Due to advancement in sequencing technology, it is possible to sequence any or all or selected set of genes in a single shot using Next Generation Sequencing (NGS). These NGS techniques produce sequence in form of short Reads. This page provides facility to align short Reads on selected or all methylation targets. User can visualize and identify any mutation in newly sequenced sample.
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Following is example output file, obtained using this module from paired end Reads using above example file Mate-1 and Mate-2. Mapping of short Reads on drug targets, click for visualization of alignment in Table Viewer