From Raw Data to Discovery and Publication
We bridge the gap between complex biological sequencing data and actionable discoveries. YaazhXenomics is your global partner for high-precision Genomic, Transcriptomic, Metagenomic, and Clinical Bioinformatics.
Why YaazhXenomics
Global Clientele — Serving research institutes, hospitals, and biotech firms worldwide. We seamlessly handle multi-national data requirements.
Uncompromised Security — Strict GDPR and HIPAA compliance for human genomic data. End-to-end encryption ensures your IP and patient data remain secure.
Secure Cloud Sharing — Fast, secure data transfer via AWS S3, Google Cloud, or enterprise-grade Aspera/SFTP servers. No data limits.
Fast Turnaround (TAT) — Our high-performance computing clusters and AI-optimized pipelines guarantee rapid delivery without compromising analytical depth.
Start Your Project Today
Our bioinformatics experts are ready to assist you. Contact us for a customized project quote, data transfer guidelines, or consultation. Send us your study objectives, sample count, and sequencing platform for an accurate estimate. Reach us at info@yaazhxenomics.com or +91-9500245454.
Our Core Multi-Omics Services
Explore our specialized analytical pipelines. Click on any service to view detailed methodologies, tools, deliverables, and pricing.
Whole Genome Assembly & Annotation
De novo and resequencing for Bacteria, Fungi, Plants, and Animals. High-quality contig generation and functional AI annotation.
Transcriptome Analysis (RNA-Seq)
Differential Gene Expression (DGE), isoform discovery, and comprehensive GO/KEGG pathway enrichment networks.
Metagenome Analysis
16S/18S/ITS diversity profiling and Shotgun functional pathway analysis. Discover novel strains and AMR genes.
Whole Exome Analysis (WES)
High-depth clinical exome sequencing analysis for rare Mendelian diseases and paired Tumor-Normal somatic calling.
Human Whole Genome (hWGS)
Uncover deep intronic variants, complex structural rearrangements (SVs), and comprehensive clinical reporting.
Pharmacogenomics (PGx)
CPIC-compliant reporting. Accurate Star Allele calling, HLA typing, and pseudogene resolution for precision medicine.
Transparent estimates for our analytical pipelines. Final pricing is tailored based on sequencing platform, coverage depth, and cohort size.
Service Base Pricing & Turnaround
Starting prices in INR by service category, complexity, and approximate turnaround time.
| Service Category | Complexity / Sample Type | Approx. TAT | Starting Price (INR) |
|---|---|---|---|
| De Novo Assembly | Microbial / Viral | 10-14 Days | ₹12,000 / Genome |
| De Novo Assembly | Plant / Animal (Complex) | 2-3 Weeks | Custom Quote |
| Resequencing | Microbial / Viral | 7-10 Days | ₹8,000 / Genome |
| Resequencing | Plant / Animal (Complex) | 1-2 Weeks | ₹15,000+ / Genome |
| Transcriptomics | Standard DGE & Pathway Analysis | 14-21 Days | ₹8,000 +/ Sample |
| Metagenomics | 16S/18S/ITS Diversity Profiling | 3-5 Days | ₹3,500 / Sample |
| Whole Exome (WES) | Research & Clinical Variant Calling | 1-2 Days | ₹5,500 / Sample |
| Human WGS | Germline / Tumor-Normal Pair | 4-8 Days | ₹15,000 / Sample |
| Pharmacogenomics | Array to Targeted Long-Read Panels | 2-4 Days | ₹7,500 / Sample |