When targeted sequencing won’t do, whole-genome sequencing (WGS) is a fast, unbiased solution for understanding evolutionary relationships and explaining the diversity of any species.
The Rapid Genomics WGS pipeline is automated and optimized to deliver even, consistent, and tunable data across any sample volume. Beyond everyday processes and quality checks, our results are validated against research-jeopardizing index-hopping.
READ MORE ABOUT WGS Read our white paper on index-hopping
Starting from square one? When reference data is not available, WGS can be used alongside RNA-seq data to build custom probe sets for any species using Capture-Seq. We support the full design process from genome and transcriptome assembly, to selection of conserved loci, to full-service sample processing and sequencing.
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