Free Webinar: Multiplexed Illumina Sequencing: Eliminating False Positives by Mitigating Sample Misalignment
Learn how to improve your NGS data reliability
Learn how to improve your NGS data reliability
Dr. Megan Allyse from the Mayo Clinic Center for Individualized Medicine explains why gene editing is not yet suitable for medical practice
An additional high-throughput Illumina NovaSeq 6000 is installed in Amsterdam as a result of increased demand for Macrogen’s sequencing services
Gain insights on topics from metabolomics to high-resolution genome libraries, CRISPR innovations advancing translational research, and more
SureSeq myPanel™ NGS Custom Cancer Panels enable researchers to create bespoke probe panels from an expert-curated library
The partnership will support agrigenomic laboratories and molecular breeders seeking to improve efficiency, increase throughput, and obtain high-quality DNA across diverse sample types
Thermo Fisher Scientific’s Ion S5 systems provide a single solution for the widest range of targeted sequencing applications
Dr. Bruce Conklin, UCSF, discusses the potential of genome engineering as a therapy for genetic diseases
Collaboration establishes high-quality sequence map based on Horizon’s GS Knock-Out CHO K1 cell line
Extended RAS Panel helps identify colorectal cancer patients eligible for Amgen’s Vectibix
The new RNA extraction kits include the SPINeasy RNA Kit for Tissue, the SPINeasy RNA Kit for Bacteria, and the SPINeasy DNA/RNA/Protein All-In-One Kit
Presentations on novel developments in CRISPR screening technologies and applications for the DriverMap™ targeted RNA expression profiling assay