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  2. Pore-C - Wikipedia

    en.wikipedia.org/wiki/Pore-C

    Pore-C workflow. Many methods to characterize the 3D genome are variations on 3C technology. [5] Like other 3C-based technologies, [5] Pore-C seeks to characterize the architecture of the 3D genome by determining which genomic loci are in close spatial proximity (within ~200 nm). [2]

  3. 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 ...

  4. 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.

  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. Ribosomal intergenic spacer analysis - Wikipedia

    en.wikipedia.org/wiki/Ribosomal_intergenic...

    By using oligonucleotide primers targeted to conserved regions in the 16S and 23S genes, RISA fragments can be generated from most of the dominant bacteria in an environmental sample. While the majority of the rRNA operon serves a structural function, portions of the 16S-23S intergenic region can encode tRNAs depending on the bacterial species.

  7. 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 ...

  8. 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 ...

  9. DNA nanoball sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_nanoball_sequencing

    Workflow for DNA nanoball sequencing [1]. DNA nanoball sequencing is a high throughput sequencing technology that is used to determine the entire genomic sequence of an organism.