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  2. Nanopore sequencing - Wikipedia

    en.wikipedia.org/wiki/Nanopore_sequencing

    This sequencing method has a capacity of 50-250 bases per second per pore, and a four color fluorophore system (each base could be converted to one sequence instead of two), will sequence over 500 bases per second. [36] Advantages of this method are based on the clear sequencing readout—using a camera instead of noisy current methods.

  3. DNA sequencer - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencer

    The sequencing methods applied by these sequencers do not require DNA amplification (polymerase chain reaction – PCR), which speeds up the sample preparation before sequencing and reduces errors. In addition, sequencing data is collected from the reactions caused by the addition of nucleotides in the complementary strand in real time.

  4. Single-molecule real-time sequencing - Wikipedia

    en.wikipedia.org/wiki/Single-molecule_real-time...

    The DNA sequencing is done on a chip that contains many ZMWs. Inside each ZMW, a single active DNA polymerase with a single molecule of single stranded DNA template is immobilized to the bottom through which light can penetrate and create a visualization chamber that allows monitoring of the activity of the DNA polymerase at a single molecule level.

  5. Single-cell sequencing - Wikipedia

    en.wikipedia.org/wiki/Single-cell_sequencing

    Nanopore-based sequencing also offers a route for direct methylation sequencing without fragmentation or modification to the original DNA. Nanopore sequencing has been used to sequence the methylomes of bacteria, which are dominated by 6mA and 4mC (as opposed to 5mC in eukaryotes), but this technique has not yet been scaled down to single cells ...

  6. DNA nanoball sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_nanoball_sequencing

    Bioinformatic mapping of the sequencing reads is most efficient when the sample DNA contains a narrow length range. [7] For small RNA sequencing, selection of the ideal fragment lengths for sequencing is performed by gel electrophoresis; [8] for sequencing of larger fragments, DNA fragments are separated by bead-based size selection. [9]

  7. 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 ...

  8. 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]

  9. Reduced representation bisulfite sequencing - Wikipedia

    en.wikipedia.org/wiki/Reduced_representation_bi...

    Only a low sample concentration, between 10-300 ng, is required for accurate data analysis. [2] This technique can be employed when there is a lack of precious sample. Another positive aspect is that fresh or live samples are not required. Formalin-fixed and paraffin-embedded inputs can also be used. [2]

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