We introduce a class of string kernels, called mismatch kernels, for use with support vector machines (SVMs) in a discriminative approach to the protein classification problem. These kernels measure sequence sim- ilarity based on shared occurrences of -length subsequences, counted with up to mismatches, and do not rely on any generative model for the positive training sequences. We compute the kernels efficiently using a mismatch tree data structure and report experiments on a benchmark SCOP dataset, where we show that the mismatch kernel used with an SVM classifier performs as well as the Fisher kernel, the most success- ful method for remote homology detection, while achieving considerable computational savings.

We present a new family of linear time algorithms based on sufficient statistics for string comparison with mismatches under the string kernels framework. Our algorithms improve theoretical complexity bounds of existing approaches while scaling well with respect to the sequence alphabet size, the number of allowed mismatches and the size of the dataset. In particular, on large alphabets with loose mismatch constraints our algorithms are several orders of magnitude faster than the existing algorithms for string comparison under the mismatch similarity measure. We evaluate our algorithms on synthetic data and real applications in music genre classification, protein remote homology detection and protein fold prediction. The scalability of the algorithms allows us to consider complex sequence transformations, modeled using longer string features and larger numbers of mismatches, leading to a state-of-the-art performance with significantly reduced running times.

A key issue in supervised protein classification is the representation of input sequences of amino acids. Recent work using string kernels for protein data has achieved state-of-the-art classification performance. However, such representations are based only on labeled data -- examples with known 3D structures, organized into structural classes -- while in practice, unlabeled data is far more plentiful. In this work, we develop simple and scalable cluster kernel techniques for incorporating unlabeled data into the representation of protein sequences. We show that our methods greatly improve the classification performance of string kernels and outperform standard approaches for using unlabeled data, such as adding close homologs of the positive examples to the training data. We achieve equal or superior performance to previously presented cluster kernel methods while achieving far greater computational efficiency.

A key issue in supervised protein classification is the representation of input sequencesof amino acids. Recent work using string kernels for protein datahas achieved state-of-the-art classification performance. However, suchrepresentations are based only on labeled data -- examples with known 3D structures, organized into structural classes -- while in practice, unlabeled data is far more plentiful. In this work, we develop simpleand scalable cluster kernel techniques for incorporating unlabeled datainto the representation of protein sequences. We show that our methods greatly improve the classification performance of string kernels andoutperform standard approaches for using unlabeled data, such as adding close homologs of the positive examples to the training data. We achieve equal or superior performance to previously presented cluster kernel methods while achieving far greater computational efficiency.

We introduce a class of string kernels, called mismatch kernels, for use with support vector machines (SVMs) in a discriminative approach to the protein classification problem.

We introduce a class of string kernels, called mismatch kernels, for use with support vector machines (SVMs) in a discriminative approach to the protein classification problem.

We introduce a class of string kernels, called mismatch kernels, for use with support vector machines (SVMs) in a discriminative approach to the protein classification problem.