• Illumina NovaSeq & NextSeq – Gold-standard high-throughput short-read sequencing for deep coverage, excellent for WGS, exome, RNA-Seq, metagenomics, and large cohorts.
• Oxford Nanopore – Real-time, long-read sequencing (up to Mb lengths) with up to 99% accuracy – ideal for de novo assembly, structural variants, full-length transcripts, and complex microbial genomes.
• MGI & Thermo Ion Platforms – Flexible, high-output options for rapid projects, gene expression, and targeted applications.

Our multi-platform approach ensures the best fit for your project – balancing read length, accuracy, throughput, and cost.

Comprehensive NGS Services at Yaazh Xenomics

Access end-to-end NGS solutions tailored to diverse research needs:

• Whole Genome Sequencing (WGS) – Human, microbial, plant, animal; de novo & resequencing for variant discovery, cancer mutations, inherited disorders.
• Whole Exome & Targeted Sequencing – Clinical exome, custom panels (cancer, rare diseases, cardiology) for coding variant identification.
• Transcriptome Sequencing (RNA-Seq) – Gene expression, differential analysis, novel transcripts, lncRNA/small RNA.
• Metagenome Sequencing – Shotgun & amplicon (16S/18S/ITS) for microbiome, environmental, gut health, pathogen detection.
• Epigenome Sequencing – Bisulfite, methylation profiling to study environmental/lifestyle impacts on gene regulation.
• Medical & Clinical Genomics – Cancer panels, pharmacogenomics (PGx), rare disease testing, hereditary screening.
• Other: ChIP-Seq, single-cell, amplicon resequencing, FFPE-compatible NGS.

Our End-to-End NGS Workflow

1. Project Consultation – Free expert advice on design, platform selection, depth requirements, and budget optimization.
2. Sample Preparation & QC – High-quality DNA/RNA extraction from blood, tissue, FFPE, soil, water, low-input samples; rigorous QC.
3. Library Preparation & Enrichment – Optimized kits for target capture or whole-genome libraries.
4. High-Throughput Sequencing – Performed on state-of-the-art platforms with strict controls for uniformity and accuracy.
5. Advanced Bioinformatics Analysis (Free standard + custom):
   • Alignment, variant calling, assembly (short & long-read pipelines)
   • Annotation (ClinVar, gnomAD, KEGG, etc.), taxonomic/functional profiling
   • Custom reports: VCF, differential expression, pathway maps, visualizations
6. Data Delivery & Support – Raw FASTQ/BAM, processed files, detailed reports, post-delivery consultation for interpretation & publication.

Why Choose Yaazh Xenomics for NGS in India?

• Affordable & Transparent Pricing – Competitive rates with high value; superior quality at attractive prices for students, startups, and institutions.
• Fast Turnaround Time – Efficient workflows ensure rapid project completion without compromising data quality.
• Expertise & Reliability – Years of perfected NGS processes; ISO-certified labs with contamination controls and high success rates.
• Comprehensive Bioinformatics – Free basic analysis + advanced/custom pipelines for actionable, publication-grade insights.
• Nationwide Reach – Coimbatore HQ + Visakhapatnam branch; easy sample shipping/pickup across India.
• Diverse Applications – From microbial ecology and agriculture to clinical diagnostics and drug discovery.

Applications of Our NGS Services

• Academic & Life Science Research – Novel gene/variant discovery, phylogeny
• Clinical & Medical Genomics – Rare diseases, oncology, personalized medicine
• Agriculture & Environmental – Crop improvement, soil/water microbiome
• Pharma & Biotech – Biomarker identification, drug response studies
• Industrial Biotech – Probiotics, fermentation, enzyme engineering