Can Whole Genome Sequencing Identify All Types of Cancer Mutations?
Yes, WGS can identify a wide range of mutations, including those in non-coding regions of the genome which are often missed by other sequencing methods. This includes SNPs, insertions, deletions, copy number variations, and structural variants. However, it is essential to pair WGS data with other analyses, such as transcriptomics and proteomics, to get a complete picture.
