Next-generation sequencing has facilitated the trend towards clinically-focused sequencing, but NGS sample preparation remains a bottleneck. What approaches can address the need for ever-higher sample throughput, quality, and reliability for NGS?
Sample prep can have a big impact on next-generation sequencing (NGS) outcomes. Here are some simple things you can do to get your NGS off to a good start.
Drilling down to the single-cell level provides insights into complex biological systems and diseases. Learn about single-cell sequencing, its applications and challenges.
As next-generation sequencing (NGS) makes inroads into clinical applications such as cancer diagnostics, we look at some of the NGS initiatives and collaborations aiming to change the landscape of clinical sequencing and improve patient’s lives.
GenomiPhi HY DNA Amplification Kit offers highly efficient and representative whole-genome amplification with 40 to 50 μg yield from nanogram amounts of DNA sample.
This kit combines the unique capabilities of Phi29 DNA polymerase with an optimized formulation to amplify genomic DNA from 1-1000 cells without background interference.
Efficiently prepare DNA sequencing templates from circular DNA.
This kit offers highly efficient and representative whole-genome amplification with 12 to 20 μg yield from nanogram amounts of DNA sample.