Additional file 2: Table S2. of GAVIN: Gene-Aware Variant INterpretation for medical sequencing

Detailed overview of all benchmark results. Each combination of tool and dataset is listed. We provide the raw counts of true positives (TP), true negatives (TN), false positives (FP), and false negatives (FN), as well as of pathogenic and benign variants that were “missed,” i.e. not correctly identified as such. From these numbers, we calculated the sensitivity and specificity. (XLSX 58 kb)

所有基准测试结果的详细概览。本数据集列出了工具与数据集的全部组合。我们提供了真阳性（TP）、真阴性（TN）、假阳性（FP）与假阴性（FN）的原始计数，以及被「漏检」（即未被正确识别为致病或良性）的致病与良性变异的原始计数。基于上述数值，我们计算了灵敏度与特异度。(XLSX 58 kb)