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🔬 Laboratory Science

Molecular diagnostics, genomic surveillance, and experimental platforms powering our infectious disease research in Burundi and the Great Lakes Region.

Our Laboratory Capacity

Our laboratory program bridges clinical observation with molecular epidemiology. Working with the National Institute of Public Health (INSP) and international partners, we apply cutting-edge diagnostic and genomic tools to characterise pathogen diversity, resistance, and transmission dynamics across Burundi.

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Core Diagnostic Techniques

From rapid tests in the field to high-resolution genomic analysis

Serology

ELISA

Enzyme-Linked Immunosorbent Assay for quantitative detection of antibodies and antigens. Used for prevalence estimation and immunological profiling in population-level studies.

Malaria HIV SARS-CoV-2 Mpox
Molecular

PCR & qPCR

Conventional and quantitative polymerase chain reaction for sensitive detection of pathogen DNA/RNA, enabling diagnosis of subclinical and asymptomatic infections.

Plasmodium falciparum Tuberculosis Cholera HIV
Rapid Diagnosis

RDT (Rapid Diagnostic Tests)

Highly sensitive and conventional RDTs for field-deployable diagnosis. We evaluate hrp2/3 deletion status causing false-negative results — critical for malaria control in Burundi.

Malaria (PfHRP2/3) SARS-CoV-2
Genomics

Whole Genome Sequencing

End-to-end genomic sequencing of pathogens to characterise strain diversity, detect antimicrobial resistance mutations, and track outbreak origins and spread.

SARS-CoV-2 Monkeypox HIV Plasmodium Cholera
Genomics

Phylogenetic Analysis

Reconstruction of evolutionary and transmission histories using molecular clock models. Enables inference of when and where outbreaks originated and how they spread.

HIV-1 SARS-CoV-2 Mpox
Resistance

Drug Resistance Genotyping

Molecular genotyping of resistance markers to antimalarials, antibiotics, and antivirals. Identifies resistance mutations early to inform treatment guidelines and control measures.

Plasmodium (AMR) TB (AMR) Cholera (AMR)
Bioinformatics

Genomic Data Analysis

Bioinformatics pipelines using Linux command-line tools and R for sequence alignment, variant calling, phylogenetic inference, and QGIS-based geographic mapping of genomic data.

All pathogens QGIS Mapping R / Python
Spatial

Epidemiological Mapping

Spatial analysis of disease burden using QGIS and geostatistical methods. Generates risk maps to guide targeted interventions and health resource allocation.

Malaria Zoonoses NCDs
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Sequencing Platforms

Multi-platform capability for flexibility in pathogen genomics

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Illumina

Short-read, high-accuracy whole genome sequencing for SNP detection and variant calling

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Oxford Nanopore

Long-read, real-time sequencing enabling rapid outbreak response and structural variant detection

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DNBSeq

High-throughput sequencing for population-scale genomic surveillance studies

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CycloneSeq

Complementary platform for flexible pathogen sequencing in resource-limited settings

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Pathogen Surveillance Portfolio

Active molecular and genomic surveillance of key infectious diseases

Pathogen Disease Key Methods Priority
Plasmodium falciparum Malaria qPCR, RDT, WGS, hrp2/3 genotyping, AMR markers High
SARS-CoV-2 COVID-19 PCR, ELISA, WGS, Phylogenetics High
Monkeypox virus Mpox PCR, WGS, AI-powered surveillance High
Mycobacterium tuberculosis Tuberculosis PCR, AMR genotyping, WGS Moderate
HIV-1 HIV/AIDS Phylodynamics, ELISA, RNA evolutionary models Moderate
Vibrio cholerae Cholera PCR, WGS, AMR surveillance Active
Zoonotic pathogens Zoonoses Molecular typing, risk mapping, QGIS Ongoing
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Sample-to-Insight Workflow

From field collection to publication-ready findings

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Field Collection

Clinical & community sampling

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Lab Processing

Extraction & QC

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Diagnostics

PCR, ELISA, RDT

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Sequencing

Multi-platform WGS

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Bioinformatics

Analysis & phylogenetics

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Insights

Maps, models, policy

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Laboratory Research Focus Areas

Key scientific questions our laboratory program addresses

  • Asymptomatic malaria reservoir and transmission potential
  • hrp2/hrp3 deletions causing false-negative RDTs
  • Antimicrobial resistance genotyping in P. falciparum
  • Pathogen evolutionary dynamics via phylogenetics
  • Genomic surveillance of Mpox and SARS-CoV-2
  • Performance evaluation of diagnostic tests
  • HIV-1 genetic diversity in East Africa
  • Zoonotic spillover risk characterisation
  • RDT validation under field conditions
  • AMR surveillance: cholera and TB