Developing analysis pipeline for whole genome sequencing data (raw data QC, mapping, marking duplicate, coverage etc.); Developing mutation calling and annotation pipeline; Analyzing next-generation sequencing data using popular NGS analysis tools like BWA, GATK, Samtools etc.; Analyzing next-generation sequencing data using the publicly available biological databases and servers like NCBI, KEGG, GeneBank, Pfam etc.; Development of bioinformatics tools for RNA secondary structure analysis etc.