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 â missed,â i.e. not correctly identified as such. From these numbers, we calculated the sensitivity and specificity. (XLSX 58 kb)
Date made available16-Jan-2017
PublisherUniversity of Groningen

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