Solutions for Translational and Clinical Researchers

Enzymatic fragmentation enables scalable preparation of high-quality FFPE libraries with minimal artifacts

Customizing Watchmaker DNA PCR-free Library Prep Kit for Improved NovaSeq X Performance
As presented at ESHG 2024, in collaboration with SciLifeLab
(added September 6, 2024)

Non-invasive pre-natal testing: Embracing low-input methodologies
As presented at ESHG 2024, in collaboration with Trisomy Test, Ltd.
(added September 4, 2024)

A comparative analysis of library preparation technologies for RNA sequencing from FFPE samples

Optimized RNA Seq library preparation for fusion calling from FFPE samples

Overcoming sample quality and quantity limitations for NGS analysis of clinically relevant samples

Cost-effective, high-resolution whole transcriptome sequencing for gene fusion detection applications

Increasing Complexity and Quality of Total RNA Sequencing at Scale

Optimized enzymatic fragmentation workflow for the rapid construction of high-quality whole genome and whole exome libraries that is compatible with several blood collection methodologies