An Introduction to Support Vector Machine Classification

# An Introduction to Support Vector Machine Classification

## An Introduction to Support Vector Machine Classification

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1. An Introduction to Support Vector Machine Classification Bioinformatics Lecture 7/2/2003 by Pierre Dönnes

2. Outline • What do we mean with classification, why is it useful • Machine learning- basic concept • Support Vector Machines (SVM) • Linear SVM – basic terminology and some formulas • Non-linear SVM – the Kernel trick • An example: Predicting protein subcellular location with SVM • Performance measurments

3. Classification • Everyday, all the time we classify things. • Eg crossing the street: • Is there a car coming? • At what speed? • How far is it to the other side? • Classification: Safe to walk or not!!!

4. Outlook Sunny Overcast Rain Yes Humidity Wind Normal Strong Weak High No Yes No Yes • Decision tree learning • IF (Outlook = Sunny) ^ (Humidity = High) • THENPlayTennis =NO • IF (Outlook = Sunny)^ (Humidity = Normal) • THEN PlayTennis = YES • Training examples: • Day Outlook Temp. Humidity Wind PlayTennis • D1 Sunny Hot High Weak No • D2 Overcast Hot High Strong Yes ……

5. Classification tasks in Bioinformatics • Learning Task • Given: Expression profiles of leukemia patients and healthy persons. • Compute: A model distinguishing if a person has leukemia from expression data. • Classification Task • Given: Expression profile of a new patient + a learned model • Determine: If a patient has leukemia or not.

6. Problems in classifying biological data • Often high dimension of data. • Hard to put up simple rules. • Amount of data. • Need automated ways to deal with the data. • Use computers – data processing, statistical analysis, try to learn patterns from the data (Machine Learning)

7. Examples are: - Support Vector Machines - Artificial Neural Networks - Boosting - Hidden Markov Models

8. Test-data Prediction = cancer or not Black box view ofMachine Learning Training data Model Model Magic black box (learning machine) Training data: -Expression patterns of some cancer + expression data from healty person Model: - The model can distinguish between healty and sick persons. Can be used for prediction.

9. Tennis example 2 Temperature Humidity = play tennis = do not play tennis

10. Linear Support Vector Machines Data: <xi,yi>, i=1,..,l xi  Rd yi  {-1,+1} x2 =+1 =-1 x1

11. =-1 =+1 Linear SVM 2 Data: <xi,yi>, i=1,..,l xi  Rd yi  {-1,+1} f(x) All hyperplanes in Rd are parameterize by a vector (w) and a constant b. Can be expressed as w•x+b=0 (remember the equation for a hyperplane from algebra!) Our aim is to find such a hyperplane f(x)=sign(w•x+b), that correctly classify our data.

12. d+ d- Definitions Define the hyperplane H such that: xi•w+b  +1 when yi =+1 xi•w+b  -1 when yi =-1 H1 H2 H1 and H2 are the planes: H1: xi•w+b = +1 H2: xi•w+b = -1 The points on the planes H1 and H2 are the Support Vectors H d+ = the shortest distance to the closest poitive point d- = the shortest distance to the closest negative point The margin of a separating hyperplane is d+ + d-.

13. d+ d- Maximizing the margin We want a classifier with as big margin as possible. H1 H H2 Recall the distance from a point(x0,y0) to a line: Ax+By+c = 0 is|A x0 +B y0 +c|/sqrt(A2+B2) The distance between H and H1 is: |w•x+b|/||w||=1/||w|| The distance between H1 and H2 is: 2/||w|| In order to maximize the margin, we need to minimize ||w||. With the condition that there are no datapoints between H1 and H2: xi•w+b  +1 when yi =+1 xi•w+b  -1 when yi =-1 Can be combined into yi(xi•w)  1

14. The Lagrangian trick Reformulate the optimization problem: A ”trick” often used in optimization is to do an Lagrangian formulation of the problem.The constraints will be replace by constraints on the Lagrangian multipliers and the training data will only occur as dot products. Gives us the task: Max Ld = i – ½ijxi•xj, Subject to: w = iyixi iyi = 0 What we need to see: xiand xj (input vectors) appear only in the form of dot product – we will soon see why that is important.

15. Problems with linear SVM =-1 =+1 What if the decison function is not a linear?

16. Remember the function we want to optimize: Ld = i – ½ijxi•xj, xi and xj as a dot product. We will have (xi) • (xj) in the non-linear case. If there is a ”kernel function” K such as K(xi,xj) = (xi) • (xj), we do not need to know  explicitly. One example: Non-linear SVM 1 The Kernel trick Imagine a function  that maps the data into another space: =Rd Rd  =-1 =+1  =-1 =+1

17. Non-linear svm2 The function we end up optimizing is: Max Ld = i – ½ijK(xi•xj), Subject to: w = iyixi iyi = 0 Another kernel example: The polynomial kernel K(xi,xj) = (xi•xj + 1)p, where p is a tunable parameter. Evaluating K only require one addition and one exponentiation more than the original dot product.

18. Solving the optimization problem • In many cases any general purpose optimization package that solves linearly constrained equations will do. • Newtons’ method • Conjugate gradient descent • Other methods involves nonlinear programming techniques.

19. =-1 =+1 Overtraining/overfitting A well known problem with machine learning methods is overtraining. This means that we have learned the training data very well, but we can not classify unseen examples correctly. An example: A botanist really knowing trees.Everytime he sees a new tree, he claims it is not a tree.

20. Overtraining/overfitting 2 A measure of the risk of overtraining with SVM (there are also other measures). It can be shown that: The portion, n, of unseen data that will be missclassified is bound by: n  No of support vectors / number of training examples Ockham´s razor principle: Simpler system are better than more complex ones. In SVM case: fewer support vectors mean a simpler representation of the hyperplane. Example: Understanding a certain cancer if it can be described by one gene is easier than if we have to describe it with 5000.

21. A practical example, protein localization • Proteins are synthesized in the cytosol. • Transported into different subcellular locations where they carry out their functions. • Aim: To predict in what location a certain protein will end up!!!

22. Subcellular Locations

23. Method • Hypothesis: The amino acid composition of proteins from different compartments should differ. • Extract proteins with know subcellular location from SWISSPROT. • Calculate the amino acid composition of the proteins. • Try to differentiate between: cytosol, extracellular, mitochondria and nuclear by using SVM

24. Input encoding Prediction of nuclear proteins: Label the known nuclear proteins as +1 and all others as –1. The input vector xi represents the amino acid composition. Eg xi =(4.2,6.7,12,….,0.5) A , C , D,….., Y) Nuclear SVM Model All others

25. Cross-validation Cross validation: Split the data into n sets, train on n-1 set, test on the set left out of training. 1 Test set Nuclear 1 1 2 3 2 1 All others Training set 3 2 2 3 3

26. SP = TP /(TP+FP), the fraction of predicted +1 that actually are +1. SE = TP /(TP+FN), the fraction of the +1 that actually are predicted as +1. In this case: SP=5/(5+1) =0.83 SE = 5/(5+2) = 0.71 Performance measurments TP Test data Predictions FP Model +1 TN -1 =+1 =-1 FN

27. Results • We definetely get some predictive power out of our models. • Seems to be a difference in composition of proteins from different subcellular locations. • Another questions: What about nuclear proteins. Is there a difference between DNA-binding proteins and others???

28. Conclusions • We have (hopefully) learned some basic concepts and terminology of SVM. • We know about the risk of overtraining and how to put a measure on the risk of bad generalization. • SVMs can be useful for example in predicting subcellular location of proteins.

29. You can’t input anything into a learning machine!!! Image classification of tanks. Autofire when an enemy tank is spotted. Input data: Photos of own and enemy tanks. Worked really good with the training set used. In reality it failed completely. Reason: All enemy tank photos taken in the morning. All own tanks in dawn. The classifier could recognize dusk from dawn!!!!

30. AN INTRODUCTION TO SUPPORT VECTOR MACHINES(and other kernel-based learning methods)N. Cristianini and J. Shawe-TaylorCambridge University Press2000 ISBN: 0 521 78019 5 References http://www.kernel-machines.org/ http://www.support-vector.net/ Papers by Vapnik C.J.C. Burges: A tutorial on Support Vector Machines. Data Mining and Knowledge Discovery 2:121-167, 1998.