Whole genome sequencing (WGS) provides a high-resolution, base-by-base view of the entire genome, which is essential for understanding genetic variations and their implications in health and disease. Since there’s no need to pre-select genomic regions to examine, WGS is a powerful tool for variant discovery and helps inform your next set of research questions.
Whole genome sequencing leverages high-throughput sequencing technology to generate comprehensive genomic data, providing insights into genetic variations and their functional implications.
This powerful, cutting-edge technology allows for the rapid and accurate sequencing of entire genomes, facilitating large-scale genomic studies and discovery of new research targets in the oncology and rare disease areas. Leave no genomic question unanswered. Support your research with reliable and high-quality data by interrogating widely or targeting specific biomarkers.
Contact us to learn more about our WGS solutions and how they can support your research. Our team of experts is ready to assist you in selecting the right products and services.
Efficient and accurate library preparation for whole genome sequencing
Adapters and primers available for Illumina®, Ultima Genomics®, Element, and DNBSEQ™ sequencing platforms
Tool to guide you through the design of custom adapters
High library complexity from low quality samples
Ensures that each library is equally represented, and saves you having to manually adjust
Tools to help reduce barriers and enable you to achieve your research goals
Whole genome sequencing provides comprehensive coverage over the entire mappable genome to gain information about an organism or metagenomic DNA samples. After sequencing, the individual sequenced fragments of the genome are aligned to a reference genome for variant analysis, assembled into contigs for de novo genome assemblies, or used for microbial classification (in the case of metagenomic samples).
