Genotypic Sequencing Services
Features
Flexible
Run upto 5 Flongle or MinION flow cells individually or together
High Throughput
Generate as much as 250 GB data in 72 hours
Real-Time
Simultaneous data streaming for immediate interpretation
Capitalize
Allows users to offer nanopore sequencing as a service
Ultra Long Read
Generate from small to ultra-long reads
Integrated Compute System
Sequencing and analysis in one system
Applications
- Larger genomes or projects
- Whole transcriptomes (direct RNA or cDNA)
- Large numbers of samples
- Whole genomes/exomes
- Metagenomics
- Targeted sequencing
- Disease outbreak study
- Epigenetics
Launching High Throughput Sequencing Services Using Nanopore PromethION
The Promethion provides live high accuracy base-calling at low cost and low TAT, alignment and methylome calls can also be done while sequencing. This opens up new possibilities for Nanopore minion users as well as for short read users. Genotypic will be presenting the work flows for CfDNA, WGS metagenome and large genome sequencing projects – in Human genetics to Agriculture and Biopharma.
Modular
Run upto 48 flow cells together or individually
High Throughput
Yields up to 11 Tb in 48 hours for the whole device.
Real-Time
Integrated compute for real-time base calling and onward analysis.
Large-Scale Sequencing
Generate robust data for large projects
High accuracy base calling Q30+ duplex reads
High accuracy and ultra long reads ensure you get the best quality genomes for all your biological experiments! You can now have the Power of calling SNVs, CNVs Indels, Structural Variations & Methylation – all from the same data!
- WGS of Larger genomes (Plants/Humans/Bovines)
- Whole Genome Metagenome Sequencing
- Transcriptome Sequencing
- DNA/RNA Modifications (Methylation/Acetylation)
- Quick TAT : 24 flowcells 120GB x 24 run in parallel
- Live alignment
Applications
- Larger genomes or projects
- Population-scale sequencing
- Highly multiplexed small genomes or targeted regions
- Whole transcriptomes (direct RNA or cDNA)
- Whole genomes/exomes
- Metagenomics
- Targeted sequencing
- Disease outbreak study
- Epigenetics