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  2. Nanopore sequencing - Wikipedia

    en.wikipedia.org/wiki/Nanopore_sequencing

    Nanopore sequencing is a third generation [1] approach used in the sequencing of biopolymers — specifically, polynucleotides in the form of DNA or RNA. Nanopore sequencing allows a single molecule of DNA or RNA be sequenced without PCR amplification or chemical labeling.

  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. Third-generation sequencing - Wikipedia

    en.wikipedia.org/wiki/Third-generation_sequencing

    Third-generation sequencing (also known as long-read sequencing) is a class of DNA sequencing methods which produce longer sequence reads, under active development since 2008. [ 1 ] Third generation sequencing technologies have the capability to produce substantially longer reads than second generation sequencing , also known as next-generation ...

  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. 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.

  7. Base calling - Wikipedia

    en.wikipedia.org/wiki/Base_calling

    Base calling is the process of assigning nucleobases to chromatogram peaks, light intensity signals, or electrical current changes resulting from nucleotides passing through a nanopore. One computer program for accomplishing this job is Phred , which is a widely used base calling software program by both academic and commercial DNA sequencing ...

  8. Today’s NYT ‘Strands’ Hints, Spangram and Answers for ...

    www.aol.com/today-nyt-strands-hints-spangram...

    Move over, Wordle, Connections and Mini Crossword—there's a new NYT word game in town! The New York Times' recent game, "Strands," is becoming more and more popular as another daily activity ...

  9. Sequence analysis - Wikipedia

    en.wikipedia.org/wiki/Sequence_analysis

    The tools used at this stage depend on the sequencing platform. For instance, FastQC checks the quality of short reads (including RNA sequences), Nanoplot or PycoQC are used for long read sequences (e.g. Nanopore sequence reads), and MultiQC aggregates the result of FastQC in a webpage format. [11] [12] [13]