Additional file 2: Table S2. of GAVIN: Gene-Aware Variant INterpretation for medical sequencing
Published in 2017 by
K. van der Velde,
Eddy de Boer,
Cleo van Diemen,
Birgit Sikkema-Raddatz,
Kristin Abbott,
Alain Knopperts,
Lude Franke,
Rolf Sijmons,
Tom de Koning,
Cisca Wijmenga,
Richard Sinke,
Morris Swertz
Abstract
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)