Enhanced Variant Detection and Sample Complexity Representation
Whole genome sequencing (WGS) and RNA sequencing (RNA-Seq) data are increasingly being utilized to analyze functional variants and changes in gene expression. This helps in understanding diseases, including susceptibility and drug response.
Costs have significantly decreased over the past 10 years, but there are still challenges.
Download this poster to find out how to combat these challenges and achieve:
- Visual feedback for higher library prep success.
- Faster workflows.
- Reduced bias in genomic interpretation.
- Clean data revealing transcriptome complexity.
