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and examine SVs are whole genome sequencing reads (or simply reads). The reads mapping over and around variation sites can be used to classify the SV. Previous sequencing technologies often produced
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variability in risk factor susceptibility, treatment response, disease pathogenesis, and clinical diagnosis (biostatistics, machine/deep learning), ii) Investigating causal processes and disease mechanisms
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stratification, discovery of biomarkers for disease risks, diagnosis, drug response and monitoring of health. The precision medicine research is expected to make use of existing strong assets in Sweden and abroad
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