Abstract
Motivation: RUbioSeq has been developed to facilitate the primary and secondary analysis of re-sequencing projects by providing an integrated software suite of parallelized pipelines to detect exome variants (single-nucleotide variants and copy number variations) and to perform bisulfite-seq analyses automatically. RUbioSeq's variant analysis results have been already validated and published. © The Author 2013.
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CITATION STYLE
Rubio-Camarillo, M., Gómez-López, G., Fernández, J. M., Valencia, A., & Pisano, D. G. (2013). RUbioSeq: A suite of parallelized pipelines to automate exome variation and bisulfite-seq analyses. In Bioinformatics (Vol. 29, pp. 1687–1689). https://doi.org/10.1093/bioinformatics/btt203
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