Receive the comprehensive genome analysis you need for your research project. Whole genome sequencing (WGS) provides unprecedented access to genomic information — expediting breakthroughs in healthcare, oncology, biomarker discovery, agriculture, and metagenomics.
GENEWIZ’s expertise in the latest technologies and bioinformatics, including long-read sequencing on the PacBio® Sequel®, enable us to deliver high-quality data and analysis for the genomes of all organisms including humans, animals, plants, bacteria, and viruses.
CLIA-compliant whole genome sequencing (WGS) is also available for clinical researchers.
Assemble novel genomes without a reference sequence
Identify SNVs, short INDELs, and germline/somatic mutations
Discover >50 bp INDELs, translocations, inversions, and copy number variations
Determine which alleles are co-located on the same chromosome
In this PacBio-hosted webinar, Jonas Korlach, PacBio Chief Scientific Officer, and Dave Corney, GENEWIZ Associate Principal Scientist, Next Generation Sequencing, describe the recent release of Sequel System 6.0, which has revolutionized long-read sequencing by providing users the ability to generate highly accurate single-molecule reads.
High-quality high molecular weight (HMW) genomic DNA (≥50 kb) is critical to achieving long read lengths on platforms such as the 10x Genomics® Chromium™ and the PacBio Sequel. Follow these guidelines to generate the best possible WGS results.