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cDNA Synthesis & Library Construction


Products >  cDNA_Synthesis_and_Library_Construction >  Next_Gen_Sequencing_Kits >  Featured_NGS_Kits

SMARTer NGS products

Expanding NGS portfolio

We are pleased to announce that we have recently merged with Rubicon Genomics. In addition to our existing SMARTer RNA-seq products, we now offer solutions for low-input DNA-seq for both whole genome and targeted sequencing applications. Some of our highlighted products are shown below, and our full product portfolio can be viewed by browsing our site.

Ultra-low mRNA-seq

  • Start with single cells or 10 pg–10 ng of total RNA input
  • Preserve sample integrity with single-tube processing
  • Get accurate representation of GC-rich transcripts

Low-input WTA

  • Start with 250 pg–10 ng of total RNA input
  • Work with high-quality, partially degraded, or low-quality samples
  • Generate Illumina-ready libraries in ~5 hours

Rare allele detection

  • Start with 1–50 ng of cell-free DNA or fragmented dsDNA
  • Detect rare alleles with unique molecular tags
  • Correct sequencing errors and reduce background

Low-input DNA-seq

  • Prep Illumina libraries from 50 pg–50 ng of input DNA
  • Start with FFPE, cDNA, or ChIP samples
  • Use with major target enrichment platforms

Single-cell WGA

  • Go from a single cell to a sequencing-ready library in just 3 steps
  • Detect low-frequency alleles, copy number variation, and aneuploidy

Other key applications

Immune profiling

Cell-free DNA-seq

Browse our complete DNA‑seq and RNA‑seq selection guides to find the right products for your research.

NGS resource portal

See more NGS resources:

  • Tech notes
  • Webinars
  • Scientific posters
  • FAQs
  • Tips
  • Citation lists
  • Product selection guide
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