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    SLAF-Seq

    生物信息分析
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      anneng 最后由 编辑

      c3780f1d-ab94-4a72-890f-128b323ea351-image.png
      Specific locus amplified fragment sequencing (SLAF-seq) is an optimized version of ddRADseq, specifically intended for large-scale genotyping experiments.

      The enzymes and the sizes of the restriction fragments are optimized with training data to ensure even distribution and avoid repeats. The fragments are also selected over a tight range, to optimize the PCR reaction. The protocol is similar to ddRAD, for example with a first digestion with MseI, heat inactivation and a second digestion with AluI. The resulting fragments are PCR amplified, adaptors added and the fragments purified.

      Pros:
      Deep sequencing for genotyping accuracy
      Reduced representation strategy to reduce sequencing costs
      Pre-designed reduced representation scheme to optimize marker efficiency
      Double barcode system for large populations
      Cons:
      Does not cover whole genome

      MseI
      f4f76e26-89cb-48fb-9ff2-44794159d724-image.png
      MseI, an isoschizomer of RspRSII, is a restriction enzyme that cleaves within the recognition sequence 5'-TTAA-3'.

      AluI
      77d49327-927e-4480-ad3a-201defc4cd7d-image.png

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