Technologies

time icon June 9, 2017

Single-Step Method to Fragment and Tag Both Ends of DNA Molecules with Arbitrary Nucleotide Sequences

Technology description

Researchers in the Lewis-Sigler Institute for Integrative Genomics at Princeton University have developed a new simplified method to fragment and tag both ends of DNA molecules with arbitrary nucleotide sequences for Next Generation Sequencing as well as other high-throughput DNA processing.

This invention combines all reagents in a single step to fragment and tag both ends of DNA molecules with desired nucleotide sequences with optional PCR amplification, while all other existing NGS library preparation methods involve multiple steps which use different reagents.

This invention not only reduces the hands-on sample processing time, but also greatly facilitates the high-throughput compartmentalized DNA processing, such as water-in-oil emulsion droplets, which are not amenable to using different reagents in multiple steps. This invention can potentially be used in other types of compartmentalized micro-reactors and nano-biotechnologies.

Application area

• DNA library preparation for Next-Generation Sequencing
• Emulsion droplet based DNA processing
• Nano-biotechnologies and other micro-reactors on DNA

Advantages

• Simplest 1-step method
• Single reaction mixture including all reagents and DNA sample
• Reaction controlled by a series of incubation temperatures
• Reduced sample processing time
• Optional final PCR amplification

由于技术保密工作限制,技术信息无法完全展现,请通过邮箱或短信联系我们,获取更多技术资料。

More information

Institution
Categories
  • Information technology
  • Medical genetics
Keywords:

arbitrary nucleotide sequences

desired nucleotide sequences

optional pcr amplification

water-in-oil emulsion droplets

high-throughput dna processing

下载 PDF 文档


感兴趣

Contact us

知繁业茂-yintrust logo知繁业茂-Branchly Innovation logo 知繁业茂-autmasia logo迈科技 logo