Hi, 

I am currently working on next generation sequencing platform. I will be pleased to hear if someone in the group could help me get into variant call methods (particularly SNPeff, SAMtools and bcftools platform). 

Thank you 

​

Sanjay Gautam, B.Sc. MLT, M.Sc. Med. Microbiology

PhD Student/School of Medicine/ Breathe Well Center

University of Tasmania, 17 Liverpool Street, Hobart TAS 7000,Australia

M +61416181795 / E.mail: Sanjay.Gautam@utas.edu.au

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