Whole Exome Sequencing (Research)
Also known as: WES · Exome sequencing · Research exome
Subsidised whole exome sequencing for MSc, PhD and institutional research projects, with raw data delivery and optional bioinformatics support.
Reviewed by a certified medical doctor
This page and the corresponding laboratory report are overseen by an in-house clinician to ensure medical accuracy and patient safety.
- Reviewing doctorDr. Ibrahim Musa, MBBS, FMCPaed, Cert. Medical Genetics
- Clinical titleConsultant Medical Geneticist
- MDCN registrationMDCN/2011/58210
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Last clinical review
22 Jun 2026
Next review due 22 Jun 2027
“Access to sequencing should not be a barrier to Nigerian postgraduate research. Our subsidy programme is designed to make exome-scale data attainable for MSc and PhD candidates.”
Dr. Ibrahim Musa, MBBS, FMCPaed, Cert. Medical Genetics
When is this test recommended?
Intended for research use only, including:
- MSc and PhD thesis projects requiring exome-scale data
- Rare disease gene discovery studies
- Population genetics and genotype–phenotype research
- Institutional research requiring validated sequencing output
Not for clinical diagnosis unless commissioned as a validated clinical assay.
How to prepare and how the sample is collected
- Specimen typeEDTA whole blood or extracted DNA
- Turnaround21 business days
Patient preparation
For research use only. Submit a completed project abstract and institutional approval documentation where applicable.
Samples must be accompanied by proper chain-of-custody documentation and informed consent records.
Collection methods
- Painless cheek (buccal) swab — quick, non-invasive and suitable for all ages.
- Venous blood draw — EDTA whole blood, taken by a certified phlebotomist.
- Discreet home collection kit — courier-dispatched nationwide with clear instructions.
How your sample is analysed
Exome capture followed by next-generation sequencing on an Illumina-chemistry platform. Data is delivered as FASTQ/BAM/VCF. Optional bioinformatics support (alignment, variant calling, annotation) is available on request.
Platforms & instrumentation
Exome capture kits, Illumina-chemistry next-generation sequencing platforms, and validated secondary/tertiary bioinformatics pipelines.
- Documented standard operating procedures for every assay.
- Internal reference controls run alongside patient samples.
- Participation in external proficiency testing programmes.
- Dual-verification of every result before release.
How you receive your results
Encrypted, password-protected PDF report
Your results are delivered securely as an encrypted, password-protected PDF to your registered email address and WhatsApp. The file is never sent unprotected. Research data is delivered digitally in standard formats (FASTQ, BAM, VCF). Delivery is coordinated with the research supervisor and transferred securely.
Opening your report
- The PDF password follows a standard formula based on your personal details.
- Your counselor will confirm the exact password formula before release.
- Need help? Our team can re-issue or reset access on request.
Pre- and post-test counseling
Certified genetic counselors are available before and after your test to explain what the results mean, discuss implications for your family, and guide any next clinical steps.
Common questions about Whole Exome Sequencing (Research)
Yes. MSc and PhD candidates across Nigerian universities can apply for a research subsidy through our academic portal, subject to eligibility and project review.
By default this is a research-use assay. If you require clinically validated output, please request a clinical-grade assay commission at enquiry.
Standard bioinformatics formats: FASTQ (raw reads), BAM (aligned) and VCF (variants). Bioinformatics support is available on request.
Where to give your sample
Sample submission at Abuja, Lagos and Kaduna centres, or courier delivery of extracted DNA on request.