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Genomics for Precision Medicine India

Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN). 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. Omics for Precise Therapeutic Interventions Minimizing Adverse Events (OPTIMA). Our work In News. Jacob Koshy in the Hindu (1st Jan 2017).

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Genomics for Precision Medicine India | meragenome.com Reviews
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Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN). 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. Omics for Precise Therapeutic Interventions Minimizing Adverse Events (OPTIMA). Our work In News. Jacob Koshy in the Hindu (1st Jan 2017).
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Genomics for Precision Medicine India | meragenome.com Reviews

https://meragenome.com

Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN). 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. Omics for Precise Therapeutic Interventions Minimizing Adverse Events (OPTIMA). Our work In News. Jacob Koshy in the Hindu (1st Jan 2017).

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Rare Disease Genomics India - GUaRDIAN | Genomics for Understanding Rare Diseases - India Alliance Network

Patient Support and Education. Clinical Genomics Meeting (ClinGeM). Genomics for Personalised and Precision Medicine. Exome Sequence Analysis and Interpretation. Genomics of Rare Genetic Diseases 2015. Patient Support and Education. 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.

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Indian Genome - meragenome.com | personal genomics for everyone

http://www.meragenome.com/indian-genome

The Indian Genome Announcement. The first Indian Genome was announced on 8th of December 2009. To this effect, an announcement was made in the Lok Sabha by Shri Prithviraj Chavan, Minister of State (Independent Charge) of Science and Technology on Sequencing of the first human genome in India. Shri Prithviraj Chavan, Minister of State (Independent Charge) of Science and Technology with the CSIR. Team on announcing of the sequencing of the first human genome in India. 2012) Accepted [ Genome Browser.

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News Updates - meragenome.com | personal genomics for everyone

http://www.meragenome.com/news-updates-1

Posted Jun 10, 2012, 3:11 AM. By admin admin@meragenome.com. We have the first website preview today. We hope to go online after a few content additions and proof reading. We are actively working on the back-end as well as the publicity material for the release. Posted May 16, 2012, 9:41 PM. By admin admin@meragenome.com [ updated May 17, 2012, 3:40 AM. We have just unveiled the meragenome.com logo. The logo depicts " kundali. An ancient Indian horoscope. Meragenome.com goes online.

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Benefits - meragenome.com | personal genomics for everyone

http://www.meragenome.com/personal-genomics/benefits

Benefits of Personal Genome Sequencing. The present state of the art of genome analysis provides individuals with a number of recommendations regarding genetic predispositions and drug response which could potentially improve clinical decision-making, or positively impact personal health. It could also potentially provide for recommendations for diagnostic tests or medical consultation. Personalised Drugs and Treatment. It should also be emphasized that the present state of art is still not in any shape ...

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How it works - meragenome.com | personal genomics for everyone

http://www.meragenome.com/how-it-works

For the first time in the history of Human civilisation, the technology enables Inexpensive, time-efficient full genome sequencing. This advances in technology now enables individuals to be able to have their entire genome sequenced. Extensive analysis of this information is suggested to have far-reaching impact on personalized heathcare, enabling physicians to prescribe the optial treatment based on your geentic makeup. As more knowledge and understanding is being generated on an exponential pace on gen...

5

Caveats - meragenome.com | personal genomics for everyone

http://www.meragenome.com/caveats

Personal genome sequencing are not without caveats. Primarily there have been no conclusively proven evidence suggesting personal genome sequencing could provide healthcare benefits to individuals, though can provide you with clues towards improving your lifestyle. Except for Mendelian diseases, majority of markers provide minimal risk, many of the risks are not significantly clinically actionable. Infer paternity and infer ancestry and genealogy. Claim or incriminate you or your close relatives in crime.

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Open Source Drug Discovery: May 2008

http://opensourcedrugdiscovery.blogspot.com/2008_05_01_archive.html

Open Source Drug Discovery. Saturday, May 3, 2008. Financial Express runs a commentary on the Indian Initiative for Open Source Drug Discovery for neglected diseases. To work together in discovering new drugs for diseases like tuberculosis (TB), malaria, various types of cancer, AIDS, Chikungunya, Kala-azar, dengue fever, etc. Not only would drugs be made available to the public at affordable prices, there are monetary gains for the participating researchers in the form of awards and prizes. The full-tex...

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News - Vinod Scaria MBBS, PhD

http://vinodscaria.rnabiology.org/news

Open Source Drug Discovery. Screening for rare genetic disorders at a point-of-click. (The Hindu July 10, 2016). Posted Jul 12, 2016, 3:05 AM. By Vinod Scaria [ updated Jul 12, 2016, 3:09 AM. Full-text http:/ www.thehindu.com/sci-tech/health/screening-for-rare-genetic-disorders-at-a-pointofclick/article8831110.ece. Should you take that genetic test? Jacob Koshy (The Hindu May 15, 2016). Posted Jun 28, 2016, 2:48 AM. By Vinod Scaria [ updated Jun 28, 2016, 2:48 AM. Posted Jun 14, 2016, 9:32 PM. Scientists...

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Science and Society - Vinod Scaria MBBS, PhD

http://vinodscaria.rnabiology.org/science-and-society

Open Source Drug Discovery. In collaboration with Sridhar Sivasubbu Lab). We work closely with Patients, Patient Support Groups and Clinicians towards popularizing genomics and its applications in clinical settings. Clinical Collaboration- Genomics of Rare Genetic Diseases-. Read more on our initiative to understand rare genetic diseases in India using genomics tools involving a large number of clinicians and researchers. ( Visit GUaRDIAN Website. Vellarikkal et al (2015) Human Mutation. In collaboration...

opensourcedrugdiscovery.blogspot.com opensourcedrugdiscovery.blogspot.com

Open Source Drug Discovery: Treatment Outcomes and Survival Based on Drug Resistance Patterns in Multidrug-resistant Tuberculosis.

http://opensourcedrugdiscovery.blogspot.com/2010/03/treatment-outcomes-and-survival-based.html

Open Source Drug Discovery. Monday, March 15, 2010. Treatment Outcomes and Survival Based on Drug Resistance Patterns in Multidrug-resistant Tuberculosis. Treatment Outcomes and Survival Based on Drug Resistance Patterns in Multidrug-resistant Tuberculosis. Am J Respir Crit Care Med. 2010 Mar 11;. Kim DH, Kim HJ, Park SK, Kong SJ, Kim YS, Kim TH, Kim EK, Lee KM, Lee SS, Park JS, Koh WJ, Lee CH, Shim TS". Subscribe to: Post Comments (Atom). Open Source Drug Discovery Links. OSDD Group on Google Groups.

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Open Source Drug Discovery: November 2010

http://opensourcedrugdiscovery.blogspot.com/2010_11_01_archive.html

Open Source Drug Discovery. Sunday, November 28, 2010. OSDD JSF and WSF. JOINT MEETING cum WORKSHOP. OSDD - WSF and OSDD - JSF. Farook College and Devakiamma College of Pharmacy. 1 As part of the one day workshop organized in the two colleges one team comprising of Dr U.C.A. Jaleel, Harish (Research Scholar, MCC), Hari (Zamorins Guruvayurappan College) and Shamshudeen osdd cheminformatics went to the Devakiamma College to conduct the Morning Session. 5 The second session also was spiced up by the skype m...

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Open Source Drug Discovery: India Takes an Open Source Approach to Drug Discovery

http://opensourcedrugdiscovery.blogspot.com/2008/05/india-takes-open-source-approach-to.html

Open Source Drug Discovery. Saturday, May 3, 2008. India Takes an Open Source Approach to Drug Discovery. India Takes an Open Source Approach to Drug Discovery. Cell, Vol 133, 201-203, 18 April 2008. Cell Press covers the Indian Initiative on Open Source Drug Discovery in an Analysis article authored by Seema Singh. The article in short summarizes the concept of Open Source Drug Discovery for neglected diseases, especially Tuberculosis. Comment on this article. On Cell Press website.

opensourcedrugdiscovery.blogspot.com opensourcedrugdiscovery.blogspot.com

Open Source Drug Discovery: OSDD JSF and WSF

http://opensourcedrugdiscovery.blogspot.com/2010/11/fwd-osdd-wsf-and-jsf.html

Open Source Drug Discovery. Sunday, November 28, 2010. OSDD JSF and WSF. JOINT MEETING cum WORKSHOP. OSDD - WSF and OSDD - JSF. Farook College and Devakiamma College of Pharmacy. 1 As part of the one day workshop organized in the two colleges one team comprising of Dr U.C.A. Jaleel, Harish (Research Scholar, MCC), Hari (Zamorins Guruvayurappan College) and Shamshudeen osdd cheminformatics went to the Devakiamma College to conduct the Morning Session. 5 The second session also was spiced up by the skype m...

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Genomics for Precision Medicine India

Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN). 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. Omics for Precise Therapeutic Interventions Minimizing Adverse Events (OPTIMA). Our work In News. Jacob Koshy in the Hindu (1st Jan 2017).

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