enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  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. 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 ...

  5. List of Farm to Market Roads in Texas (2000–2099) - Wikipedia

    en.wikipedia.org/wiki/List_of_Farm_to_Market...

    Farm to Market Road 2093 (FM 2093) is located in Gillespie County in the Texas Hill Country. FM 2093 begins at an intersection with US 290 / RM 783 in Harper . The highway travels in a mostly eastern direction, passes through Tivydale, before entering Fredericksburg where the road ends at an intersection with SH 16 .

  6. DNA sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencing

    1 to 16 million Around 24 hours $667 Low-cost of instrument ($10,000) Chain termination (Sanger sequencing) 400 to 900 bp: 99.9%: N/A: 20 minutes to 3 hours: $2,400,000: Useful for many applications. More expensive and impractical for larger sequencing projects. This method also requires the time-consuming step of plasmid cloning or PCR.

  7. Single-cell transcriptomics - Wikipedia

    en.wikipedia.org/wiki/Single-cell_transcriptomics

    [16] When using RNA spike-ins for normalisation the assumption is made that the amplification and sequencing efficiencies for the endogenous and spike-in RNA are the same. Evidence suggests that this is not the case given fundamental differences in size and features, such as the lack of a polyadenylated tail in spike-ins and therefore shorter ...

  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. 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).