Abstract
Computational genomics seeks to draw biological infer- ences from genomic datasets, often by integrating and contextualiz- ing next generation sequencing (NGS) data. CGAT provides an extensive suite of tools designed to assist in the analysis of genome scale data from a range of standard file formats. The toolkit enables filtering, comparison, conversion, summarization and annotation of genomic intervals, genesets and sequences. The tools can both be run from the Unix command line and installed into visual workflow builders, such as Galaxy.
Cite
CITATION STYLE
Lange, J. (2010). Tag der offenen Tür. MMW - Fortschritte Der Medizin, 152(12), 17–17. https://doi.org/10.1007/bf03366256
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