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NGS
Cost-efficient RNA Sequencing
Do you perform (or plan to) RNA Seq in your project? We know RNA sequencing can be complex, but you’re not alone. We’re here to support you at every stage of your workflow, whether it’s consultation, extraction, library preparation, or NGS services. |
Gene Expression Profiling: Save up to 10x cost per sample
- Save costs up to 90%: Sequence less reads than mRNA-Seq approaches without compromising data.
- Any sample: Low input samples, degraded samples, or blood.
- Scale up your experiments to 36,864 samples.
- Read more here.
Almost 100% genes detected from a single cell
- Obtain a clean and pure RNA library.
- Maximum sensitivity: amplifies RNA, not cDNA.
- Low input samples: from 1-100 cells.
- Read more here.
Whole Transcriptome Sequencing: One for all
- Save time: Workflow in only 4.5 hours.
- Protect your sample: Fragmentation-free method
- Best performance in low input samples: down to 1 ng starting amount.
- Read more here.
