Genomics Core Facilities in Uganda
Engineering Excellence & Technical Support
Genomics Core Facilities solutions for Research & Discovery (R&D). High-standard technical execution following OEM protocols and local regulatory frameworks.
Next-Generation Sequencing (NGS) Powerhouse
Empowering Ugandan researchers with cutting-edge NGS platforms for rapid and cost-effective whole-genome sequencing, transcriptomics, and epigenomics. Accelerating discoveries in infectious diseases, agriculture, and human health.
Advanced Bioinformatics & Data Analysis
Providing robust bioinformatics support and cloud-based infrastructure for processing, analyzing, and interpreting large-scale genomic datasets. Transforming raw sequence data into actionable scientific insights.
Genomic Surveillance & Disease Monitoring
Contributing to national health security through high-throughput genomic surveillance of pathogens. Enabling timely detection, tracking, and response to outbreaks, safeguarding public health in Uganda.
What Is Genomics Core Facilities In Uganda?
Genomics Core Facilities in Uganda are specialized service units that provide access to advanced genomic technologies, expertise, and infrastructure for researchers and institutions. These facilities are crucial for enabling high-throughput DNA sequencing, genotyping, bioinformatics analysis, and other molecular biology applications that underpin modern biological and biomedical research. Their primary objective is to democratize access to cutting-edge genomic tools, reducing the financial and technical barriers for Ugandan scientists to conduct world-class research. This involves operating and maintaining sophisticated instrumentation, offering expert technical support, developing and implementing standardized protocols, and providing data analysis and interpretation services. The services are essential for researchers across various disciplines, including public health, infectious diseases, agriculture, environmental science, and human genetics, facilitating a deeper understanding of Uganda's unique biodiversity and health challenges.
| Who Needs Genomics Core Facilities? | Typical Use Cases | |||||
|---|---|---|---|---|---|---|
| Academic and Research Institutions: Universities, national research institutes, and affiliated laboratories seeking to conduct genomic studies without investing in expensive individual infrastructure. | Public Health Agencies: Ministries of Health and related organizations involved in disease surveillance, outbreak investigations, pathogen genomics, and antimicrobial resistance monitoring (e.g., tracking the evolution of HIV, malaria, or emerging infectious diseases like COVID-19). | Agricultural Research Organizations: Institutions focused on crop improvement, livestock breeding, pest and disease management, and understanding the genetic basis of agricultural traits relevant to Uganda's food security. | Environmental Scientists: Researchers studying biodiversity, ecological genomics, conservation efforts, and the impact of environmental changes on various species. | Clinical Research Groups: Medical researchers investigating genetic predispositions to diseases, pharmacogenomics, and personalized medicine approaches. | Biotechnology Companies: Early-stage companies or established entities requiring genomic services for product development or R&D in areas like diagnostics or therapeutics. | Students and Trainees: Individuals undertaking postgraduate research or professional development requiring hands-on experience with genomic technologies and data analysis. |
| Infectious Disease Epidemiology: Sequencing pathogens to track transmission routes, identify drug resistance mutations, and monitor viral/bacterial evolution (e.g., surveillance of HIV drug resistance, characterizing novel viral strains). | Human Genetics and Disease Research: Identifying genetic variants associated with local disease burdens (e.g., sickle cell disease, non-communicable diseases), population genetics studies, and ancestral profiling. | Agricultural Genomics: Genomic selection for improved crop yields and disease resistance, characterizing genetic diversity in local livestock breeds, and identifying genes for climate resilience. | Conservation Genomics: Assessing genetic diversity within endangered species, defining conservation units, and understanding population structure for effective wildlife management. | Metagenomics: Studying microbial communities in various environments (e.g., soil, water, human gut) to understand their function and ecological roles. | Transcriptomics (RNA-Seq): Investigating gene expression patterns under different conditions to understand biological pathways, cellular responses, and disease mechanisms. | Diagnostic Development: Providing genomic data to support the development and validation of novel diagnostic tests for infectious or genetic diseases. |
Key Services Offered by Genomics Core Facilities
- Next-Generation Sequencing (NGS) services (e.g., whole-genome sequencing, exome sequencing, RNA-Seq, amplicon sequencing).
- Genotyping services (e.g., SNP arrays, microsatellite analysis).
- DNA/RNA extraction and quality control.
- Bioinformatics analysis pipelines (e.g., variant calling, transcriptome assembly, phylogenetic analysis).
- Consultation and project design support.
- Training and capacity building in genomics techniques and data analysis.
Who Needs Genomics Core Facilities In Uganda?
Genomics core facilities are indispensable resources for advancing biological and biomedical research in Uganda. They provide access to state-of-the-art technologies and expertise that are crucial for understanding the genetic basis of diseases, improving agricultural yields, conserving biodiversity, and driving innovation in biotechnology. Without these facilities, many research projects would be severely hampered or impossible, limiting Uganda's capacity to address its unique health, agricultural, and environmental challenges through cutting-edge scientific approaches.
| Customer/Department | Key Needs/Applications | Examples of Research/Services |
|---|---|---|
| Academic & Research Institutions (Universities, Research Institutes) | Disease genomics, host-pathogen interactions, drug discovery, fundamental biology, training of future scientists. | Whole genome sequencing of infectious agents (malaria, HIV, TB), identifying genetic risk factors for non-communicable diseases, plant genomics for crop improvement, microbiome studies. |
| Healthcare & Public Health Sector (Hospitals, Public Health Labs, Ministry of Health) | Diagnostic genomics, outbreak investigations, personalized medicine (emerging), surveillance of infectious diseases, antibiotic resistance monitoring. | Rapid identification of pathogens during outbreaks, prenatal screening (future), understanding genetic predispositions to common diseases, tracking the evolution of viruses and bacteria. |
| Agricultural & Food Security Organizations (National Agricultural Research Organizations, CGIAR Centers, NGOs) | Crop and livestock improvement, pest and disease resistance, understanding genetic diversity, climate change adaptation, sustainable agriculture. | Genomic selection for drought-tolerant crops, identifying genes for disease resistance in livestock, characterizing germplasm for conservation, developing climate-resilient varieties. |
| Conservation & Environmental Agencies (National Environment Management Authority, Wildlife Authorities, Forestry Departments) | Biodiversity assessment, species identification, conservation genetics, understanding ecological interactions, wildlife forensics. | DNA barcoding of species for monitoring, population genetics studies for endangered species, tracking illegal wildlife trade, studying the impact of environmental changes on genetic diversity. |
| Biotechnology & Pharmaceutical Industries (Emerging) | Drug target identification, bioprospecting, development of diagnostics and therapeutics, quality control. | Screening natural products for bioactive compounds, developing novel diagnostic kits, research into gene therapy (long-term). |
| Government Ministries & Policymakers (e.g., Ministry of Science and Technology, Ministry of Agriculture, Ministry of Health) | Informed policy development, national strategic planning for health and agriculture, evidence-based decision-making, capacity building. | Providing scientific data to inform public health strategies, guiding agricultural research priorities, supporting the development of national biotechnology policies. |
Target Customers and Departments for Genomics Core Facilities in Uganda:
- Academic and Research Institutions
- Healthcare and Public Health Sectors
- Agricultural and Food Security Organizations
- Conservation and Environmental Agencies
- Biotechnology and Pharmaceutical Industries (Emerging)
- Government Ministries and Policymakers
Genomics Core Facilities Process In Uganda
Genomics core facilities in Uganda, like their international counterparts, operate through a structured workflow to ensure efficient and accurate genomic services. This process typically begins with an initial inquiry from a researcher or institution seeking specific genomic analyses. The facility then engages in a consultation phase to understand the project's scope, experimental design, and required services. Following this, a detailed proposal and quote are generated, outlining the costs, timelines, and deliverables. Upon agreement, the client prepares and submits biological samples, adhering to the facility's submission guidelines. The samples then undergo a series of quality control checks before proceeding to the chosen genomic assay (e.g., sequencing, genotyping). Data generation is followed by rigorous bioinformatics analysis and interpretation. Finally, a comprehensive report is delivered to the client, often accompanied by a debriefing session to discuss the results and their implications.
| Stage | Description | Key Activities | Responsible Parties | Typical Duration (Illustrative) |
|---|---|---|---|---|
| Inquiry & Initial Contact | The potential client expresses interest in the facility's services. | Contacting the facility via email, phone, or website form. Inquiring about specific services and capabilities. | Client, Genomics Core Facility Administration/Client Services | 1-3 business days |
| Consultation & Project Planning | Detailed discussion to understand project needs and feasibility. | Meetings (in-person/virtual) to discuss experimental goals, sample types, desired analyses, bioinformatics requirements, and timelines. Defining the scope of work. | Client (PI, researcher), Genomics Core Facility (Scientific Staff, Project Manager) | 2-7 business days |
| Proposal & Quotation | Formal documentation of agreed-upon services, costs, and timelines. | Generating a detailed project proposal outlining the methodology, expected results, timeline, and cost breakdown. Client review and approval. | Genomics Core Facility (Project Manager, Administration), Client | 3-7 business days |
| Sample Submission & Receipt | The client prepares and delivers biological samples to the facility. | Following submission guidelines (e.g., DNA extraction methods, storage, shipping). Completing submission forms. Facility acknowledges receipt of samples. | Client, Genomics Core Facility (Lab Technicians, Sample Management) | Varies by sample preparation (client-side) + 1-2 business days (receipt) |
| Sample Quality Control (QC) | Assessing the quality and quantity of submitted samples before assay execution. | Measuring DNA/RNA concentration and purity (e.g., Nanodrop, Qubit). Assessing integrity (e.g., gel electrophoresis, Bioanalyzer). | Genomics Core Facility (Lab Technicians) | 1-5 business days (per batch) |
| Genomic Assay Execution | Performing the selected molecular biology techniques. | Library preparation (for sequencing), PCR, genotyping assays, etc. Performing the primary genomic analysis based on project requirements. | Genomics Core Facility (Lab Technicians, Scientists) | Highly variable (days to weeks, depending on assay complexity) |
| Data Generation | Producing raw genomic data from the assays. | Sequencing run (e.g., Illumina), microarray scanning, etc. | Genomics Core Facility (Sequencing Specialists, Instrument Operators) | Highly variable (days to weeks, depending on instrument throughput) |
| Bioinformatics Analysis & Interpretation | Processing and analyzing the raw data to extract meaningful biological insights. | Raw data quality control, alignment, variant calling, gene expression analysis, statistical analysis, visualization. Interpretation of results in the context of the research question. | Genomics Core Facility (Bioinformaticians, Computational Biologists), Client (for biological interpretation) | Highly variable (weeks to months, depending on data size and complexity) |
| Data & Report Delivery | Providing the analyzed results and relevant documentation to the client. | Delivery of raw data, processed data, and a comprehensive final report. May include figures, tables, and interpretation summaries. Secure data transfer. | Genomics Core Facility (Bioinformaticians, Project Manager), Client | 1-5 business days |
| Post-Analysis Support & Debriefing | Assisting the client with understanding and utilizing the results. | Follow-up meetings to discuss the report, answer questions, and provide guidance on next steps. Potential collaboration on manuscript preparation or further research. | Genomics Core Facility (Scientific Staff, Project Manager), Client | Ongoing (as needed) |
Genomics Core Facility Workflow Stages
- Inquiry & Initial Contact
- Consultation & Project Planning
- Proposal & Quotation
- Sample Submission & Receipt
- Sample Quality Control
- Genomic Assay Execution
- Data Generation
- Bioinformatics Analysis & Interpretation
- Data & Report Delivery
- Post-Analysis Support & Debriefing
Genomics Core Facilities Cost In Uganda
Genomics core facilities in Uganda, while still developing, are crucial for advancing research and diagnostics. The cost of accessing these services is influenced by several factors, including the type of assay or service, the complexity of the workflow, the amount of sample processed, the technology platform utilized, and the expertise required from the facility staff. These facilities often aim to strike a balance between providing affordable access for local researchers and covering their operational costs, which include instrument maintenance, consumables, and personnel salaries. Pricing is typically presented in Ugandan Shillings (UGX).
| Service Category | Typical Pricing Range (UGX) | Notes |
|---|---|---|
| Basic DNA/RNA Extraction | 20,000 - 70,000 per sample | Depends on sample type (blood, tissue, etc.) and kit used. |
| Standard PCR / qPCR | 15,000 - 50,000 per reaction | Includes primers, master mix, and instrument time. Prices can vary based on multiplexing. |
| Sanger Sequencing (per read) | 30,000 - 80,000 per reaction | Covers sequencing reaction and basic data output. Higher for longer amplicons. |
| Whole Genome Sequencing (WGS) - Per Gb | 150,000 - 400,000+ per Gb | Highly variable based on platform, coverage, and bioinformatics. This is a broad estimate as full WGS projects are significant investments. |
| Whole Exome Sequencing (WES) - Per Sample | 1,500,000 - 4,000,000+ per sample | Includes library preparation, sequencing, and basic variant calling. Bioinformatics analysis adds significantly. |
| Targeted Sequencing (e.g., gene panels) | 500,000 - 2,500,000+ per sample | Depends on the size and complexity of the gene panel and required coverage. |
| Library Preparation (NGS) | 200,000 - 700,000 per sample | Cost varies significantly based on the chosen library preparation kit and the type of sequencing library. |
| Basic Bioinformatics Analysis (e.g., QC, alignment) | Negotiable/Project-based | Often an add-on service. Hourly rates or project fees apply. |
Key Pricing Factors for Genomics Core Facilities in Uganda
- Assay Type: Simple PCR-based assays are generally less expensive than complex next-generation sequencing (NGS) experiments.
- Sequencing Depth/Coverage: For NGS, the required depth of sequencing significantly impacts cost. Higher coverage for more detailed analysis demands more sequencing reagent and instrument time.
- Sample Throughput: Bulk processing of samples can sometimes lead to economies of scale, but the initial setup and library preparation costs remain.
- Technology Platform: Different sequencing technologies (e.g., Illumina, Oxford Nanopore) have varying reagent and instrument costs.
- Bioinformatics Analysis: The level of data analysis required, from basic variant calling to complex pathway analysis, adds to the overall cost.
- Consumables: Reagents, kits, and lab supplies are a major component of pricing.
- Instrument Time & Maintenance: Costs associated with running and maintaining sophisticated equipment are factored in.
- Personnel Expertise: Specialized technicians and bioinformaticians command higher salaries, which are reflected in service costs.
- Facility Overhead: Rent, utilities, and administrative expenses contribute to the pricing structure.
- Subsidies/Grants: Some facilities may offer subsidized rates for academic researchers or those supported by specific grants, leading to price variations.
Affordable Genomics Core Facilities Options
Accessing high-throughput genomic technologies can be a significant investment for research institutions and individual labs. Thankfully, several options exist to make genomics core facilities more affordable. These include exploring shared resource facilities, understanding value bundles, and implementing various cost-saving strategies. Core facilities, whether institutional, consortia-based, or even commercial service providers offering tiered pricing, are designed to democratize access to expensive equipment and specialized expertise. By pooling resources and sharing costs, researchers can benefit from cutting-edge technologies without the burden of individual ownership and maintenance.
| Strategy | Description | Potential Savings |
|---|---|---|
| Value Bundles | Packages of services offered at a discounted rate compared to purchasing each service individually. Examples include a 'whole-genome sequencing package' or a 'single-cell RNA-seq bundle' that might include library preparation, sequencing, and basic bioinformatics analysis. | 10-30% or more, depending on the bundle and provider. |
| Bulk Purchasing Discounts | Negotiating lower prices by committing to a large volume of services over a defined period. | Can be significant, especially for large research projects or ongoing needs. |
| Collaborative Grant Applications | Seeking funding from grants that specifically support shared resources or core facility development. This can offset operational costs. | Direct funding for core services, reducing the burden on individual labs. |
| Standardized Protocols & Reagents | Adopting standardized workflows and utilizing bulk-purchased reagents can reduce per-sample costs and improve efficiency. | 5-15% reduction in reagent and labor costs. |
| In-house vs. Outsourcing Analysis | Carefully evaluating whether complex bioinformatics analysis is more cost-effective when done in-house (requiring expertise and infrastructure) or outsourced to the core facility or a commercial provider. | Varies greatly, but can save tens of thousands of dollars annually by avoiding unnecessary infrastructure or personnel costs. |
| Early Project Planning & Consultation | Engaging with core facility staff early in project design to optimize experimental design, select appropriate technologies, and avoid costly mistakes or redundant experiments. | Can prevent wasted resources and rework, potentially saving thousands of dollars in failed experiments. |
| Training and Education | Investing in training for researchers to perform certain sample preparation steps in-house, if feasible and cost-effective, or to better understand core facility services and data interpretation. | Reduces reliance on core staff for routine tasks, freeing up their time and potentially lowering overall service fees. |
| Tiered Pricing Models | Choosing the most appropriate service level (e.g., basic vs. premium analysis, standard vs. rapid turnaround) based on project needs and budget constraints. | Allows for cost optimization by not overpaying for features not required. |
Key Affordable Genomics Core Facility Options and Strategies
- {"title":"Institutional Core Facilities","description":"University or hospital-based cores offering access to a wide range of genomic services (sequencing, genotyping, etc.) at subsidized rates for affiliated researchers. Often have dedicated staff and a variety of technology platforms."}
- {"title":"Consortium or Multi-Institutional Cores","description":"Collaborative efforts between multiple institutions to share resources, equipment, and expertise. This can lead to greater purchasing power and a broader range of available technologies."}
- {"title":"Commercial Genomics Service Providers","description":"Companies that offer genomics services on a fee-for-service basis. Many provide tiered pricing based on throughput, complexity, and turnaround time, making them accessible for various budget levels."}
- {"title":"Shared Resource Platforms","description":"Similar to institutional cores but can be more specialized. For example, a 'proteomics and genomics' shared platform might offer both services under one umbrella."}
- {"title":""Pay-as-you-go" Models","description":"Cores that charge per sample, per run, or per service, allowing researchers to control costs by only paying for what they use."}
Verified Providers In Uganda
In Uganda's burgeoning healthcare landscape, identifying truly verified and high-quality healthcare providers is paramount for ensuring patient safety and optimal outcomes. Franance Health stands out as a beacon of excellence, demonstrating a rigorous commitment to credentialing and patient-centered care. This document outlines the key credentials that define Franance Health and explains why they represent the best choice for individuals and families seeking reliable healthcare services in Uganda.
| Credential Aspect | Franance Health's Commitment | Why it Matters to Patients |
|---|---|---|
| MoH Accreditation | Fully compliant with all MoH regulations and quality standards. | Ensures services meet national safety and efficacy benchmarks. |
| Staff Qualifications | All doctors, nurses, and specialists are board-certified and licensed. | Guarantees that you are treated by competent and experienced professionals. |
| International Standards | Actively collaborates with international bodies for knowledge exchange and best practice adoption. | Access to world-class medical expertise and treatment methodologies. |
| Patient Feedback | Consistently achieves high patient satisfaction ratings through regular surveys. | Provides a reliable indicator of excellent care and positive patient experiences. |
| Technology Investment | Equipped with state-of-the-art diagnostic and treatment equipment. | Enables accurate diagnosis and effective treatment with minimal invasiveness. |
| Safety Protocols | Implements stringent infection control measures in all facilities. | Minimizes the risk of hospital-acquired infections and ensures a safe healing environment. |
| Staff Training | Regularly invests in ongoing training and development for all healthcare personnel. | Ensures that staff are proficient in the latest medical procedures and technologies. |
Key Credentials of Franance Health:
- Accreditation by the Uganda Ministry of Health (MoH) - Demonstrates adherence to national healthcare standards and regulations.
- Professional Licensing and Certification of Medical Staff - Ensures all healthcare professionals possess the necessary qualifications and are legally permitted to practice.
- Partnerships with Reputable International Health Organizations - Indicates a commitment to global best practices and continuous quality improvement.
- Independent Patient Feedback and Satisfaction Scores - Provides transparent evidence of patient experience and service quality.
- Investment in Advanced Medical Technology and Infrastructure - Showcases a dedication to providing cutting-edge diagnostic and treatment capabilities.
- Robust Infection Prevention and Control Protocols - Highlights a proactive approach to patient safety and disease prevention.
- Commitment to Continuous Professional Development for Staff - Guarantees that medical teams remain up-to-date with the latest medical advancements.
Scope Of Work For Genomics Core Facilities
This Scope of Work (SOW) outlines the technical deliverables and standard specifications for services provided by the Genomics Core Facility. The facility offers a comprehensive suite of genomic services designed to support research across various disciplines. The aim is to provide high-quality, reproducible, and reliable genomic data to facilitate scientific discovery.
| Service Category | Technical Deliverable | Standard Specification/Requirement | Example Metrics/Acceptance Criteria |
|---|---|---|---|
| NGS Library Preparation | Genomic DNA or RNA library | Library yield > 500 ng, insert size distribution appropriate for application (e.g., 300-500 bp for Illumina paired-end), adapter contamination < 5% | Bioanalyzer/TapeStation profile, Qubit quantification, Adapter dimer analysis (e.g., via gel electrophoresis or sequencing) |
| NGS Sequencing | Raw sequencing reads (FASTQ format) | Minimum data output per run as per instrument capacity (e.g., > 100 Gb for Illumina NovaSeq), read length and quality scores (Phred score > Q30 for > 80% of bases) | Sequencing report including cluster density, Q30 statistics, base distribution, GC content, and number of reads passing filter |
| CRISPR/Cas9 Screening | Guide RNA library sequencing and demultiplexed read counts | Coverage > 100x per guide RNA, minimal read errors, accurate guide RNA identification | Demultiplexed FASTQ files for each sample, guide RNA abundance table with confidence scores |
| Single-Cell RNA Sequencing | Count matrix (genes x cells), UMI counts, cell metadata | Minimum number of cells captured per sample (e.g., > 5,000), average UMI counts per cell > 1,000, percentage of reads mapping to mitochondrial genes < 15% | Filtered count matrix, QC report including number of genes per cell, UMI counts per cell, and mitochondrial gene percentage |
| Genotyping/SNP Analysis | VCF file with identified SNPs and genotypes | SNP call rate > 95%, genotype concordance > 98% for technical replicates | VCF file, genotype quality scores, sample QC metrics (e.g., heterozygosity rate, call rate) |
| Long-Read Sequencing | High-quality contiguous sequences (FASTA format) or base-called FASTQ | Read length N50 > 10 kb, low indel error rate (< 5%) | Base-called FASTQ files, assembly statistics (e.g., N50, contig count) |
| Metagenomics | Taxonomic profiles, functional annotations, assembled genomes (optional) | Adequate sequencing depth for species-level resolution (e.g., > 5 Gb per sample), accurate taxonomic assignments | QIIME2/MetaPhlAn output, KEGG/GO functional annotations, raw reads |
| Epigenomic Profiling (ChIP-seq) | Peak calls (BED format), associated sample metadata | Peak call quality assessed by MACS2 score, signal-to-noise ratio, FRiP (Fraction of Reads in Peaks) > 0.05 | BED files of peak calls, IGV tracks, QC report including FRiP, peak distribution, and blacklist analysis |
Key Genomics Services Offered
- Next-Generation Sequencing (NGS) Library Preparation and Sequencing
- CRISPR/Cas9 Screening Services
- Single-Cell Genomics Analysis
- Genotyping and SNP Analysis
- Long-Read Sequencing and Assembly
- Metagenomics and Microbiome Analysis
- Epigenomic Profiling (ChIP-seq, ATAC-seq)
- RNA Sequencing (Total RNA, mRNA, small RNA)
Service Level Agreement For Genomics Core Facilities
This Service Level Agreement (SLA) outlines the expected response times and uptime guarantees for services provided by the Genomics Core Facility. It is designed to ensure reliable and timely access to critical genomics resources for researchers.
| Service Category | Response Time (Initial Contact) | Uptime Guarantee | Notes |
|---|---|---|---|
| NGS Library Prep & Sequencing | 2 business days for initial consultation/quote; 5 business days for project initiation confirmation | 95% scheduled instrument uptime (excluding planned maintenance) | Uptime excludes user-induced errors or sample quality issues. |
| Genotyping & SNP Analysis | 3 business days for project design consultation | 98% availability of genotyping platforms (excluding planned maintenance) | Sample throughput dependent on platform capacity. |
| Gene Expression Profiling (qPCR, RNA-Seq) | 2 business days for initial consultation/quote | 95% scheduled instrument uptime (excluding planned maintenance) | Data analysis support turnaround time provided per project. |
| Data Analysis & Bioinformatics Support | 3 business days for initial query response; project-specific turnaround times agreed upon during consultation | N/A (Support is personnel-based) | Focus on analysis of data generated by the core. |
| Shared Instrumentation Access | 1 business day for booking confirmation/troubleshooting request | 97% instrument availability (excluding planned maintenance) | Reservations required. User training may be a prerequisite. |
| Consultation & Project Planning | 2 business days for initial scheduling | N/A (Consultation is personnel-based) | Availability may vary based on staff workload. |
Scope of Services Covered
- Next-Generation Sequencing (NGS) library preparation and sequencing services.
- Genotyping and SNP analysis.
- Gene expression profiling (e.g., qPCR, RNA-Seq).
- Data analysis and bioinformatics support for core-generated data.
- Access to shared instrumentation and equipment.
- Consultation and project planning services.
Frequently Asked Questions
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