methylKit: User Guide vr packageVersion('methylKit')
Introduction | DNA methylation | High-throughput bisulfite sequencing | Basics | Reading the methylation call files | Reading the methylation call files and store them as flat file database | Reading the methylation calls from sorted Bismark alignments | Descriptive statistics on samples | Filtering samples based on read coverage | Comparative analysis | Merging samples | Sample Correlation | Clustering samples | Batch effects | Tiling windows analysis | Finding differentially methylated bases or regions | Correcting for overdispersion | Accounting for covariates | Finding differentially methylated bases using multiple-cores | Annotating differentially methylated bases or regions | Regional analysis | Convenience functions for annotation objects | methylKit convenience functions | Coercing methylKit objects to GRanges | Converting methylKit objects to methylDB objects and vice versa | Loading methylDB objects from tabix files | Selection: subsetting methylKit Objects | selectByOverlap | reorganize(): reorganizing samples and treatment vector within methylKit objects | percMethylation(): Getting percent methylation matrix from methylBase objects | methSeg(): segmentation of methylation or differential methylation profiles | Frequently Asked Questions | How can I select certain regions/bases from methylRaw or methylBase objects ? | How can I find if my regions of interest overlap with | How can I find the nearest TSS associated with my CpGs ? | How do you define promoters and CpG island shores ? | What does Bismark SAM output look like, where can I get more info ? | How can I reorder or remove samples at/from methylRawList or methylBase | Should I normalize my data ? | How can I force methylKit to use Fisher's exact test ? | Can use data from other aligners than Bismark in methylKit ? | Can I transform an methylKit object into an methylDB object ? | How could I share methylKit objects ? | Where do I find the flatfile database underlying a methylDB? | Why does my methylBaseDB flatfile database has a different name now ? | How can I make a bigwig file from methylKit result? | My data comes from MIRA-seq, can I use methylKit to perform the differential | My data comes from Methylation arrays, can I use methylKit to analyse my data ? | How can I analyze data generated from a local alignment ? | How can I analyze data generated from a spliced alignment ? | Why does the regionCount function not keep the input region order? | How can I merge muliple separate methylRaw objects into a methylRawList? | Acknowledgements | Full list of contributors | R session info | References