From genomics and transcriptomics to proteomics and metabolomics, experience unparalleled ease and efficiency.
The Future of Genetic Analysis Begins Here
PanOmiQ’s unified approach applies to whole-genome sequencing, whole exome sequencing and shotgun microbiome analysis, making it a versatile choice for all. Our state-of-the-art platform is designed meticulously to analyze diverse omic data sets in a matter of hours.
Researchers, clinicians, hospital personnel or diagnostic centers interested in analyzing genomic and metagenomics data, PanOmiQ is your solution.
One platform, countless possibilities!
PanDrugs Discovery: Empowering Researchers from Molecule to Mechanism
BioTalk: Talk to Your DNA to Unlock Genomic Intelligence with Conversation
PanOmiQ™: The Panther of Multiomics – Ultra-Fast Genomic Intelligence at Scale
The insights to optimization of genomics analysis process
We are living on the verge of an era of population-wide genomic analysis. Genomics plays a crucial role in pharmaceutical R&D and healthcare, providing insights into disease mechanisms, drug responses, and patient outcomes. A complication associated with this is the sheer volume and complexity of data.
Al algorithms can analyze large datasets quickly, identify patterns, and predict outcomes, enabling researchers to make more informed decisions from genomic insights with unmatched speed and accuracy.
PanOmiQ eliminates the need in complex bioinformatical models, enabling whole genome analysis to the broader spectrum of scientists and healthcare specialists
PanDrugs Discovery Platform: Empowering Researchers from Molecule to Mechanism
Integrated Intelligence for Computational Drug Discovery
Empowering Researchers from Molecule to Mechanism
In a landscape where drug discovery demands both precision and speed, the PanDrugs Discovery Platform emerges as a transformative in-silico suite which is meticulously crafted for pharmaceutical researchers, computational chemists, structural biologists, and academic scientists. Whether you’re a seasoned modeler or new to computational workflows, PanDrugs offers an intuitive, all-in-one solution to accelerate drug discovery from hypothesis to validation.
BioTalk: Talk to Your DNA to Unlock Genomic Intelligence with Conversation
The Future of Genomic Insight is Not in Code - It’s in Conversation
What if your genome could speak to you? What if complex genetic/metagenomic data, buried in PDFs or spreadsheets, could be explained in plain, simple and understandable terms personalized just for you? Welcome to BioTalk, a revolutionary AI-powered genomic assistant that transforms static DNA and microbiome reports into dynamic, meaningful dialogue. With a simple upload of a PDF or CSV file, BioTalk analyzes your genetic or microbiome data and enables a natural-language conversation with your own biology.
PanOmiQ™: The Panther of Multiomics – Ultra-Fast Genomic Intelligence at Scale
From Raw Data to Actionable Reports in Under 5 Minutes
In the race to bring precision medicine to the frontlines of healthcare, time is everything. Genomic analysis which was once a bottleneck has now entered a new era of speed, integration, and intelligence. At the forefront of this revolution stands PanOmiQ™, the world’s fastest multi-genomic platform. Capable of processing Whole Genome Sequencing (WGS) data in under five minutes, PanOmiQ delivers high-resolution insights at unprecedented speed. But this isn’t just about velocity; it’s about what that speed enables: real-time pharmacogenomics reporting, comprehensive microbiome profiling, and seamless multi-omics integration. With PanOmiQ, what once took hours or days can now happen during a coffee break.
Your Gateway to Smarter Drug Design
The PanDrugs Discovery Platform is more than software; it’s a scientific enabler. It bridges biology, chemistry, and computation in a unified space, helping researchers uncover insights faster, reduce experimental overhead, and design better therapeutics with confidence.In an era of complex diseases and precision medicine, PanDrugs positions your research at the forefront of innovation.
Key features & Capabilities
Automation at its peak
- Facilitates easy data upload for users.
- Automated analysis identifies rare diseases, health predispositions, and pharmacogenomic insights.
- Results are presented in a user-friendly, readable format for accessibility and comprehension.
COMPATIBLE FILE FORMATS & CUSTOMIZATION
- Compatibility with genetic file formats such as:
- FastQ
- VCF
- Customization options ensure no need for external software.
PARALLEL PROCESSING
- AI-driven software ensures efficient parallel processing.
- Automates the analysis pipeline to enhance speed and efficiency.
DIVERSITY OF DATA
- dbSNP (Single Nucleotide Polymorphism database)
- ClinVar (Clinical Variation database)
- ACMG (American College of Medical Genetics and Genomics)
- Orphanet (Rare Diseases database)
- OMIM
GENETIC DATA ACCURACY
- Committed to delivering precise results in identifying genetic variations.
DATA RELIABILITY
- Attention to detail ensures reliability.
- 98% coverage rate reflects thorough sequencing and completeness of genetic data.
QUANTUM - COMING SOON
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Latest News & Updates by PanOmiQ
Get In Touch
Experience the future of genetic analysis with PanOmiQ! Our innovative software is your all-in-one solution for omics analysis and reporting. Reach out today to discover how we’re revolutionizing genetic analysis with our cutting-edge platform.
