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John V. Heymach

dblp:129/6044 · DBLP profile ↗
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2ranked-venue papers
0as first author
1since 2021 · last 2023
0000-0001-9068-8942ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 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
1 paper
Bioinformatics and computational biology · 50% Medical and health informatics · 50%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Medical and health informatics
dose-response modeling
0.212015
drexplorer: A tool to explore dose-response relationships and drug-drug interactions · Bioinform. 2015
Bioinformatics and computational biology › clinical bioinformatics
drug response analysis
0.212015
drexplorer: A tool to explore dose-response relationships and drug-drug interactions · Bioinform. 2015

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

nonlinear dose-response modeling · 0.2IC50 estimation · 0.2
YearPublicationVenuePosition
2023 A novel statistical method for decontaminating T-cell receptor sequencing data
abstract
The T-cell receptor (TCR) repertoire is highly diverse among the population and plays an essential role in initiating multiple immune processes. TCR sequencing (TCR-seq) has been developed to profile the T cell repertoire. Similar to other high-throughput experiments, contamination can happen during several steps of TCR-seq, including sample collection, preparation and sequencing. Such contamination creates artifacts in the data, leading to inaccurate or even biased results. Most existing methods assume 'clean' TCR-seq data as the starting point with no ability to handle data contamination. Here, we develop a novel statistical model to systematically detect and remove contamination in TCR-seq data. We summarize the observed contamination into two sources, pairwise and cross-cohort. For both sources, we provide visualizations and summary statistics to help users assess the severity of the contamination. Incorporating prior information from 14 existing TCR-seq datasets with minimum contamination, we develop a straightforward Bayesian model to statistically identify contaminated samples. We further provide strategies for removing the impacted sequences to allow for downstream analysis, thus avoiding any need to repeat experiments. Our proposed model shows robustness in contamination detection compared with a few off-the-shelf detection methods in simulation studies. We illustrate the use of our proposed method on two TCR-seq datasets generated locally.
Ruoxing Li, Mehmet Altan, Alexandre Reuben, Ruitao Lin, John V. Heymach, Runzhe Chen, Latasha Little, Shawna Hubert, Ziyi Li 0001
Briefings Bioinform.5
2015 drexplorer: A tool to explore dose-response relationships and drug-drug interactions
abstract
Abstract Motivation: Nonlinear dose–response models are primary tools for estimating the potency [e.g. half-maximum inhibitory concentration (IC) known as IC50] of anti-cancer drugs. We present drexplorer software, which enables biologists to evaluate replicate reproducibility, detect outlier data points, fit different models, select the best model, estimate IC values at different percentiles and assess drug–drug interactions. drexplorer serves as a computation engine within the R environment and a graphical interface for users who do not have programming backgrounds. Availability and implementation: The drexplorer R package is freely available from GitHub at https://github.com/nickytong/drexplorer. A graphical user interface is shipped with the package. Contact: [email protected] Supplementary information: Supplementary data are available at Bioinformatics online.
Pan Tong, Kevin R. Coombes, Faye M. Johnson, Lauren A. Byers, Lixia Diao, Diane D. Liu, J. Jack Lee, John V. Heymach, Jing Wang 0006
Bioinform.8