Metagenomics enables the assessment of microbial diversity and quantities within samples. While 16S rRNA gene identification at ~1500 bp is common, many modern sequencing methods use only a ~450 bp fragment, leading to inaccuracies. Oxford Nanopore’s long reading technology enhances species identification by reading the full 1500 bp gene, advancing the field. Metagenomic analyses offer extensive options for detailed exploration of diverse sample types or components

Whole genome analysis involves a thorough study of an organism’s entire genome and its functional genes. This method detects variants – differences from the reference genome – along with antimicrobial resistance genes, secondary metabolite genes, and virulence genes in the annotated genome. It also includes tools like alignment images, circular genome depictions, genome comparison with close subspecies, polymorphism tables.

Experience our Amplicon Sequencing Service—a tailored genetic analysis solution crafted to reveal precise insights from DNA or RNA samples. Through targeted amplification and sequencing of specific regions, we deliver focused, high-resolution data ideal for identifying mutations, uncovering genetic diversity, and tracing variations. Our state-of-the-art technology ensures precise outcomes, even with limited genetic material, enabling swift and cost-effective decision-making. Whether in medical advances or environmental exploration, our Amplicon Sequencing Service paves the way for efficient and impactful genetic analysis.

We offer comprehensive RNA-Seq analyses,  differential gene expression (DEGs), fusion gene discovery, and variant identification such as  SNVs and Indels. These evaluations are conducted by skilled bioinformaticians utilizing cutting-edge technology and top-tier algorithms. Our bioinformatics solution facilitates both a comprehensive overview and detailed exploration of your RNA data, highlighting expression patterns through heatmap and Principal Component Analysis (PCA). Addi tionally, enrichment analyses employing databases like KEGG, GO, DO, Reactome, and WikiPathways yield valuable insights into the functional implications of your RNA data.

With our customized pipeline for detection of SARS-CoV-2 based on Oxford Nanopore sequencing technology which utilizes the benefits of long reads. Our service aligns the reads to SARS-CoV-2 reference genome, calls variants, and generates a consensus genome sequence. It then determines lineage, clade and phylogenetic tree information of the sample using Pangolin and NextClade. All the information with its data and QC metric files gets summarized in one extensive html report for easy viewing.