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