GUaRDIAN is a consortium of over 100 clinicians and researchers from over 25 medical and research centers making it one of the largest clinical genomics research networks in India. GUaRDIAN pioneers the clinical application of genomics for Rare Disease Diagnosis and Research.

Ve is a collaborative international effort to systematically collect, analyse and understand the genetic diversity of the Asian populations. We also hope to unravel patterns in genomic diversity modulating phenotypic traits and thus contribute to the baseline data for understanding genomic diversity and healthcare interventions in this area. We hope to make available the entire data and resources available to the larger worldwide scientific community on completion of the project.

In-Vivo Protein Trap Expression in Zebrafish. First Sri Lankan Human Genome. First Malaysian Personal Human Genome. For Potential Interns and Summer Students.

This is the Zv8 version of Wellcome Trust Sanger Institute. Genome Browser for Zebrafish Genomics datasets. A web interface of the WebBLAT program.

Genomics for Personalised and Precision Medicine. Exome Sequence Analysis and Interpretation. Genomics of Rare Genetic Diseases 2015. Exome sequencing reveals a novel mutation, p. L325H, in the KRT5 gene associated with autosomal dominant Epidermolysis Bullosa Simplex Koebner type in a large family from western India. Rare Disease Networks in India. Genome Sequencing to Understand Rare Genetic Disorders.

Vinod Scaria is a m.

Indraprastha Institute of Information Technology, New Delhi. One Day Workshop on Big Data in Genomics. Prof Jalote, director of IIITD signs MOU with Prf. Ghokhale, director of CSIR-IGIB. Human logo for IIITD .