Vinod Scaria
http://dbpedia.org/resource/Vinod_Scaria an entity of type: Thing
Dr. Vinod Scaria FRSB, FRSPH (born 9 March 1981) is an Indian biologist, medical researcher pioneering in Precision Medicine and Clinical Genomics in India. He is best known for sequencing the first Indian genome. He was also instrumental in the sequencing of The first Sri Lankan Genome, analysis of the first Malaysian Genome sequencing and analysis of the Wild-type strain of Zebrafish and the IndiGen programme on Genomics for Public Health in India
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Vinod Scaria
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Dr. Vinod Scaria
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Dr. Vinod Scaria
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Mbinga, Tanzania
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1981-03-09
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38480455
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1105915612
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Indraprastha Institute of Information Technology Delhi,
Institute of Genomics and Integrative Biology, Academy of Scientific and Innovative Research
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FRSB
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CSIR Young Scientist Award
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1981-03-09
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Dr. Vinod Scaria
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Indian
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Indian
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Delhi, India
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Dr. Vinod Scaria FRSB, FRSPH (born 9 March 1981) is an Indian biologist, medical researcher pioneering in Precision Medicine and Clinical Genomics in India. He is best known for sequencing the first Indian genome. He was also instrumental in the sequencing of The first Sri Lankan Genome, analysis of the first Malaysian Genome sequencing and analysis of the Wild-type strain of Zebrafish and the IndiGen programme on Genomics for Public Health in India He is presently a scientist at CSIR Institute of Genomics and Integrative Biology and an adjunct faculty at Indraprastha Institute of Information Technology, Delhi. He along with his colleague and collaborator Sridhar Sivasuubu are widely regarded as the pioneers in the area of clinical genomics in India. They are also the co-founders of the Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN) a large clinical network working in the area of Rare Disease Genomics in India. They were also instrumental in setting up a comprehensive fellowship programme in genomics for clinicians His research has also contributed to a number of commercially viable technologies for healthcare and public health applications. This includes one of the methods for fast and accurate diagnosis and screening of mitochondrial genetic diseases.
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32934