The most powerful approach to scan for unspecific germline variations, somatic mutations, and structural variants is high-throughput sequencing. Whole-genome sequencing, exome sequencing, and targeted region sequencing are three of the most common sequencing concepts in DNA sequencing. While highly useful, in different aspects of data collection, computation time, and variant detection precision, sequencing data creates […]
CD Genomics Blog
Explore the blog we’ve developed, including genomic education, genomic technologies, genomic advances, and genomics news & views.