316-z
N/A
0DataRank · unranked
61 citations

Binsheng Gong, Natalia Novoradovskaya, Dan Li, Rebecca Kusko, Todd Richmond +69 more

The SEQC2 epigenomics quality control (EpiQC) study

Genome biology(2021)10.1186/s13059-021-02529-2
N/A
0DataRank · unranked
60 citations

Jessica Nordlund, Claudia Lalancette, Ting Gong, Michelle Lacey, Samantha Lent +52 more

Assessing reproducibility of inherited variants detected with short-read whole genome sequencing

Genome biology(2022)10.1186/s13059-021-02569-8
N/A
0DataRank · unranked
56 citations

Luyao Ren, Vitor Onuchic, Meijian Guan, Rebecca Kusko, Steve Bruinsma +50 more