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  2. Nanopore sequencing - Wikipedia

    en.wikipedia.org/wiki/Nanopore_sequencing

    Another foundation for nanopore sequencing was the work of Hagan Bayley's team, who from the 1990s independently developed stochastic sensing, a technique that measures the change in an ionic current passing through a nanopore to determine the concentration and identity of a substance. By 2005 Bayley had made progress with the DNA sequencing ...

  3. Nanopore - Wikipedia

    en.wikipedia.org/wiki/Nanopore

    The observation that a passing strand of DNA containing different bases corresponds with shifts in current values has led to the development of nanopore sequencing. [14] Nanopore sequencing can occur with bacterial nanopores as mentioned in the above section as well as with the Nanopore sequencing device(s) is created by Oxford Nanopore ...

  4. Oxford Nanopore Technologies - Wikipedia

    en.wikipedia.org/wiki/Oxford_Nanopore_Technologies

    Oxford Nanopore Technologies plc is a UK-based company which develops and sells nanopore sequencing products (including the portable DNA sequencer, MinION) for the direct, electronic analysis of single molecules. [2] [3] [4] It is listed on the London Stock Exchange and is a constituent of the FTSE 250 Index. [5]

  5. Third-generation sequencing - Wikipedia

    en.wikipedia.org/wiki/Third-generation_sequencing

    Sequencing technologies with a different approach than second-generation platforms were first described as "third-generation" in 2008–2009. [4]There are several companies currently at the heart of third generation sequencing technology development, namely, Pacific Biosciences, Oxford Nanopore Technology, Quantapore (CA-USA), and Stratos (WA-USA).

  6. 16S ribosomal RNA - Wikipedia

    en.wikipedia.org/wiki/16S_ribosomal_RNA

    16S ribosomal RNA (or 16S rRNA) is the RNA component of the 30S subunit of a prokaryotic ribosome . It binds to the Shine-Dalgarno sequence and provides most of the SSU structure. The genes coding for it are referred to as 16S rRNA genes and are used in reconstructing phylogenies , due to the slow rates of evolution of this region of the gene ...

  7. Sanger sequencing - Wikipedia

    en.wikipedia.org/wiki/Sanger_sequencing

    [16] Sanger methods achieve maximum read lengths of approximately 800 bp (typically 500–600 bp with non-enriched DNA). The longer read lengths in Sanger methods display significant advantages over other sequencing methods especially in terms of sequencing repetitive regions of the genome.

  8. Nanopore battery - Wikipedia

    en.wikipedia.org/wiki/Nanopore_battery

    A nanopore battery is a rechargeable battery that is a composite of billions of nanoscale batteries formed within the pores of a substrate. [1] The space inside the holes is so small that billions of pores combined equal the volume of a grain of sand. Each pore's diameter was some one eighty-thousandth the width of a human hair. [1]

  9. Multilocus sequence typing - Wikipedia

    en.wikipedia.org/wiki/Multilocus_sequence_typing

    The Cronobacter MLST was initially applied to distinguish between C. sakazakii and C. malonaticus because 16S rDNA sequencing is not always accurate enough, and biotyping is too subjective. [10] The Cronobacter MLST scheme uses 7 alleles; atpD , fusA , glnS , gltB , gyrB , infB and ppsA giving a concatenated sequence of 3036 bp for phylogenetic ...