EasySeq™ Identification of Clinically and Biologically Relevant Genetic Mutations

Based on patented Reverse Complement PCR (RC-PCR) technology, providing simple and safer NGS Library Prep workflows combined with high assay sensitivity, EasySeq™ offers an ideal solution for public health, research, and precision medicine laboratories, even those lacking NGS experience.

To date, integration of targeted DNA capture and next-generation resequencing has been demonstrating to improve the ability to identify clinically and biologically relevant mutations. EasySeq™ NGS Library Prep by Reverse Complement PCR (RC-PCR) is the simplest, fastest and safest method for targeted DNA (re)sequencing of genes associated with cancers, cystic fibrosis and CFTR-related disorders.

A major challenge in complex sample handling and preparation workflows is the independent confirmation of the identity of multiple samples. In order to address this, NimaGen developed an EasySeq™ SNP genotyping assay with 36 intragenic high variable SNPs, facilitating an effective QA via straightforward sample tracking of WGS and WES data.

Our product portfolio includes:

.EasySeq™ Human Exome Sample Tracking Kit

.EasySeq™ CFTR Mutation Hotspot Sequencing Kit

.EasySeq™ CFTR Full Gene Sequencing Kit

.EasySeq™ BRCA1/2 + CHEK2 Full Gene Sequencing Kit

.EasySeq™ PALB2 Full Gene Sequencing Kit

.EasySeq™ TP53 Full Gene Sequencing Kit