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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. Shotgun sequencing - Wikipedia

    en.wikipedia.org/wiki/Shotgun_sequencing

    The classical shotgun sequencing was based on the Sanger sequencing method: this was the most advanced technique for sequencing genomes from about 1995–2005. The shotgun strategy is still applied today, however using other sequencing technologies, such as short-read sequencing and long-read sequencing.

  4. Primer walking - Wikipedia

    en.wikipedia.org/wiki/Primer_walking

    In contrast to directed sequencing, shotgun sequencing of DNA is a more rapid sequencing strategy. [6] There is a technique from the "old time" of genome sequencing. The underlying method for sequencing is the Sanger chain termination method which can have read lengths between 100 and 1000 basepairs (depending on the instruments used).

  5. DNA sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencing

    Sanger sequencing is the method which prevailed from the 1980s until the mid-2000s. ... The success of any DNA sequencing protocol relies upon the DNA or RNA sample ...

  6. COLD-PCR - Wikipedia

    en.wikipedia.org/wiki/COLD-PCR

    Comparison of Sanger sequencing chromatograms indicated that the mutant allele was enriched 13 fold when COLD-PCR was used compared to traditional PCR alone. [1] This was determined by the size of the peaks on the chromatogram at the variant allele location. As well, COLD-PCR was used to detect p53 mutations from lung-adenocarcinoma samples ...

  7. Dideoxynucleotide - Wikipedia

    en.wikipedia.org/wiki/Dideoxynucleotide

    Dideoxynucleotides are useful in the sequencing of DNA in combination with electrophoresis.A DNA sample that undergoes PCR (polymerase chain reaction) in a mixture containing all four deoxynucleotides and one dideoxynucleotide will produce strands of length equal to the position of each base of the type that complements the type having a dideoxynucleotide present.

  8. Philip J. Quigley - Pay Pals - The Huffington Post

    data.huffingtonpost.com/paypals/philip-j-quigley

    From January 2008 to December 2012, if you bought shares in companies when Philip J. Quigley joined the board, and sold them when he left, you would have a 12.1 percent return on your investment, compared to a -2.8 percent return from the S&P 500.

  9. Transcriptomics technologies - Wikipedia

    en.wikipedia.org/wiki/Transcriptomics_technologies

    In the 1980s, low-throughput sequencing using the Sanger method was used to sequence random transcripts, producing expressed sequence tags (ESTs). [2] [14] [15] [16] The Sanger method of sequencing was predominant until the advent of high-throughput methods such as sequencing by synthesis (Solexa/Illumina).