Screening For Rare Genetic Disorders At a Point-Of-Click

Genomics_2927230fFast and accurate diagnosis of disease-causing mitochondrial genetic mutations is now possible thanks to automation of the entire process of data analysis and interpretation by a team of researchers at the Delhi-based CSIR Institute of Genomics and Integrative Biology.

The comprehensive pipeline developed by a team led by Dr. Sridhr

Sivasubbu and Dr. Vinod Scaria of IGIB includes methodologies to sequence mitochondrial genome using next generation sequencing and a software to appropriately analyse and interpret the data at a point-of-click.

Click here to read more.

Upcoming Events
From 29-February-2020
to 21-June-2020

RaceFor7USA 2020

1) Washington DC
2) SF Bay area, CA
3) Greenville, SC
4) Boston (Acton), MA
5) Frisco, TX

Subscribe to our ORDI USA Newsletter:

Highslide for Wordpress Plugin