The Most Comprehensive Insight in Cancer Genomes: New Discoveries
The speakers will discuss detecting missing structural variants, characterizing mutation patterns and how nanopore sequencing has advanced their research.
- The capabilities of adaptive sampling, a targeted nanopore sequencing approach
- The importance of structural variant analysis in cancer research
- How a team characterized patterns of mutation occurrences in non-small cell lung cancer genomes
- How methylation and transcriptome data were used to explore possible causes of genomic mutations