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We analyse all types of next-generation sequencing data from RNA-seq and single cell RNA-seq to variant sequencing (exome or whole genome), to ChIP-seq or bisulfite sequencing.
We can help you make sense of your results by placing them in biological context through annotation and integration with data sources.
We drive development of bcbio-nextgen, a framework for the automated, scaleable, reproducible analysis of major next-generation sequencing data types.