README.md

Introduction

Build Status InBioc

MLSeq is an R/BIOCONDUCTOR package, which provides over 90 algorithms including support vector machines (SVM),random forest (RF), classification and regression trees (CART), Poisson and Negative Binomial Linear Discriminant Analysis (PLDA, NBLDA) and voom-based classifiers (voomDLDA, voomNSC, etc.) for the classification of sequencing data. MLSeq requires a count table as an input which contains the number of reads mapped to each transcript for each sample. This kind of count data can be obtained from RNA-Seq experiments, also from other sequencing experiments such as DNA or ChIP-sequencing. MLSeq includes both normalization (e.g deseq median ratio, trimmed mean of M values) and transformation (variance stabiliation transformation, regularized logarithmic transformation, etc.) techniques which can be performed through classification process. Although the main purpose of MLSeq is to classify samples using a count matrix from RNA-Sequencing data, some of the classifiers which are called sparse classifiers such as PLDA and voomNSC can be used to detect significant features.

To install the MLSeq package in R:

```{r, eval = FALSE, message=FALSE, warning=FALSE} if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager")

BiocManager::install("MLSeq")


If you use MLSeq package in your research, please cite it as below:

> Goksuluk D, Zararsiz G, Korkmaz S, Eldem V, Zararsiz GE, Ozcetin E, Ozturk A, Karaagaoglu AE. MLSeq: Machine
  learning interface for RNA-sequencing data. Computer Methods and Programs in Biomedicine. 2019, 175:223-231.


To get BibTeX entry for LaTeX users, type the following:

```{r, eval = FALSE}
citation("MLSeq")

Please contact us, if you have any questions or suggestions:

gokmenzararsiz@hotmail.com dincer.goksuluk@gmail.com selcukorkmaz@gmail.com

News:

Major changes in version 2.x.y



dncR/MLSeq documentation built on May 17, 2020, 6:45 p.m.