How to evaluate performance of prediction methods? Measures and their interpretation in variation effect analysis

被引:190
作者
Vihinen, Mauno [1 ,2 ,3 ]
机构
[1] Univ Tampere, Inst Biomed Technol, FI-33014 Tampere, Finland
[2] BioMediTech, Tampere, Finland
[3] Lund Univ, Dept Expt Med Sci, SE-22184 Lund, Sweden
来源
BMC GENOMICS | 2012年 / 13卷
关键词
MULTIPLE SEQUENCE ALIGNMENT; PROTEIN STABILITY; BENCHMARK; CLASSIFICATION; MUTATIONS; ACCURACY; DATABASES;
D O I
10.1186/1471-2164-13-S4-S2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Prediction methods are increasingly used in biosciences to forecast diverse features and characteristics. Binary two-state classifiers are the most common applications. They are usually based on machine learning approaches. For the end user it is often problematic to evaluate the true performance and applicability of computational tools as some knowledge about computer science and statistics would be needed. Results: Instructions are given on how to interpret and compare method evaluation results. For systematic method performance analysis is needed established benchmark datasets which contain cases with known outcome, and suitable evaluation measures. The criteria for benchmark datasets are discussed along with their implementation in VariBench, benchmark database for variations. There is no single measure that alone could describe all the aspects of method performance. Predictions of genetic variation effects on DNA, RNA and protein level are important as information about variants can be produced much faster than their disease relevance can be experimentally verified. Therefore numerous prediction tools have been developed, however, systematic analyses of their performance and comparison have just started to emerge. Conclusions: The end users of prediction tools should be able to understand how evaluation is done and how to interpret the results. Six main performance evaluation measures are introduced. These include sensitivity, specificity, positive predictive value, negative predictive value, accuracy and Matthews correlation coefficient. Together with receiver operating characteristics (ROC) analysis they provide a good picture about the performance of methods and allow their objective and quantitative comparison. A checklist of items to look at is provided. Comparisons of methods for missense variant tolerance, protein stability changes due to amino acid substitutions, and effects of variations on mRNA splicing are presented.
引用
收藏
页数:10
相关论文
共 35 条
[1]   Issues in bioinformatics benchmarking: the case study of multiple sequence alignment [J].
Aniba, Mohamed Radhouene ;
Poch, Olivier ;
Thompson, Julie D. .
NUCLEIC ACIDS RESEARCH, 2010, 38 (21) :7353-7363
[2]   Assessing the accuracy of prediction algorithms for classification: an overview [J].
Baldi, P ;
Brunak, S ;
Chauvin, Y ;
Andersen, CAF ;
Nielsen, H .
BIOINFORMATICS, 2000, 16 (05) :412-424
[3]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[4]   A benchmark for affymetrix GeneChip expression measures [J].
Cope, LM ;
Irizarry, RA ;
Jaffee, HA ;
Wu, ZJ ;
Speed, TP .
BIOINFORMATICS, 2004, 20 (03) :323-331
[5]   Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project [J].
Cotton, Richard G. H. ;
Al Aqeel, Aida I. ;
Al-Mulla, Fahd ;
Carrera, Paola ;
Claustres, Mireille ;
Ekong, Rosemary ;
Hyland, Valentine J. ;
Macrae, Finlay A. ;
Marafie, Makia J. ;
Paalman, Mark H. ;
Patrinos, George P. ;
Qi, Ming ;
Ramesar, Rajkumar S. ;
Scott, Rodney J. ;
Sijmons, Rolf H. ;
Sobrido, Maria-Jesus ;
Vihinen, Mauno .
GENETICS IN MEDICINE, 2009, 11 (12) :843-849
[6]  
Desmet F, 2010, RES ADV NUCL ACID RE
[7]   MUSCLE: multiple sequence alignment with high accuracy and high throughput [J].
Edgar, RC .
NUCLEIC ACIDS RESEARCH, 2004, 32 (05) :1792-1797
[8]   An introduction to ROC analysis [J].
Fawcett, Tom .
PATTERN RECOGNITION LETTERS, 2006, 27 (08) :861-874
[9]   PhenCode:: Connecting ENCODE data with mutations and phenotype [J].
Giardine, Belinda ;
Riemer, Cathy ;
Hefferon, Tim ;
Thomas, Daryl ;
Hsu, Fan ;
Zielenski, Julian ;
Sang, Yunhua ;
Elnitski, Laura ;
Cutting, Garry ;
Trumbower, Heather ;
Kern, Andrew ;
Kuhn, Robert ;
Patrinos, George P. ;
Hughes, Jim ;
Higgs, Doug ;
Chui, David ;
Scriver, Charles ;
Phommarinh, Manyphong ;
Patnaik, Santosh K. ;
Blumenfeld, Olga ;
Gottlieb, Bruce ;
Vihinen, Mauno ;
Valiaho, Jouni ;
Kent, Jim ;
Miller, Webb ;
Hardison, Ross C. .
HUMAN MUTATION, 2007, 28 (06) :554-562
[10]  
Gray J., 1993, The Benchmark Handbook for Database and Transaction Systems, Vsecond