In todays post, i will share an image that was taken today in my group. It is a pic of a computer screen (oh, how boring!!). What is it showcasing though? what do these color bars represent?

Firstly, I should say what the computer is hooked onto. The computer is connected to a MinIOn sequencing device (errrmmm a what?). Its one of the latest nucleotide sequencing techniques out there, developed by the company Oxford Nanopore.

https://steemitimages.com/DQmXEz2y1FW6yfcmgQ2nwsQc1s5NfnAJWwWPRssgsUe3gQ2/IMG_7276.JPG.jpeg

The image. A computer screen displaying a physical map of nanopores that are engaged in sequencing of a DNA sample. The color represents the status of each pore and the base that travels through it. This is a static image, if you were to film it, you would see the colors change constantly. Source: Own collection

Ok, so what does it do then?

Good question. In molecular biology, we rely on the availability of sequences that specify the structure, composition and functions of the molecules we study. Without those sequences, molecular biology would not exist or practicing in this field would become impossible. We therefore like to sequence the organisms we study. Initially and in the early days, this meant sequencing gene after gene, basepair by basepair. Technological advantages however have allowed us to scale this up significantly, allowing us to sequence complete genomes by generating short sequences (billions) that are assembled into one or more theoretical sequences. Rather then sequencing billions of short fragments, this device allows us to sequence a smaller number of larger molecules, circumventing this massive assembly challenge.

How is it different from other sequencing technologies?

Firstly, the chemistry and approach are completely different. Classical and next generation sequencing approaches all rely on the synthesis of DNA molecules and incorporation of modified nucleotides (each nucleotide having a different color). Incorporation of these bases allows very sensitive detectors to identify each incorporated base and read the sequence in this way. This technology is different as it does not rely on synthesis and incorporation of nucleotides. Rather, small pores (nanopores) made of proteins, are employed in the MinIon device that capture single DNA molecules and pass them through the pore. Whilst the DNA molecule travels through a charged pore, each base that passes can give a specific electric signature signal, which sensors can pick up and use to generate a base signal (also called a squiggle). These are then analyzed to determine what the identity of each base is and generate a sequence (base calling). Since there is not a synthesis requirement, very long molecules can be guided through these pores, leading to very long sequences that do not need to be assembled too much (theoretically). It also means that native DNA and RNA molecules can be sequenced including their possible modification (for example, see Simpson et al., 2017), something that other technologies cannot do.

Figure 1. Nanopore MinIon device. Source

As with most technologies, there are limitations. At this stage in the game, the accuracy of the device needs improvement (it makes base calling errors), but in combination with other more accurate sequencing technologies, this device allows rapid sequencing of full bacterial and eukaryote genomes as described in Loman et al., 2015; Goodwin et al., 2015; Debladis et al., 2017). There is little question though that this technology will change the face of biology. Accessibility to this device is far greater (i have it in my laboratory) then those super expensive Illumina or PacBio sequencers. Allowing biologists to conduct their own genome sequencing and analyses projects in house.

Research in Molecular Biology becomes ever more exciting (and challenging if you wish to keep up!!)

REFERENCES:

Debladis, E., Llauro, C., Carpentier, M. C., Mirouze, M., & Panaud, O. (2017). Detection of active transposable elements in Arabidopsis thaliana using Oxford Nanopore Sequencing technology. BMC genomics, 18(1), 537.

Goodwin, S., Gurtowski, J., Ethe-Sayers, S., Deshpande, P., Schatz, M. C., & McCombie, W. R. (2015). Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genome. Genome research, 25(11), 1750-1756.

Loman, N. J., Quick, J., & Simpson, J. T. (2015). A complete bacterial genome assembled de novo using only nanopore sequencing data. Nature methods, 12(8), 733-735.

Simpson, J. T., Workman, R. E., Zuzarte, P. C., David, M., Dursi, L. J., & Timp, W. (2017). Detecting DNA cytosine methylation using nanopore sequencing. nature methods, 14(4), 407-410.

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