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  2. Sanger sequencing - Wikipedia

    en.wikipedia.org/wiki/Sanger_sequencing

    Microfluidic Sanger sequencing is a lab-on-a-chip application for DNA sequencing, in which the Sanger sequencing steps (thermal cycling, sample purification, and capillary electrophoresis) are integrated on a wafer-scale chip using nanoliter-scale sample volumes. This technology generates long and accurate sequence reads, while obviating many ...

  3. DNA sequencer - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencer

    The AB370A was able to sequence 96 samples simultaneously, 500 kilobases per day, and reaching read lengths up to 600 bases. This was the beginning of the "first generation" of DNA sequencers, [2] [3] which implemented Sanger sequencing, fluorescent dideoxy nucleotides and polyacrylamide gel sandwiched between glass plates - slab gels. The next ...

  4. DNA sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencing

    GenapSys Sequencing: Around 150 bp single-end 99.9% (Phred30) 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.

  5. Metabarcoding - Wikipedia

    en.wikipedia.org/wiki/Metabarcoding

    The Sanger method is limited and can produce a single read at the same time and is therefore suitable to generate DNA barcodes from substrates that contain only a single species. [30] Emerging technologies such as nanopore sequencing have resulted in the cost of DNA sequencing reducing from about USD 30,000 per megabyte in 2002 to about USD 0. ...

  6. DNA barcoding - Wikipedia

    en.wikipedia.org/wiki/DNA_barcoding

    DNA barcoding techniques were developed from early DNA sequencing work on microbial communities using the 5S rRNA gene. [11] In 2003, specific methods and terminology of modern DNA barcoding were proposed as a standardized method for identifying species, as well as potentially allocating unknown sequences to higher taxa such as orders and phyla, in a paper by Paul D.N. Hebert et al. from the ...

  7. Primer walking - Wikipedia

    en.wikipedia.org/wiki/Primer_walking

    Primer walking is a method to determine the sequence of DNA up to the 1.3–7.0 kb range whereas chromosome walking is used to produce the clones of already known sequences of the gene. [2] Too long fragments cannot be sequenced in a single sequence read using the chain termination method. This method works by dividing the long sequence into ...

  8. Sequencing - Wikipedia

    en.wikipedia.org/wiki/Sequencing

    DNA sequencing is the process of determining the nucleotide order of a given DNA fragment. So far, most DNA sequencing has been performed using the chain termination method developed by Frederick Sanger. This technique uses sequence-specific termination of a DNA synthesis reaction using modified nucleotide substrates.

  9. Gene Codes Corporation - Wikipedia

    en.wikipedia.org/wiki/Gene_Codes_Corporation

    Gene Codes Corporation is a privately owned international firm based in Ann Arbor, Michigan, which specializes in bioinformatics software for genetic sequence analysis.Its flagship software product, Sequencher, is a sequencing software used throughout the world.

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