Full-length 16S (V1-V9), Direct RNA Sequencing, Long-read Transcriptomics, WGS, Plasmid, Virus & Phage with complete end-to-end bioinformatics.
Reads exceeding 4 Mb enable complete microbial genomes, resolve complex repeats, structural variants, and full plasmids.
Live data streaming with MinKNOW + EPI2ME. Ideal for rapid pathogen detection and time-critical projects.
Sequence native DNA or RNA without PCR bias. Directly detect base modifications such as methylation.
We operate the latest Oxford Nanopore platforms with high-accuracy chemistry (R10.4.1 / Kit 14).
Ideal for rapid response, small-to-medium projects, and on-site or remote sequencing.
Up to 5 flow cells simultaneously. Perfect balance of throughput and flexibility.
High-capacity platform ideal for large-scale transcriptome sequencing, deep metagenomics, and high-sample-number projects.
Complete ~1.5 kb 16S rRNA gene sequencing for superior species and strain-level taxonomic resolution.
Native RNA sequencing without cDNA conversion. Capture full-length transcripts, isoforms, and RNA modifications in real time.
High-resolution profiling of microeukaryotes and protists using the complete 18S gene.
Full or near-full COI gene sequencing for accurate animal, insect, and invertebrate species identification.
Long-read sequencing of fungal LSU rRNA genes for precise yeast and filamentous fungi identification.
De novo assembly of bacterial, viral, fungal, and small eukaryotic genomes with superior resolution of repeats and structural variants.
Rapid full plasmid sequencing, complete viral genomes, and phage sequencing for research and phage therapy development.
From raw reads to publication-ready insights with expert analysis and comprehensive deliverables.
World-class long-read sequencing and deep bioinformatics at competitive Indian pricing with full transparency.
| Feature | Nanopore Long-Read | Short-Read (Illumina) |
|---|---|---|
| Read Length | 10 kb – >4 Mb | 150–300 bp |
| Full-length Transcript / Isoform Detection | Excellent | Limited |
| RNA Modification Detection | Native (Direct RNA) | Requires special methods |
| Structural Variants & Repeats | Excellent resolution | Poor |
| Real-time Results | Yes | No |
Get a customized quote and technical consultation from our genomics team within 24 hours.
Yaazh Xenomics is a leading biotechnology company based in Coimbatore, Tamil Nadu, India, specializing in comprehensive genomic solutions. As a DNA testing laboratory, we offer a broad spectrum of services, including DNA sequencing, RNA Sequencing, Sanger Sequencing, 16s rRNA, 18s rRNA, ITS, COI, RBCL, Matk gene Sequencing for DNA Barcoding, gene expression analysis, SNP analysis, Next-Generation Sequencing (NGS), Various Medical Genome testing, Exome Sequencing, Gut Microbiome Test, Metagenome Sequencing, Whole Genome Sequencing (WGS), Transcriptome Sequencing using advance NGS platforms like Nanopore, Illumina, MGI, Thermo. Also, we provide advance Bioinformatics, Customized Bioinformatics and a variety of other genetic testing and Molecular testing.