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  2. Nanopore sequencing - Wikipedia

    en.wikipedia.org/wiki/Nanopore_sequencing

    The magnitude of the electric current density across a nanopore surface depends on the nanopore's dimensions and the composition of DNA or RNA that is occupying the nanopore. Sequencing was made possible because passing through the channel of the nanopore, the samples cause characteristic changes in the density of the electric current.

  3. Nanopore - Wikipedia

    en.wikipedia.org/wiki/Nanopore

    Schematic of Nanopore Internal Machinery and corresponding current blockade during sequencing. A nanopore is a pore of nanometer size. It may, for example, be created by a pore-forming protein or as a hole in synthetic materials such as silicon or graphene.

  4. DNA sequencer - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencer

    Oxford Nanopore Technologies' MinION sequencer is based on evolving nanopore sequencing technology to nucleic acid analyses. [37] The device is four inches long and gets power from a USB port. MinION decodes DNA directly as the molecule is drawn at the rate of 450 bases/second through a nanopore suspended in a membrane. [38]

  5. 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]

  6. RNA-Seq - Wikipedia

    en.wikipedia.org/wiki/RNA-Seq

    RNA-Seq has the potential to identify new disease biology, profile biomarkers for clinical indications, infer druggable pathways, and make genetic diagnoses. [ 151 ] [ 152 ] These results could be further personalized for subgroups or even individual patients, potentially highlighting more effective prevention, diagnostics, and therapy.

  7. 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).

  8. Pore-C - Wikipedia

    en.wikipedia.org/wiki/Pore-C

    Oxford Nanopore sequencing technology is costly, [12] and therefore Pore-C is more expensive per run when compared to other chromatin conformation capture techniques. Pore-C throughput is relatively low when compared to other techniques, particularly due to DNA-bound proteins clogging sequencing pores.

  9. FASTQ format - Wikipedia

    en.wikipedia.org/wiki/FASTQ_format

    FASTQ format is a text-based format for storing both a biological sequence (usually nucleotide sequence) and its corresponding quality scores.Both the sequence letter and quality score are each encoded with a single ASCII character for brevity.