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

Sairam Behera

Central Research Institute for Dryland Agriculture

ORCID: 0000-0002-9047-0203

Also affiliated with Baylor College of Medicine, The University of Texas Health Science Center at Houston

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 4%percentile
0.629Author DataRank

Indexed papers

2in 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 2 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.

Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

Scientific Data(2025)10.1038/s41597-025-05438-2
Top 44%
0.421DataRank
Top 44%10 citations

Vaidehi Patel, Nathan D. Olson, Hua‐Jun He, Anthony Schmitt, Kenneth D. Cole +80 more

Papers

Driven by 21 papers — median percentile 46. Top paper: “Beyond the exome: What’s next in diagnostic testing for Mendelian conditions”.

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009
N/A
2.2DataRank · unranked
123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 more

Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

Scientific Data(2025)10.1038/s41597-025-05438-2
Top 44%
0.421DataRank
Top 44%10 citations

Vaidehi Patel, Nathan D. Olson, Hua‐Jun He, Anthony Schmitt, Kenneth D. Cole +80 more

Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.24.538128
N/A
0.406DataRank · unranked
14 citations

Jonathan R. Belyeu, Xiao Chen, Luis F. Paulin, Ngoc Quynh Nguyen, E. Newman +21 more

Fixing reference errors efficiently improves sequencing results

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.07.18.500506
Top 65%
0.208DataRank
Top 65%3 citations

Jonathon LeFaive, Peter Orchard, Medhat Mahmoud, Luis F. Paulin, Jesse Farek +7 more

Multiscale Analysis of Pangenome Enables Improved Representation of Genomic Diversity For Repetitive And Clinically Relevant Genes

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.05.502980
N/A
0DataRank · unranked
5 citations

Sairam Behera, Asif Khalak, Fritz J. Sedlazeck, Justin Wagner, Justin M. Zook +1 more

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

Nature Methods(2023)10.1038/s41592-023-01993-x
N/A
0DataRank · unranked
143 citations

Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach +25 more

Comprehensive Structural Variant Detection: From Mosaic to Population-Level

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.04.487055
N/A
0DataRank · unranked
97 citations

Luis F. Paulin, Christopher M. Grochowski, Dominic W. Horner, Medhat Mahmoud, Sairam Behera +9 more

FixItFelix: improving genomic analysis by fixing reference errors

Genome biology(2023)10.1186/s13059-023-02863-7
N/A
0DataRank · unranked
27 citations

Jonathon LeFaive, Peter Orchard, Medhat Mahmoud, Luis F. Paulin, Jesse Farek +7 more

Scalable Nanopore sequencing of human genomes provides a comprehensive view of haplotype-resolved variation and methylation

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.12.523790
N/A
0DataRank · unranked
31 citations

Kimberley J. Billingsley, Mira Mastoras, Melissa Meredith, Jean Monlong, Ryan Lorig-Roach +25 more

An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates

F1000Research(2021)10.12688/f1000research.51477.1
N/A
0DataRank · unranked
3 citations

Medhat Mahmoud, Michael D. Jochum, Daniel Paiva Agustinho, Barry Zorman, Ahmad Al Khleifat +57 more

Single-cell somatic copy number variants in brain using different amplification methods and reference genomes

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.07.552289
N/A
0DataRank · unranked
2 citations

Zeliha Gözde Turan, Diego Pérez‐Rodríguez, Ida Bomann, Sairam Behera, Caoimhe Morley +6 more

Detection of mosaic and population-level structural variants with Sniffles2

Nature Biotechnology(2024)10.1038/s41587-023-02024-y
N/A
0DataRank · unranked
448 citations

Luis F. Paulin, Christopher M. Grochowski, Dominic W. Horner, Medhat Mahmoud, Sairam Behera +9 more

Comprehensive genome analysis and variant detection at scale using DRAGEN

Nature Biotechnology(2024)10.1038/s41587-024-02382-1
N/A
0DataRank · unranked
110 citations

Severine Catreux, Massimiliano Rossi, Sean Truong, Zhuoyi Huang, Michael Ruehle +12 more

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Genetics in Medicine(2024)10.1016/j.gim.2024.101199
N/A
0DataRank · unranked
14 citations

Seth Berger, Samantha Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame +89 more

Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk

BMC Medical Genomics(2024)10.1186/s12920-024-02024-0
N/A
0DataRank · unranked
10 citations

Jonathan R. Belyeu, Xiao Chen, Luis F. Paulin, Ngoc Quynh Nguyen, Emma Newman +21 more

Single-cell somatic copy number variants in brain using different amplification methods and reference genomes

Communications Biology(2024)10.1038/s42003-024-06940-w
N/A
0DataRank · unranked
8 citations

Zeliha Gözde Turan, Diego Pérez‐Rodríguez, Ida Bomann, Sairam Behera, Caoimhe Morley +6 more

Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.02.573821
N/A
0DataRank · unranked
39 citations

Severine Catreux, Massimiliano Rossi, Sean Truong, Zhuoyi Huang, Michael Ruehle +11 more

Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk

UNC Libraries(2024)10.17615/0jmh-f540
N/A
0DataRank · unranked
0 citations

Michael A. Eberle, Xiao Chen, Richard A. Gibbs, Emma Newman, Massimiliano Rossi +21 more

GREGoR: accelerating genomics for rare diseases

Nature(2025)10.1038/s41586-025-09613-8
N/A
0DataRank · unranked
15 citations

Ben Heavner, Marsha M. Wheeler, Rachel A. Ungar, Jonathan LoTempio, Laurens Wiel +94 more

A pan-genome approach to decipher variants in the highly complex tandem repeat of LPA

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.06.08.495395
N/A
0DataRank · unranked
11 citations

Sairam Behera, Ginger Metcalf, Richard A. Gibbs, Eric Boerwinkle, Fritz J. Sedlazeck +1 more

An international virtual hackathon to build tools for the analysis of structural variants within species ranging from coronaviruses to vertebrates

F1000Research(2021)10.12688/f1000research.51477.2
N/A
0DataRank · unranked
2 citations

Medhat Mahmoud, Michael D. Jochum, Daniel Paiva Agustinho, Barry Zorman, Ahmad Al Khleifat +57 more