TruSeq Nano DNA

TruSeq Nano DNA

简单、一切全包的制备方案,适合全基因组测序。这个新的流程需要较少的DNA投入量,能够拷问DNA有限的样品,同时带来了出色的基因组覆盖度和均一性。
LT方案有Set A和Set B可供选择。每组包含12个独特的索引,可合并在一起实现24重的分析。

Simple, all-inclusive prep solution, ideal for whole-genome sequencing. This new workflow offers reduced DNA input allowing for interrogation of samples with limited available DNA while providing excellent genomic coverage and uniformity.
The HT option provides dual index combinations for up to 96plex.

The TruSeq Nano DNA for NeoPrep offers a simple, all-inclusive prep solution, ideal for any whole-genome sequencing application. Run the same proven TruSeq Nano DNA biochemistry on the fully integrated digital microfluidics NeoPrep Library Prep System. The NeoPrep System significantly simplifies library preparation, delivering highly reproducible, sequencing-ready libraries of superior data quality and genomic coverage with minimal hands-on time.

LT HT NeoPrep

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* 文库制备与Illumina所有仪器兼容。建议仪器是根据所选应用的典型产量和分析需求选择的。
† 建议的下游分析
项目建议
物种兼容性 与大多数大型基因组DNA兼容
建议的Illumina仪器* NextSeq 500 HiSeq 2500 (双流动槽)
每次运行建议的样品数量 1 2-10
运行模式 中等产量 高产量 快速运行 高产量
建议的最长读长 350 bp 插入片段: ≤ 2x101 bp
550 bp 插入片段: ≤ 2x151 bp
350 bp 插入片段: ≤ 2x101 bp
550 bp 插入片段: ≤ 2x151 bp
350 bp 插入片段: ≤ 2x101 bp
550 bp 插入片段: ≤ 2x151 bp
350 bp 插入片段: ≤ 2x101 bp
550 bp 插入片段: ≤ 2x126 bp
建议的二次分析
  • BWA WGS BaseSpace App
  • Isaac WGS v2 BaseSpace App
  • SPAdes Genome Assembler
建议的下游分析 VariantStudio