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

Victoria Popic

Broad Institute

ORCID: 0000-0003-3181-5432

Also affiliated with Broadcom (Israel)

Biochemistry, Genetics and Molecular BiologyComputer 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 7%percentile
0.104Author 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.

A Murine Database of Structural Variants Enables the Genetic Architecture of a Spontaneous Murine Lymphoma to be Characterized

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.09.632219
Top 78%
0.104DataRank
Top 78%1 citations

Zhuoqing Fang, Egor Dolzhenko, Christopher T. Saunders, Zhuanfen Cheng, Victoria Popic +2 more

Papers

Driven by 9 papers — median percentile 22. Top paper: “High-throughput RNA isoform sequencing using programmed cDNA concatenation”.

High-throughput RNA isoform sequencing using programmed cDNA concatenation

Nature Biotechnology(2023)10.1038/s41587-023-01815-7
N/A
3.9DataRank · unranked
181 citations

Jonathan T. Smith, Kiran Garimella, Mehrtash Babadi, Victoria Popic, Moshe Sade-Feldman +14 more

Short read alignment with populations of genomes

Bioinformatics(2013)10.1093/bioinformatics/btt215
N/A
0.723DataRank · unranked
123 citations

Victoria Popic, Serafim Batzoglou, Lin Huang

Secure Discovery of Genetic Relatives Across Large-Scale and Distributed Genomic Datasets

Lecture notes in computer science(2024)10.1007/978-1-0716-3989-4_19
N/A
0.113DataRank · unranked
1 citations

David Froelicher, Ricky Magner, Victoria Popic, Bonnie Berger, Hyunghoon Cho +1 more

insilicoSV: a flexible grammar-based framework for structural variant simulation and placement

Bioinformatics(2025)10.1093/bioinformatics/btaf594
N/A
0.104DataRank · unranked
1 citations

Ning Jiang, Chris Rohlicek, Ilya Shlyakhter, Victoria Popic, Enzo Battistella

A Murine Database of Structural Variants Enables the Genetic Architecture of a Spontaneous Murine Lymphoma to be Characterized

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.09.632219
Top 78%
0.104DataRank
Top 78%1 citations

Zhuoqing Fang, Egor Dolzhenko, Christopher T. Saunders, Zhuanfen Cheng, Victoria Popic +2 more

Secure discovery of genetic relatives across large-scale and distributed genomic data sets

Genome Research(2024)10.1101/gr.279057.124
N/A
0DataRank · unranked
5 citations

David Froelicher, Ricky Magner, Victoria Popic, Bonnie Berger, Hyunghoon Cho +1 more

High-throughput RNA isoform sequencing using programmable cDNA concatenation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.01.462818
N/A
0DataRank · unranked
26 citations

Jonathan T. Smith, Kiran Garimella, Mehrtash Babadi, Moshe Sade-Feldman, Michael Gatzen +14 more

Graph-based deep reinforcement learning for haplotype assembly with Ralphi

Genome Research(2025)10.1101/gr.280569.125
N/A
0DataRank · unranked
1 citations

Anant Maheshwari, Barış Ekim, Bonnie Berger, Victoria Popic, Enzo Battistella

Cue: a deep-learning framework for structural variant discovery and genotyping

Nature Methods(2023)10.1038/s41592-023-01799-x
N/A
0DataRank · unranked
61 citations

Chris Rohlicek, Fabio Cunial, Iman Hajirasouliha, Dmitry Meleshko, Kiran Garimella +2 more