| 摘要 |
The present invention relates to a method and a system for detecting a cancer-related major genetic variation from genetic data of cancer patients and, more specifically, relates to a method for detecting a cancer-related major generic variation, which comprises: a sequence data collection step of collecting a plurality of sequence data which are formed into data by extracting genetic materials from a plurality of cancer patients; a backbone data generation step of determining each genetic variation by location of the sequence data, and generating a backbone data sheet for the entire sequence data by merging determination results of the genetic variation by location of the sequence data; a cancer-related genetic variation analysis step of generating cancer-related genetic variation location information data for each of the sequence data by analyzing relevance to cancer by the location of the genetic variation for each of the sequence data; and an integrated cancer-related genetic variation data generation step of generating integrated cancer-related data for the entire sequence data by mapping each of the cancer-related genetic variation location information data on the backbone data sheet. According to the present invention, the method can reduce time and costs required for obtaining information of the cancer-related genetic variation and more accurately and reliably analyze the cancer-related genetic variation. |
