Enzyme solutions for PCR, Real-Time PCR,
and Next-Generation Sequencing.
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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.
I would recommend the KAPA hgDNA Quantification and QC Kit to all CAP/CLIA labs and cancer testing centers because it is the most robust solution for screening both quantity and quality of sample material.