Featured features
Delivering limitless genetic interpretation capabilities to support faster insights, precise analysis, and scalable clinical workflows.
Manage Patients
User authentication, institutional management, password reset, and account deactivation.
Manage Users
Patient data management, VCF uploads, medical history, and full data view.
Variant Query
Genetic variant search, ACMG guideline reference, and variant data download.
Variant Report
ACMG-guided filtering, inheritance visualization, variant interpretation, and report downloads.
Competitive Advantage
Our competitive advantage lies in combining AI-driven insights with user-centered design to deliver faster, more accurate, and scalable solutions.
About Us
Support local population studies!
SenusaBio excels in VUS classification and supports AI-driven local genetic interpretation.
Guaranteed Results
Provides automated variant reporting and interpretation features integrated with ClinVar and Ensembl databases.
Service Quality
The interpretation process is streamlined through the use of XAI and an ACMG-based Knowledge Base.
Testimonials
What Client says?
Frequently Asked Questions
Have Any Questions For Us?
We’d love to hear from you — have a question or need more information?
What is SenusaBio?
SenusaBio is a web-based application for genetic variant interpretation, locally developed by a team of bioinformaticians, researchers, and AI engineers in Indonesia. The platform follows international standards such as the ACMG Guidelines to assist in the analysis of inherited genetic disorders.
How is SenusaBio different from other genetic interpretation software?
SenusaBio is built to meet the unique needs of users in Indonesia. It offers:
- Full compliance with national data protection regulations (PDP Law, SATUSEHAT).
- Fast and secure processing for variant analysis.
- An intuitive, user-friendly interface.
- Locally supported development and integration with Indonesian health data frameworks.
How does SenusaBio work in variant interpretation?
SenusaBio analyzes variant data from VCF files following the ACMG Guidelines. The process is supported by AI, which automatically visualizes results and provides evidence-based classification. This includes population frequency, functional impact, in silico prediction, family segregation, and literature references.
Who can use SenusaBio?
SenusaBio is designed for a wide range of users, including:
- Genetic laboratories
- Hospitals and clinical researchers
- Universities and research institutions
- Professionals working in genomic and bioinformatics studies
- It can be applied in both research and clinical interpretation workflows.
Is patient data secure in SenusaBio?
Yes. SensuaBio applies multiple layers of data protection including encryption, hashing, masking, and access control. It fully complies with:
- Law No. 27/2022 on Personal Data Protection
- PMK 24/2022 (SATUSEHAT Regulation)
- PP No. 71/2019 on Electronic Systems
- and aligns with international standards such as ISO/IEC 27001.
Can SenusaBio be used for rare disease or cancer research?
Absolutely. SenusaBio has been utilized in both rare disease and cancer research projects at academic and hospital settings.
Key features include:
- Pedigree Drawer for visualizing family history alongside automated interpretation.
- Germline Variant Classification for identifying hereditary mutations.
- High concordance with other variant interpretation platforms.
Is SenusaBio available as a mobile app?
Currently, SENUSABIO is accessible via any web browser.
A mobile version is in development to improve accessibility and allow real-time monitoring of analyses and reports.
How can I request a demo or access SenusaBio?
You can contact the SENUSABIO team to schedule a demo session or discuss potential partnerships through the contact form on this website.
