VIRAL SURVEILLANCE & COMPUTATIONAL GENOMICS
9 Packages • 13 Web Resources
Research Vision • Computational Biology • $2.27M Active Grants

Research Programs & Four Scientific Pillars

My computational biology program investigates how viral genomic variation and host regulatory networks shape infection outcomes, cross-species spillover, and disease severity. By uniting high-throughput diagnostic sequencing with context-aware machine learning and scalable web engineering, our work bridges molecular mechanism with real-time epidemiological impact.

Scientific Domains:#ViralSurveillance#Host-PathogenInteractomes#DeepLearning&AI#ProteinLanguageModels#NextflowDSL2#Metagenomics#Multi-OmicsIntegration#CropBioinformatics#StructuralModeling
Core Scientific Architecture

The Four Pillars of My Research Program

Each pillar represents a fundamental thrust of my computational biology research program, operating synergistically while contributing algorithms, datasets, and predictive models to an integrated discovery engine.

PILLAR 01pySeqRNA • SegVira • MetaNextViro

Viral Surveillance & Multi-Omics Discovery

Tracking viral evolution, quasispecies, and intra-host variation at the animal–human interface

Modern disease surveillance requires looking beyond consensus sequences to resolve the dynamic intra-host population structures of rapidly emerging pathogens. This pillar investigates the relationship between viral sequence variation and host transcriptional responses during infection and cross-species transmission events.

Key Research Directions & Methodologies:

Targeted amplicon sequencing and whole-genome reconstruction of emerging avian influenza (clade 2.3.4.4b H5N1), avian metapneumovirus (AMPV-A and AMPV-B), and porcine reproductive and respiratory syndrome virus (PRRSV-2).
Rigorous quantification of low-frequency intra-host single nucleotide variants (iSNVs ≥ 5%) and quasispecies diversity to capture adaptation before consensus fixation.
Pairing high-throughput viral genomics with host RNA-Seq transcriptomics to model viral replication kinetics, local tissue load, and differential cellularity across infection timecourses.
Deploying open Python and Cython analytical modules for automated variant calling, phylodynamic reconstruction, and diagnostic marker tracking.
PILLAR 02deepNEC 2.0 • deepHPI • SKEMPI 2.0 / PDBbind

Machine Learning & Context-Aware AI for Host–Pathogen Interactions

Bridging sequence representations with structural biophysics to forecast spillover potential

Sequence similarity alone often fails to explain why certain viral variants readily cross species barriers while closely related lineages remain restricted. This pillar develops multimodal machine learning architectures that combine sequence embeddings, structural interfaces, and host-receptor orthology to predict continuous interaction properties.

Key Research Directions & Methodologies:

Predicting continuous biophysical binding affinities (ΔΔG and dissociation constants Kd) rather than static binary interaction labels, trained on curated structural interaction datasets.
Quantitative sequence-to-affinity modeling of viral receptor-binding domains (e.g., influenza hemagglutinin) against α-2,3 and α-2,6 sialic acid glycan linkages from microarray profiles.
Developing alignment-free protein language model architectures for functional annotation and enzymatic classification, as demonstrated in deepNEC with >95% accuracy.
Enforcing strict homology-based test partitioning to prevent data leakage and ensure calibrated uncertainty estimation across out-of-distribution viral variants.
PILLAR 03HuCoPIA • HuPoxNET • Host Interactome Atlases

Comparative Systems Biology & Host Immune Networks

Mapping host cellular perturbations and innate immune evasion across species

When a pathogen encounters a new host, differences in outcome are governed by how effectively viral proteins disrupt or co-opt the host's intracellular regulatory networks. This pillar uses comparative network biology to discover conserved immune vulnerabilities and explain species-specific virulence differences.

Key Research Directions & Methodologies:

Comparative interactome modeling across reservoir species (wild aquatic birds, bats) and novel hosts (mammals, poultry, humans) to identify evolutionary divergence in host co-factors.
Evaluating how viral polymerase adaptations alter physical interactions with host nuclear replication machinery (such as host ANP32A/B co-factors) across species.
Analyzing how non-structural viral proteins (such as NS1 and PB1-F2) modulate pattern recognition receptors (RIG-I and MDA5) and dysregulate interferon-stimulated gene (ISG) cascades.
Prioritizing prospective therapeutic targets by integrating network centrality perturbation with functional viability constraints from high-throughput CRISPR knockout screens.
PILLAR 04Nextflow DSL2 • Docker / Singularity • Software & 13 Web Resources

Reproducible Software Architecture & Public Web Infrastructure

Translating algorithmic research into production-grade pipelines and accessible global platforms

Scientific discovery is accelerated when complex computational workflows are accessible, reproducible, and easy to run across heterogeneous computing environments. This pillar focuses on architecting enterprise-grade pipelines and publicly deployed web portals that serve the international research community.

Key Research Directions & Methodologies:

Engineering modular, containerized Nextflow DSL2 pipelines (MetaNextViro) with native support for Slurm HPC clusters, Docker, and Singularity runtime environments.
Deploying and maintaining interactive public web servers and databases accessed by researchers worldwide (kaabil.net and bioinfo.usu.edu).
Developing well-documented, open-source Python packages distributed via PyPI, GitHub, and Zenodo with checksum-verified model weights and versioned regression testing.
Building evidence-linked portals that present raw sequences, variant calls, and machine learning predictions with auditable provenance and confidence intervals.
Active Funding Portfolio • $2,269,435 in Awarded Grants

Awarded & Active Research Grants

Federal and foundation awards supporting pathogen genomic surveillance, host-pathogen interactomics, and rapid outbreak diagnostic intervention across agricultural and biological systems.

AWARDED • 2025 – Present • USDA-APHIS

Decoding the Poultry-HPAI Interactome: An Integrative Pipeline for Targeted Therapeutics Against Highly Pathogenic Avian Influenza

Investigator Role: Co-PI

$1,969,435
$799,443 SDSU Subaward

Decoding the poultry-HPAI interactome to develop an integrative pipeline for targeted therapeutics against Highly Pathogenic Avian Influenza. Incorporates multi-omics sequencing, structural interactomics, and viral surveillance.

USDA-APHISCo-PIHPAI H5N1Host-Pathogen InteractomeStructural Interactomics
ACTIVE • 2024 – Present • Foundation for Food & Agriculture Research (FFAR)

Emerging avian metapneumovirus subgroup A and B in US poultry: development of diagnostic assays and control strategies

Investigator Role: Co-PI

$150,000

Development of high-sensitivity diagnostic assays and control strategies for emerging avian metapneumovirus (aMPV) subgroups A and B causing outbreaks in US poultry flocks.

FFARCo-PIAvian MetapneumovirusDiagnostic AssaysControl Strategies
ACTIVE • 2024 – Present • Foundation for Food & Agriculture Research (FFAR) ROAR

Broad-spectrum live recombinant vaccine and improved diagnostics for emerging avian metapneumovirus subgroups A and B causing severe outbreaks in US poultry

Investigator Role: Co-I

$150,000

Rapid outbreak response for evaluating broad-spectrum live recombinant vaccines and improved diagnostics for emerging aMPV subgroups A and B.

FFAR ROARCo-IRecombinant VaccineDiagnosticsRapid Outbreak Response
Proposals in Pipeline • $2,100,500 Under Review

Submitted Proposals & Grants Under Review

Competitive research proposals submitted as Principal Investigator (PI) and Co-Investigator to USDA-AFRI and NIH R21 programs.

USDA-AFRI • PI$300,000

AI-Driven Genomic Surveillance and Control Strategies for Emerging Turkey Reoviruses (TRV)

AI-driven computational genomic surveillance, molecular evolution modeling, and intervention strategies for emerging turkey reoviruses.

USDA-AFRIPIAI SurveillanceTurkey ReovirusMolecular Evolution
USDA-AFRI • PI$300,000

BRIDGE: A host-pathogen interactome and machine learning platform to predict zoonotic risk of livestock and poultry viruses

Developing a host-pathogen interactome and deep learning platform to forecast cross-species transmission and zoonotic spillover risk.

USDA-AFRIPIMachine LearningHost-Pathogen InteractomeZoonotic Risk
DHHS / National Institutes of Health (NIH) • Co-I$400,500

Innovative approaches for early detection and control of zoonotic influenza viruses in poultry

Innovative computational and experimental approaches for early detection, variant characterization, and control of zoonotic influenza viruses.

NIH R21Co-IZoonotic InfluenzaEarly DetectionSurveillance
USDA-AFRI • Co-PI$300,000

Novel mass administration vaccine for humoral and cellular immunity using mRNA plus virus like particle

Computational design and evaluation of mass-administration mRNA and virus-like particle (VLP) vaccine platforms for agricultural livestock.

USDA-AFRICo-PImRNA VaccineVLPComputational Design
USDA-AFRI • Co-PI$800,000

Systems-Level Host Interactome Framework for Avian Metapneumovirus Mitigation: Advancing Therapeutics to Strengthen US Agricultural Biosecurity

Systems-level host interactome framework modeling host-pathogen protein networks to advance antiviral discovery and biosecurity defenses.

USDA-AFRICo-PISystems BiologyInteractomeAgricultural Biosecurity
Collaborative Horizons • Computational Biology Direction

Bridging High-Performance Computing with Diagnostic Reality

Computational biology is at its best when algorithms are continually calibrated against real diagnostic samples and biological reality. By anchoring our computational pipelines directly in high-throughput sequencing workflows and active pathogen outbreak surveillance, our tools are tested against real-world biological complexity rather than idealized theoretical datasets.

Whether uncovering novel zoonotic spillover markers, building containerized Nextflow pipelines for high-performance clusters, or deploying accessible web servers for global scientists, my program is committed to open, reproducible, and interdisciplinary computational science.