NGS library preparation. Evolved.
Researchers at Foundation Medicine have created a test to interrogate base substitutions, indels, copy number alterations and selected fusions across 287 cancer related genes from FFPE tumor samples using massively parallel next generation sequencing.
Researchers at the Broad Institute evaluate four sequencing platforms using human and microbial samples to assess sources of bias in sequencing and sample preparation workflow processes.
Researchers at the Sanger Center investigate many thermostable DNA polymerases along with various reaction conditions for adapter-ligated fragments for Illumina Sequencing in efforts to determine and reduce bias.
If you want to have tight control over your assay performance and save time and money, you need to set the standard up front. The KAPA hgDNA Quantification and QC Kit provides us with a way to determine how a sample will perform in an assay and understand how the DNA is going to behave.