Structural Variation identification in Breast Cancer with Whole Genome Sequencing using Long reads
doi: https://doi.org/10.1101/847855 Link: https://www.biorxiv.org/content/biorxiv/early/2019/11/19/847855.full.pdf Advancement of high throughput sequencing technologies have enabled researchers to identify or screen cancer causing structural variants. Long-read, single molecule sequencing technologies from Pacific Biosciences (PacBio) and Oxford Nanopore Technologies (ONT) have been shown as most reliable…