Collaborative project


    Whole exome sequencing data analysis in UPD14-like diseases

    In collaboration with Dr Kagami, Dr Sekita and Dr Mizuguchi, we are trying to find the cause of a severe group of congenital diseases which show the same symptoms as Uni-parental disomy. Currently, the whose exome sequencing of several patients has been completed and a disease signature is being established.

    Collaborative project completed

    Philip Prathipati (NIBIOHN, Japan) has published a paper on

    accurate pose prediction,

    in protein-ligand docking

    in which I contributed in

    data analysis and discussions.

    Read the paper here

    © Prof Shandar Ahmad Research Group. | Developed by Sudhir Patwal