I am a Bioinformatician, with experience in analysis and interpretation of genome level datasets generated from all major High throughput NextGen sequencing (NGS) platforms like ABI SOLiD, 454 GS-FLX, Illumina HiSeq2000, Ion Torrent PGM & MiSeq in a Linux environment. I have worked with NGS data for 3+ years, from optimization of analysis protocols/pipelines, data quality assessment, and biological interpretation of data.
Specialties:Next Gen Sequencing: Hybrid denovo genome assembly, Reference guided assembly(Re-Seq), Whole transcriptome analysis, Targeted sequencing, miRNA prediction, Variant Analysis and Annotation.
NGS Data Analysis Tools: Newbler package, CLCBio Genomics Workbench,...
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