Structural Variation identification in Breast Cancer with Whole Genome Sequencing using...
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...