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Part-per-million Variant Detection Service
FromUltima Genomics
Achieve part-per-million SNV detection at low tumor fractions; Enhance rare event detection by leveraging sequencing data from complementary DNA strands to identify and remove false-positive SNV calls generated from sample damage.
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Generate high-quality data from low input DNA samples
Maximize efficiency and sensitivity with the UG 100 Solaris™ workflow, enabling high-quality library prep and data generation. Obtain 30x coverage from 2ng of input from samples like cfDNA on the UG 100 Sequencing Platform.
Simplified library prep with Solaris Free workflow
Use our PCR-free ppmSeq™ Adapters to capture and sequence both strands of the same DNA template without the need for additional UMIs or over-sequencing.