SignS: a parallelized, open-source, freely available, web-based tool for gene selection and molecular signatures for survival and censored data

We have developed SignS (Signatures for Survival data), an open-source, freely-available, web-based tool and R package for gene selection, building molecular signatures, and prediction with survival data. SignS implements four methods which, according to existing reviews, perform well and, by being of a very different nature, offer complementary approaches. We use parallel computing via MPI, leading to large decreases in user waiting time. Cross-validation is used to asses predictive performance and stability of solutions, the latter an issue of increasing concern given that there are often several solutions with similar predictive performance. Biological interpretation of results is enhanced because genes and signatures in models can be sent to other freely-available on-line tools for examination of PubMed references, GO terms, and KEGG and Reactome pathways of selected genes.SignS is the first web-based tool for survival analysis of expression data, and one of the very few with biomedical researchers as target users. SignS is also one of the few bioinformatics web-based applications to extensively use parallelization, including fault tolerance and crash recovery. Because of its combination of methods implemented, usage of parallel computing, code availability, and links to additional data bases, SignS is a unique tool, and will be of immediate relevance to biomedical researchers, biostatisticians and bioinformaticians.Many microarray studies involve human samples for which survival data are available. In the last two years there has been an increase in the number of new methods proposed for this kind of data [1-11]. Many of these papers have emphasized not only gene selection and survival prediction, but also "signature finding": discovering sets of correlated genes that are relevant for survival prediction. For end-users (e.g., biomedical researchers with microarray data for a sample of patients for which survival is known), however, most of these methods are not