Zist Kavosh Hooshmand combines next-generation sequencing, bioinformatics and machine learning to deliver precise genetic answers for clinicians and patients.
Order online, track samples and receive reports in a dedicated portal.
Explore genetic tests and timelines, and book a consultation.
We are a team of medical geneticists, biotechnologists and data scientists turning complex genomic data into actionable clinical reports.
From sample to report every step is checked against defined metrics and double review.
End-to-end encryption, anonymised IDs and informed consent for every patient.
Reproducible NGS analysis with fully versioned tools.
Smart variant prioritisation linking genotype to patient phenotype.
Follow your sample status in real time in the portal.
Our geneticists explain the result to physician and patient.
Sequencing of the protein-coding regions of the genome to identify the genetic cause of rare diseases, developmental disorders and more.
View detailsA complete view of the genome including coding and non-coding regions, structural variants and CNVs.
View detailsDisease-specific panels for cancer, cardiology, neurology, hearing loss and metabolic disorders with deep coverage.
View detailsPredicting drug response and tailoring dosage based on each patient’s genetic profile.
View detailsNGS data pipelines, variant calling, annotation and ACMG-based classification.
View detailsMachine-learning models for variant prioritisation and genotype–phenotype correlation.
View detailsAssess clinical needs and select the appropriate test.
Collect and ship the sample according to standards.
Prepare and sequence the sample using NGS technology.
Analyze data and prioritize genetic findings.
Deliver the final report through the doctors’ portal.
The portal makes your communication with the lab simple, transparent and trackable.
The reports are clear and the geneticists’ support in interpreting results was very helpful.
Online sample tracking and fast turnaround changed our clinic’s workflow.
Targeted panels are accurate and feedback from the analysis team is always fast and professional.
Specialist tutorials, practical projects and learning paths.
An example course with chapters and an editable playlist of real lesson, video, project and quiz pages.
Open content →A step-by-step route from FASTQ basics to a hands-on project and quiz, drawing on existing academy content.
Open content →
ArticleCompare one-person, two-person and trio exome sequencing and understand how parental samples can improve genetic variant interpretation.
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ArticleLearn which sample types a laboratory may accept for clinical exome sequencing, and when family samples or special precautions are needed.
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ArticleWhat affects the turnaround time of whole-exome sequencing, from sample checks and sequencing to bioinformatics and clinical sign-off.
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ArticleA practical guide to the sections of a clinical WES report, variant nomenclature, ACMG classifications, secondary findings and follow-up.
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ArticleWhy a negative exome result does not rule out a genetic condition: coverage gaps, structural variants, repeats, mosaicism and interpretation limits.
Read moreUsually 2–5 ml of blood in an EDTA tube. A sampling guide is provided after you place an order.
Depending on the test, from a few days to 6 weeks, and sample status is trackable in the portal.
WES covers the coding regions and WGS the whole genome. A geneticist recommends the best option based on clinical findings.
Data is encrypted, stored under anonymised IDs and shared with your physician only with your consent.
Cost depends on the test. Use the consultation form to get a clear, accurate estimate.
Yes, after report delivery counselling with a geneticist is available in person or online.
Tell us about genetic tests and services. No payment or time selection is required; our team will contact you.
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