Sanger
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Sanger Sequencing Services
Gold-Standard. Accuracy. Tailored.
Sanger Sequencing remains the gold standard for accuracy when you need to verify specific genetic sequences. Whether you are confirming a single mutation or validating a synthetic construct, our service provides the high-resolution data necessary for definitive results.
- Plasmid & PCR Product Sequencing: Rapid turnaround for standard templates with high-confidence base calling.
- Mutation Detection: Ideal for identifying “hotspot” mutations, SNPs, and small indels with 99.9% accuracy.
- Primer Walking: Comprehensive sequencing of long DNA fragments (up to several kb) through iterative primer design and data assembly.
- Custom Sequencing Projects: Tailored workflows for difficult templates, including GC-rich regions or hairpin structures.
Nanopore
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Nanopore Sequencing Services
Real-Time. Long-Reads. Insights.
Our Nanopore platform offers a revolutionary approach to genomics by providing ultra-long reads in real-time. This is the ideal solution for researchers looking to map complex structural variants or assemble entirely new genomes from scratch.
- Rapid Results: Real-time data processing means you get actionable insights faster than traditional methods.
- Long-Read Capability: Sequence fragments from 10 kb to over 100 kb, allowing you to bridge repetitive regions and close genomic gaps.
- Direct RNA Sequencing: Skip the cDNA bias. We sequence native RNA strands directly to observe base modifications and poly-A tail lengths.
- Structural Variant Detection: Unrivaled sensitivity for detecting large inversions, translocations, and duplications.
NexoSeq NGS
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NexoSeq Next-Generation Sequencing (NGS) Services
High-Throughput. Precision. Discovery.
When your project demands massive scale, our NGS services deliver billions of data points with industrial-grade reliability. We specialize in deep sequencing that uncovers the hidden complexities of whole genome, transcriptome and exome.
- High-Fidelity Data: Leveraging advanced bridge amplification and “sequencing by synthesis” to provide high quality data consistently.
- Whole Genome & Exome Sequencing: Comprehensive coverage for identifying rare variants and conducting population-scale studies.
- RNA-Seq (Transcriptomics): Precise quantification of gene expression and identification of novel isoforms or splice variants.
- Metagenomics: Characterize entire microbial communities from environmental or clinical samples without the need for culturing.
| Feature | Sanger Sequencing | Nanopore Sequencing | NexoSeq NGS |
| Best For | Single-gene validation | Structural variants & De novo assembly | Large-scale discovery & RNA-Seq |
| Read Length | ~600 bp | 10 kb – 100 kb+ | 150 – 300 bp (Paired-end) |
| Throughput | Low (Single samples) | High | Ultra-High (Billions of reads) |
| Key Advantage | Gold-standard accuracy | Real-time / Long-reads | Lowest cost per base |
Why Choose Our Service?
Expert Support: Direct access to our genomic specialists for troubleshooting and data interpretation.
Unmatched Accuracy: Single-base resolution that ensures your discovery is built on a solid foundation.
Read Lengths: Consistently achieving high-quality reads of different lengths of DNA samples.
Rapid Turnaround: Data delivered via our secure portal within 24 hours of sample receipt.
NexoSeq NGS: Longer turnaround time, data analysis by NGS bioinformatics experts.