History, habits and goals
The doctor reviews personal and family history, lifestyle, previous tests and questions about the test.
Accompanied genetic evaluation
NeoCheckup: genetic testing with follow-up.
The same genetic content as Longevo, with two medical consultations: one before the test and another after the report.
Not sure whether NeoCheckup is for you? Take the genetic history questionnaire
- Accepted samples
- Peripheral blood, Buccal swab (preferred), Extracted DNA
- Turnaround time and when it starts
- 20 calendar days, after acceptance of the sample
- Medical order
- Not required. View requirements and limitations.
Clinical journey
The examination begins before sample collection.
The pre-test consultation defines the relevant questions. After the analysis, the post-test consultation organizes what the result means for you and what the next steps are.
The same genetic content
The sample is collected with a mouth swab and goes through the same genetic analysis, specialized curation and preventive scope offered by Longevo.
Results in context
The post-test consultation explains findings, limitations and next steps in light of your history.
Same content as Longevo
More than 100 conditions evaluated.
NeoCheckup fully maintains the genetic analysis of Longevo: 155 genes, selected polygenic scores and pharmacogenomics. The difference is in the clinical journey before and after the test.
01
Hereditary cancer
Breast and ovarian, colorectal, prostate, endocrine tumors, melanoma and other predisposing syndromes.
02
Cardiovascular health
Cardiomyopathies, arrhythmias, aortic diseases, hereditary cholesterol and polygenic risk of heart attack.
03
Neurology and metabolism
Neurodegenerative, neuromuscular, metabolic, endocrine conditions and changes in iron metabolism.
04
Pharmacogenomics
Information on the response and metabolism of selected medications, including in mental health.
Medical follow-up
Clinical experience to interpret what matters.
Monitoring is carried out by Dr. João Bosco de Oliveira Filho, founder of NeoGenomica and a doctor with more than 20 years of experience in clinical genetics.
- Before the test
- Defining objectives and collecting clinical information.
- After the report
- Post-test consultation to explain findings, limitations and next steps.
Follow-up after your results
Infinity VUS
All NeoGenomica tests include Infinity VUS to follow reported variants of uncertain significance. When a relevant reclassification is confirmed after specialist review, the doctor is notified and the report may be updated.
Understand results and Infinity VUSAccompanied journey
From assessment to results.
An organized journey to link genetic data, history and prevention.
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01
Scheduling
The team confirms the service and guides the preparation for the evaluation.
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02
Pre-test consultation
The doctor reviews the history, objectives and questions before sample collection.
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03
Sample collection
The buccal swab is collected and sent to the laboratory with traceability.
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04
Genetic analysis
The DNA goes through the same genetic content and the same curation as Longevo.
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05
Results consultation
The report is put into context at the post-test consultation, with guidance on next steps.
Clinical feedback
Clarity about findings and limits.
The report brings together the results by clinical area. At the return visit, each finding is related to the history and follow-up recommendations.
- Summary of main findings.
- Analysis by health category.
- Points for prevention, tracking and referral.
Frequently asked questions
Before scheduling.
What is the difference between Longevo and NeoCheckup?+
The genetic content is the same. NeoCheckup adds a pre-test consultation and a post-test consultation.
Do I need a medical request?+
No. The initial assessment itself organizes the indication, objectives and information necessary for the test.
How are consultations carried out?+
The team informs you of the modality and availability when scheduling. The first consultation takes place before sample collection and the return after the report is released.
Does the result automatically change medications or screenings?+
No. The report generates information for clinical discussion. Changes in treatment, medication or screening depend on individual assessment.
Is the test covered by health insurance?+
The service is private. The team can provide documentation to request reimbursement when the plan contract allows.
When will the result be ready?+
20 calendar days, after acceptance of the sample. The follow-up consultation is scheduled after the report is released.
Clinical follow-up
Start with the conversation, not the report.
Schedule the pre-test consultation and understand how NeoCheckup relates your genetic data to your health history.
Test information
Technical details for NeoCheckup
Method, scope, requirements and limitations
The same content as Longevo, with pre- and post-test consultations.
- Applications
- Hereditary cancer, Personalized prevention, Cardiovascular risk, Pharmacogenomics
- Accepted samples
- Peripheral blood, Buccal swab (preferred), Extracted DNA
- Estimated turnaround time
- 20 calendar days, after acceptance of the sample
- Methodology
- Longevo's genetic content and curation, integrated with medical consultations before and after the test.
- Analytical scope
- 155 genes, selected polygenic scores and pharmacogenomics; pre- and post-test consultations.
- Medical order
- Not mandatory
Requirements
Does not require a medical request; the initial assessment organizes indication, objectives and necessary information. Home sample collection uses a mouth swab.
Limitations
Findings and scores must be interpreted in conjunction with history, habits, tests and goals of care.
Additional information
The genetic content is the same as Longevo; the difference is the medical consultations before and after the test.
