Article

Annotations of Recurrent Structural Variant Events in Pan-cancer Whole Genome Data for Precision Medicine

2021-01-04

Abstract excerpt

In personalized cancer genomic medicine, characterizing a patient’s molecular profile based on comprehensive information is important for maximizing treatment benefits. However, current cancer genome analysis is centered on single nucleotide variation (SNV), gene expression, and copy number variation (CNV) but places little emphasis on structural variations (SV) beside fusions. To date, investigation of SVs has be...

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Literature Corpus work: b85d6b34-5747-5b7a-a6a7-f8d4f530c0f6
DOI: 10.21203/rs.3.rs-136297/v1

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