Mikhail Kolmogorov

Also affiliated with Foundation for the National Institutes of Health, National Cancer Institute, Center for Cancer Research

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological SciencesEnvironmental Science

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

18.0Author DataRank

Indexed papers

5in 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 5 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

The complete sequence of a human genome

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.26.445798

Top 2%

8.2DataRank

Top 2%182 citations

Sergey Koren, Arang Rhie, Allison A. Regier, Andrey V. Bzikadze, Alla Mikheenko +97 more

Papers

Driven by 25 papers — median percentile 87. Top paper: “metaFlye: scalable long-read metagenome assembly using repeat graphs”.

metaFlye: scalable long-read metagenome assembly using repeat graphs

Nature Methods(2020)10.1038/s41592-020-00971-x

N/A

9.6DataRank · unranked

1145 citations

Derek M. Bickhart, Bahar Behsaz, Alexey Gurevich, Mikhail Rayko, Sung Bong Shin +6 more

The complete sequence of a human genome

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.26.445798

Top 2%

8.2DataRank

Top 2%182 citations

Sergey Koren, Arang Rhie, Allison A. Regier, Andrey V. Bzikadze, Alla Mikheenko +97 more

The complete sequence of a human genome

Science(2022)10.1126/science.abj6987

Top 3%

7.0DataRank

Top 3%3361 citations

Sergey Koren, Arang Rhie, Allison A. Regier, Andrey V. Bzikadze, Alla Mikheenko +94 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

Automated assembly of high-quality diploid human reference genomes

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.06.483034

Top 28%

0.719DataRank

Top 28%22 citations

Giulio Formenti, Arang Rhie, Andrea Guarracino, Chentao Yang, Jonathan M. D. Wood +77 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

Personalized Pangenome References

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.12.13.571553

N/A

0DataRank · unranked

4 citations

Parsa Eskandar, Matteo Tommaso Ungaro, Hickey, Glenn, Jordan M. Eizenga, Adam M. Novak +7 more

Insights into the Mechanisms and Structure of Breakage-Fusion-Bridge Cycles in Cervical Cancer using Long-Read Sequencing

medRxiv(2023)10.1101/2023.08.21.23294276

N/A

0DataRank · unranked

2 citations

Nicole M. Rossi, Ayse Keskus, Yi Xie, Tanveer Ahmad, Asher Bryant +22 more

Personalized pangenome references

Nature Methods(2024)10.1038/s41592-024-02407-2

N/A

0DataRank · unranked

30 citations

Parsa Eskandar, Matteo Tommaso Ungaro, Hickey, Glenn, Jordan M. Eizenga, Adam M. Novak +7 more

Strainy: phasing and assembly of strain haplotypes from long-read metagenome sequencing

Nature Methods(2024)10.1038/s41592-024-02424-1

N/A

0DataRank · unranked

29 citations

Ataberk Donmez, M. S. Frolova, Mihai Pop, Mikhail Kolmogorov, Ekaterina Kazantseva

Insights into the mechanisms and structure of breakage-fusion-bridge cycles in cervical cancer using long-read sequencing

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.01.002

N/A

0DataRank · unranked

12 citations

Nicole M. Rossi, Ayse G. Keskus, Yi Xie, Tanveer Ahmad, Asher Bryant +22 more

The Utility of Long‐Read Sequencing in Diagnosing Early Onset Parkinson's Disease

Annals of Neurology(2024)10.1002/ana.27155

N/A

0DataRank · unranked

12 citations

Hiroyo Yoshino, Laksh Malik, Breeana Baker, Mayu Ishiguro, Rylee M. Genner +12 more

Severus: accurate detection and characterization of somatic structural variation in tumor genomes using long reads

medRxiv(2024)10.1101/2024.03.22.24304756

N/A

0DataRank · unranked

21 citations

Asher Bryant, Tanveer Ahmad, Byunggil Yoo, Sergey Aganezov, Anton Goretsky +33 more

DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologies

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.08.16.608331

N/A

0DataRank · unranked

19 citations

Daniel E. Cook, Pi-Chuan Chang, Alexey Kolesnikov, Lucas Brambrink, Juan Carlos Mier +26 more

Genetic regulation of TERT splicing contributes to reduced or elevated cancer risk by altering cellular longevity and replicative potential

medRxiv(2024)10.1101/2024.11.04.24316722

N/A

0DataRank · unranked

0 citations

Michelle Ho, Maxwell Hogshead, Chia‐Han Lee, Brenen W. Papenberg, Kaitlin Forsythe +18 more

Advancing long-read nanopore genome assembly and accurate variant calling for rare disease detection

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.002

N/A

0DataRank · unranked

42 citations

Sarah L. Stenton, Seth Berger, Paolo Canigiula, Brandy McNulty, Ivo Violich +18 more

Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencing

Nature Biotechnology(2025)10.1038/s41587-025-02618-8

N/A

0DataRank · unranked

28 citations

Asher Bryant, Tanveer Ahmad, Byunggil Yoo, Sergey Aganezov, Anton Goretsky +36 more

Genetic regulation of TERT splicing affects cancer risk by altering cellular longevity and replicative potential

Nature Communications(2025)10.1038/s41467-025-56947-y

N/A

0DataRank · unranked

15 citations

Michelle Ho, Maxwell H. Hogshead, Brenen W. Papenberg, Chia‐Han Lee, Kaitlin Forsythe +18 more

Unraveling the hidden complexity of cancer through long-read sequencing

Genome Research(2025)10.1101/gr.280041.124

N/A

0DataRank · unranked

10 citations

Ayse G. Keskus, Justin Wagner, Michal Izydorczyk, Winston Timp, Fritz J. Sedlazeck +5 more

Wakhan: reconstruction of chromosome-scale copy number profiles of tumor genomes with long-read sequencing

medRxiv(2025)10.64898/2025.12.11.25342098

N/A

0DataRank · unranked

0 citations

Ayse G. Keskus, Sergey Aganezov, Anton Goretsky, Isabel Rodriguez, Byunggil Yoo +23 more

Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads

Nature Methods(2021)10.1038/s41592-021-01299-w

N/A

0DataRank · unranked

332 citations

Trevor Pesout, Pi-Chuan Chang, Maria Nattestad, Alexey Kolesnikov, Sidharth Goel +9 more

Generating lineage-resolved, complete metagenome-assembled genomes from complex microbial communities

Nature Biotechnology(2022)10.1038/s41587-021-01130-z

N/A

0DataRank · unranked

237 citations

Mikhail Kolmogorov, Elizabeth Tseng, Daniel M. Portik, Anton Korobeynikov, Ivan Tolstoganov +12 more

Analyzing rare mutations in metagenomes assembled using long and accurate reads

Genome Research(2022)10.1101/gr.276917.122

N/A

0DataRank · unranked

7 citations

Mikhail Kolmogorov, Pavel A. Pevzner, Marcus W. Fedarko

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

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

Mikhail Kolmogorov

Indexed papers

Top data-sharing exemplar

Papers