What R packages and their functions can perform variant calling on .sam and .bam files? Need a commented clear code example. Found RSamtools. No concrete examples in their documentation therein.
What R packages and their functions can perform variant calling on .sam and .bam files? Need a commented clear code example. Found RSamtools. No concrete examples in their documentation therein.
I'm pretty sure you went under the other account name "vassialk"... Any reason why you're mass posting to this site without clarification? Are you a bot? - In reference to your question, I don't think RSamtools implements the variant calling aspects of the package in R. You're better off using a bash based approach to doing variant calling. There are no R packages for running a full variant calling analysis as far as I'm aware.
There is VariantTools in Bioconductor, and here are some introductory slides. (Haven't used it so far.) There are more useful packages in BioC View GenomicVariation.
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