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  2. Massive parallel sequencing - Wikipedia

    en.wikipedia.org/wiki/Massive_parallel_sequencing

    Massive parallel sequencing or massively parallel sequencing is any of several high-throughput approaches to DNA sequencing using the concept of massively parallel processing; it is also called next-generation sequencing (NGS) or second-generation sequencing.

  3. DNA sequencing - Wikipedia

    en.wikipedia.org/wiki/DNA_sequencing

    The first of the high-throughput sequencing technologies, massively parallel signature sequencing (or MPSS, also called next generation sequencing), was developed in the 1990s at Lynx Therapeutics, a company founded in 1992 by Sydney Brenner and Sam Eletr. MPSS was a bead-based method that used a complex approach of adapter ligation followed by ...

  4. SNV calling from NGS data - Wikipedia

    en.wikipedia.org/wiki/SNV_calling_from_NGS_data

    SNV calling from NGS data is any of a range of methods for identifying the existence of single nucleotide variants (SNVs) from the results of next generation sequencing (NGS) experiments. These are computational techniques, and are in contrast to special experimental methods based on known population-wide single nucleotide polymorphisms (see ...

  5. Clinical metagenomic sequencing - Wikipedia

    en.wikipedia.org/.../Clinical_metagenomic_sequencing

    Clinical metagenomic next-generation sequencing (mNGS) is the comprehensive analysis of microbial and host genetic material (DNA or RNA) in clinical samples from patients by next-generation sequencing.

  6. RNA-Seq - Wikipedia

    en.wikipedia.org/wiki/RNA-Seq

    RNA-Seq (named as an abbreviation of RNA sequencing) is a technique that uses next-generation sequencing to reveal the presence and quantity of RNA molecules in a biological sample, providing a snapshot of gene expression in the sample, also known as transcriptome.

  7. 2 base encoding - Wikipedia

    en.wikipedia.org/wiki/2_Base_Encoding

    During sequencing, each base in the template is sequenced twice, and the resulting data are decoded according to this scheme. 2 Base Encoding , also called SOLiD ( sequencing by oligonucleotide ligation and detection ), is a next-generation sequencing technology developed by Applied Biosystems and has been commercially available since 2008.

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