Our model is the most advanced ever made for gene assessment.
Manage Patients
The Manage Patients feature simplifies the organization and tracking of patient genetic data. Users can store medical records, manage IDs, status, disease history, and upload VCF files containing genome reference, sample date, and variant count. With tools for viewing, analyzing, and managing variant data, this feature supports genomic assessment, accurate diagnosis, and clinical decision-making.
Variant Report
The Variant Report Manager is an advanced tool for analyzing patient VCF files, allowing precise filtering of key genetic data like GENE ID, SYMBOL, Clinical Significance, Zygosity, and ACMG Classification. It enables users to extract insights, make informed interpretations, and generate recommendations based on genetic profiles. The final report can be exported in PDF, JSON, or XML formats for further evaluation and clinical decisions.
Variant Query
The Variant Library serves as a centralized repository for managing and accessing curated genetic variant data. It streamlines organization, retrieval, and comparison of analyzed variants, enhancing genomic research and clinical decision-making with accuracy and consistency.
Acknowledgment
This research project is funded by PT Biogenome Total Solusi and Universitas YARSI, with project Grant Number 023/SK/BTSS/I/24 and 0001/FTI/PKS HK.20/II/2024.
