MinION from Oxford Nanopore Technologies: the portable sequencing revolution
The MinION from Oxford Nanopore Technologies is a DNA/RNA sequencer that pushes the boundaries of genomic analysis with its ultra-portable format and high-performance technology. This compact device, weighing just 100 grams and fitting in the palm of your hand, stands out for its ability to perform real-time sequencing by simply connecting to a computer via a USB 3.0 port. Designed for researchers and professionals who want to combine performance, mobility and ease of use, the MinION provides access to valuable genetic data in a variety of settings, from laboratories to expedition sites.
This sequencer is based on nanopore technology, which detects current variations when DNA or RNA molecules pass through a membrane, enabling direct and continuous reading of sequences. The MinKNOW software that accompanies the MinION offers complete process management: device control, data acquisition, real-time analysis and automatic conversion to standard formats such as FASTQ or BAM. This ability to analyse samples as they are sequenced saves researchers considerable time and facilitates rapid decision-making.
The MinION is designed to work with different flow cells, including classic flow cells for large-scale sequencing and Flongle adapters for applications requiring lower throughput, making the platform extremely versatile. Integrated temperature control (operating between 18°C and 25°C) ensures optimal conditions for experiment stability and performance. Precise LED indicators provide the user with visual feedback on the status of the device and the progress of sequencing.
In addition to its use in the laboratory, the MinION is invaluable for field applications such as environmental monitoring, pathogen identification and rapid biodiversity studies. Its ability to produce long reads makes it particularly suitable for the study of complex genomes, complete transcripts and epigenetic modifications.
With MinION, Oxford Nanopore Technologies provides researchers with a flexible, powerful and easy-to-use tool that opens up new possibilities in genome sequencing worldwide.
