Whole Exome Sequencing (WES) enables in-depth, targeted interrogation of genomic coding regions while conserving sequencing resources compared to whole genome sequencing (WGS). Rely on Roche Sequencing workflows—from automated DNA extraction through library preparation, exome enrichment, and accurate library quantification—to provide you with high-quality exome results on Illumina ® sequencing platforms.
Deliver superior coverage of recent versions of ACMGv3.1, RefSeq, CCDS, ClinVar, Ensembl, and COSMIC genomic databases. This design also reduces sequencing requirements, with a compact capture target of 43.2 Mb covering 37.5 Mb of key content.
Provides comprehensive coverage and enhanced uniformity with low sequencing requirements. Based on the GRCh38/hg38 human genome assembly, the comprehensive-yet-compact panel efficiently covers content in CCDS, RefSeq, ENSEMBL,and ClinVar.
For Research Use Only. Not for use in diagnostic procedures.
