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Welles Robinson

dblp:238/9827 · DBLP profile ↗
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4ranked-venue papers
1as first author
2since 2021 · last 2025
0000-0001-9018-6811ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 4 · 1 first-author · 2 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
4 papers
Bioinformatics and computational biology · 93% Computational science and engineering · 7%

Topics — the 8 heaviest of 8, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
cancer genomics
1.842025
Determining Optimal Placement of Copy Number Aberration Impacted Single Nucleotide Variants in a Tumor Progression History · RECOMB 2024
Modeling clinical and molecular covariates of mutational process activity in cancer · Bioinform. 2019
A Sticky Multinomial Mixture Model of Strand-Coordinated Mutational Processes in Cancer · RECOMB 2019
Bioinformatics and computational biology › genomics
computational genomics
0.912025
A Partition Function Algorithm to Evaluate Inferred Subclonal Structures in Single-Cell Sequencing Data · RECOMB 2025
Bioinformatics and computational biology › single-cell analysis
single-cell sequencing
0.912025
A Partition Function Algorithm to Evaluate Inferred Subclonal Structures in Single-Cell Sequencing Data · RECOMB 2025
Bioinformatics and computational biology › cancer genomics
tumor progression
0.812024
Determining Optimal Placement of Copy Number Aberration Impacted Single Nucleotide Variants in a Tumor Progression History · RECOMB 2024
Computational science and engineering › latent variable model
mixture model
0.412019
A Sticky Multinomial Mixture Model of Strand-Coordinated Mutational Processes in Cancer · RECOMB 2019
Bioinformatics and computational biology › cancer genomics
mutational signature analysis
0.412019
Modeling clinical and molecular covariates of mutational process activity in cancer · Bioinform. 2019
Bioinformatics and computational biology › biostatistics › statistical bioinformatics
statistical genomics
0.412019
A Sticky Multinomial Mixture Model of Strand-Coordinated Mutational Processes in Cancer · RECOMB 2019
Bioinformatics and computational biology › cancer genomics › tumor evolution
clonal evolution
0.312025
A Partition Function Algorithm to Evaluate Inferred Subclonal Structures in Single-Cell Sequencing Data · RECOMB 2025

Methods — techniques the papers use, named apart from their topics

partition function algorithm · 0.9combinatorial optimization · 0.8non-negative matrix factorization · 0.4multinomial mixture model · 0.4markov model · 0.4bayesian topic modeling · 0.4
YearPublicationVenuePosition
2025 A Partition Function Algorithm to Evaluate Inferred Subclonal Structures in Single-Cell Sequencing Data
Farid Rashidi Mehrabadi, Erfan Sadeqi Azer, John D. Bridgers, Eva Pérez-Guijarro, Kerrie Marie, Howard H. Yang, Charli Gruen, Chih Hao Wu, Welles Robinson, Huaitian Liu, Can Kizilkale, Michael C. Kelly, Cari Smith, Sung Chin, Jessica Ebersole, Sandra Burkett, Aydin Buluç, Maxwell P. Lee, Erin K. Molloy, Teresa M. Przytycka, Glenn Merlino, Chi-Ping Day, Salem Malikic, Funda Ergün, Süleyman Cenk Sahinalp
RECOMB9
2024 Determining Optimal Placement of Copy Number Aberration Impacted Single Nucleotide Variants in a Tumor Progression History
Chih Hao Wu, Suraj Joshi, Welles Robinson, Paul F. Robbins, Russell Schwartz, Süleyman Cenk Sahinalp, Salem Malikic
RECOMB3
2019 A Sticky Multinomial Mixture Model of Strand-Coordinated Mutational Processes in Cancer
Itay Sason, Damian Wójtowicz, Welles Robinson, Mark D. M. Leiserson, Teresa M. Przytycka, Roded Sharan
RECOMB3
2019 Modeling clinical and molecular covariates of mutational process activity in cancer
abstract
MOTIVATION: Somatic mutations result from processes related to DNA replication or environmental/lifestyle exposures. Knowing the activity of mutational processes in a tumor can inform personalized therapies, early detection, and understanding of tumorigenesis. Computational methods have revealed 30 validated signatures of mutational processes active in human cancers, where each signature is a pattern of single base substitutions. However, half of these signatures have no known etiology, and some similar signatures have distinct etiologies, making patterns of mutation signature activity hard to interpret. Existing mutation signature detection methods do not consider tumor-level clinical/demographic (e.g. smoking history) or molecular features (e.g. inactivations to DNA damage repair genes). RESULTS: To begin to address these challenges, we present the Tumor Covariate Signature Model (TCSM), the first method to directly model the effect of observed tumor-level covariates on mutation signatures. To this end, our model uses methods from Bayesian topic modeling to change the prior distribution on signature exposure conditioned on a tumor's observed covariates. We also introduce methods for imputing covariates in held-out data and for evaluating the statistical significance of signature-covariate associations. On simulated and real data, we find that TCSM outperforms both non-negative matrix factorization and topic modeling-based approaches, particularly in recovering the ground truth exposure to similar signatures. We then use TCSM to discover five mutation signatures in breast cancer and predict homologous recombination repair deficiency in held-out tumors. We also discover four signatures in a combined melanoma and lung cancer cohort-using cancer type as a covariate-and provide statistical evidence to support earlier claims that three lung cancers from The Cancer Genome Atlas are misdiagnosed metastatic melanomas. AVAILABILITY AND IMPLEMENTATION: TCSM is implemented in Python 3 and available at https://github.com/lrgr/tcsm, along with a data workflow for reproducing the experiments in the paper. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Welles Robinson, Roded Sharan, Mark D. M. Leiserson
Bioinform.1