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Analysis of Sequence Data

We provide, almost complete analysis of NGS data for genomics research, including WGS, (targeted) exome sequencing, Methyl-Seq, also beyond genomics e.g. RNA-Seq and ChIP-Seq. We provide support not only for the analysis of the resulting data, but also actually in designing your experiment for getting maximum information from your experiment. We empower your work, by de-noising your raw data, (de novo) assembly, mapping, alignment (e.g. BLAST), annotation, SNP calling, variant analysis and finally (differential) expression analysis.