Next-generation sequencing (NGS) data analysis involves quality control to filter and trim raw sequences, alignment or assembly to map sequences to a reference genome or construct a genome, and variant calling to identify genetic differences, such as mutations or polymorphisms, followed by downstream analysis like annotation and interpretation. Our process encompasses data quality assessment, thorough analysis, result interpretation, and presenting findings to clients in a clear format. It may also involve algorithm development for specific projects. Below is a list of various data analyses offered at Bioinfocloud.