Author

Paul M. K. Gordon

University of CalgaryORCID 0000-0003-2881-1713Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 3 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Research Focus:variant effect prediction· 3 Assay:whole-genome sequencing· 3 Research Focus:benchmarking· 2 Research Focus:database / resource· 2 Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2

Frequent Co-Authors

Anoosha SehariD· 2 shared Gary Van DomselaariD· 2 shared Ivan S. Gill· 2 shared Khushi Vora· 2 shared Madeline IsemingeriD· 2 shared Muhammad Zohaib AnwariD· 2 shared Quan LongiD· 2 shared William HsiaoiD· 2 shared

Activity by Year

2022-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersBioinformatics

Anoosha SeharORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

BioinformaticsNAR Genomics and BioinformaticsPeer-reviewedOct 7, 2025

VIRUS-MVP: A framework for comprehensive surveillance of viral mutations and their functional impacts

Muhammad Zohaib Anwar, Ivan S. Gill, Madeline Iseminger…·William Hsiao

VIRUS-MVP tracks viral mutations and their functional impacts across multiple viruses, providing tools for analysis and visualization.

2 citations

whole-genome sequencingstatistical model

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BioinformaticsNature CommunicationsPeer-reviewedJul 1, 2025

Apollo: A comprehensive GPU-powered within-host simulator for viral evolution and infection dynamics across population, tissue, and cell

Deshan Perera, Evan Li, Paul M. K. Gordon…·Quan Long

Apollo simulates within-host viral evolution and infection dynamics, validating limitations of transmission inference tools using HIV cohort data.

3 citations

humanwhole-genome sequencing

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GeneticsGeneticsPeer-reviewedFeb 5, 2024

An expression-directed linear mixed model (edLMM) discovering low-effect genetic variants

Qing Li, Jiayi Bian, Yanzhao Qian…·Quan Long

This paper introduces edLMM, a method that detects low-effect genetic variants using moderate sample sizes, improving missing heritability estimation.

1 citation

humanGWAS summary statistics

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BioinformaticsbioRxivPreprintJun 7, 2022

COVID-MVP: an interactive visualization for tracking SARS-CoV-2 mutations, variants, and prevalence, enabled by curated functional annotations and portable genomics workflow

Muhammad Zohaib Anwar, Ivan S. Gill, Madeline Iseminger…·William Hsiao

3 citations

viruswhole-genome sequencing

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