Publications

We’re thrilled that so many researchers around the world have published their work using Kapa products. We’re in the last stage of launching our Publications Database of over 2600 articles, and hope to share it with you soon. In the meantime, check out some featured articles below.

For Research Use Only. Not for use in diagnostic procedures.

Development and validation of a clinical cancer genomic profiling test

Characterizing and measuring bias in sequence data

Optimal enzyme for amplifying sequencing libraries

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. Read the article here. 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. Read the article here. 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. Read the article here.
KAPA HiFi PCR KitsKAPA Library Quant Kits KAPA Library Prep Kits KAPA HiFi PCR Kits

Next-generation Sequencing

An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage

 

ChIP Sequencing

Automation of ChIP-Seq Library Preparation for Next Generation Sequencing on the epMotion® 5075 TMX

 

DNA Library Preparation

Characterizing and measuring bias in sequence data

 

Library Quantification

Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing

 

Methyl Sequencing

Ultra-low input, tagmentation-based whole-genome bisulfite sequencing

 

Sample QC

Importance of Reliable Quantification and Quality Assessment of Challenging FFPE Samples

 


qPCR

KAPA PROBE FAST

Molecular characterization of human T-cell lymphotropic virus type 1

 


PCR

KAPA Blood

Express barcodes racing from specimen to identification

 

KAPA2G Fast

Influence of PCR reagents on DNA polymerase extension rates measured on real-time PCR instruments

 

KAPA2G Robust

Improved efficiency and robustness in qPCR and end-point PCR

 

KAPA HiFi

Optimal enzymes for amplifying sequencing libraries

 

KAPA2G Fast Multiplex

Improving Lamda Red genome engineering in E. coli via rational removal of endogenous nucleases

 

KAPA3G Plant

Engineered DNA polymerase improves PCR results for plastid DNA