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

Genomics for Rare DIseases in India Genomics for Understanding Rare Diseases - India Alliance Network. Personal Genomics in India | Indian Genome | Rare Disease India | Genetic Diseases India | Mendelian Disorders India | Genomics India

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Rare Disease Genomics India - GUaRDIAN | Genomics for Understanding Rare Diseases - India Alliance Network | guardian.meragenome.com Reviews
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Genomics for Rare DIseases in India Genomics for Understanding Rare Diseases - India Alliance Network. Personal Genomics in India | Indian Genome | Rare Disease India | Genetic Diseases India | Mendelian Disorders India | Genomics India
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Rare Disease Genomics India - GUaRDIAN | Genomics for Understanding Rare Diseases - India Alliance Network | guardian.meragenome.com Reviews

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Genomics for Rare DIseases in India Genomics for Understanding Rare Diseases - India Alliance Network. Personal Genomics in India | Indian Genome | Rare Disease India | Genetic Diseases India | Mendelian Disorders India | Genomics India

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Systematic Pharmacogenomis analysis of a Malay whole genome: Proof of concept for personalized medicine - Rare Disease Genomics India - GUaRDIAN | Genomics for Understanding Rare Diseases - India Alliance Network

http://guardian.meragenome.com/publications/systematicpharmacogenomisanalysisofamalaywholegenomeproofofconceptforpersonalizedmedicine

Patient Support and Education. Exome Sequence Analysis and Interpretation. Genetic Diagnosis of Mitochondrial Diseases. I3C - Indian Collaborative on CNS Cavernous Malformations. Clinical Genomics Meeting (ClinGeM). Genomics of Rare Genetic Diseases 2015. Clinical Genomics Meeting (ClinGeM). Gene Ambassador Programme - GAP2016. GenoDerma (03-05 Feb 2017, Pune) - Genomics in Clinical Dermatology. Genomics for Clinicians - Jaipur 2016. Genomics for Personalised and Precision Medicine. Exome sequencing reve...

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

http://guardian.meragenome.com/news-updates/clingemdelhi

Patient Support and Education. Exome Sequence Analysis and Interpretation. Genetic Diagnosis of Mitochondrial Diseases. I3C - Indian Collaborative on CNS Cavernous Malformations. Clinical Genomics Meeting (ClinGeM). Genomics of Rare Genetic Diseases 2015. Clinical Genomics Meeting (ClinGeM). Gene Ambassador Programme - GAP2016. GenoDerma (03-05 Feb 2017, Pune) - Genomics in Clinical Dermatology. Genomics for Clinicians - Jaipur 2016. Genomics for Personalised and Precision Medicine. Exome sequencing reve...

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Genomics for Personalised & Precision Medicine - Rare Disease Genomics India - GUaRDIAN | Genomics for Understanding Rare Diseases - India Alliance Network

http://guardian.meragenome.com/news-updates/genomicsforpersonalisedprecisionmedicine

Patient Support and Education. Exome Sequence Analysis and Interpretation. Genetic Diagnosis of Mitochondrial Diseases. I3C - Indian Collaborative on CNS Cavernous Malformations. Clinical Genomics Meeting (ClinGeM). Genomics of Rare Genetic Diseases 2015. Clinical Genomics Meeting (ClinGeM). Gene Ambassador Programme - GAP2016. GenoDerma (03-05 Feb 2017, Pune) - Genomics in Clinical Dermatology. Genomics for Clinicians - Jaipur 2016. Genomics for Personalised and Precision Medicine. Exome sequencing reve...

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

http://guardian.meragenome.com/patients-care/achondroplasia

Patient Support and Education. Exome Sequence Analysis and Interpretation. Genetic Diagnosis of Mitochondrial Diseases. I3C - Indian Collaborative on CNS Cavernous Malformations. Clinical Genomics Meeting (ClinGeM). Genomics of Rare Genetic Diseases 2015. Clinical Genomics Meeting (ClinGeM). Gene Ambassador Programme - GAP2016. GenoDerma (03-05 Feb 2017, Pune) - Genomics in Clinical Dermatology. Genomics for Clinicians - Jaipur 2016. Genomics for Personalised and Precision Medicine. Exome sequencing reve...

5

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

http://guardian.meragenome.com/home

Patient Support and Education. Exome Sequence Analysis and Interpretation. Genetic Diagnosis of Mitochondrial Diseases. I3C - Indian Collaborative on CNS Cavernous Malformations. Clinical Genomics Meeting (ClinGeM). Genomics of Rare Genetic Diseases 2015. Clinical Genomics Meeting (ClinGeM). Gene Ambassador Programme - GAP2016. Genomics for Clinicians - Jaipur 2016. Genomics for Personalised and Precision Medicine. Hands-on Workshop on Analysis of Human Exome Data. Genomics of Rare Genetic Diseases 2015.

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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...

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Initiatives - India | ORD India

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Helpline : 91 8892 555 000. Email : contactus@ordindia.org. History, Vision and Mission. Donate for a Cause. Physicians & Specialists. Genetic Counselling Centres in India. Initiatives – India. Initiatives – Globally. Initiatives – India. Initiatives – India. Birth Defects Registry of India(BDRI). Lysosomal Storage Disorders Supprot Society. Metabolic Errors and Rare Diseases organization. Association for Social and Health Advancement. Alzheimers and Related Disorders Society Of India. Donate for a Cause.

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Genomics and other omics tools for enabling Medical Decisions (GOMED)

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Uncovering the Hidden Burden of Rare Genetic Diseases in India. Genetic Screening of Dowling-Degos Disease / Galli-Galli Disease. Genetic screening of Lamellar Icthyosis. Genetic testing for Tuberous Sclerosis. Pharmacogenetic testing for 5-Fluorouracil. Pharmacogenetic testing of 5-Fluorouracil. Clinical Genomics Meeting (ClinGem). Genomics for Clinicians - Jaipur 2016. Ute of Genomics and Integrative Biology (CSIR-IGIB). The sequencing of first Indian personal genome. Who benefits from this programme.

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GNE Myopathy

http://gne-myopathy.org/support_group.html

GNE and sialic acid biosynthesis. Clinical features and symptoms. Country specific rules and government support. Family, friend and caregivers. Diagnosis of other Myopathies. It is very important that as GNE Myopathy patients we feel safe in sharing, asking, and discussing issues, and challenges related to GNE Myopathy. Here are some organizations/groups that you may contact for additional support and information. A patient support group in Isreal http:/ www.hibm.org.il/english/.

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Zebrafish Functional Genomics | Sridhar Sivasubbu

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Complete List of Publications. In-Vivo Protein Trap Expression in Zebrafish. Whole Genome Sequencing Initiatives. First Indian Human Genome. First Sri Lankan Human Genome. First Malaysian Personal Human Genome. In collaboration with Dr. Vinod Scaria, CSIR-IGIB). Zebrafish Genome Biology @ CSIR-IGIB. Http:/ zebrafish.igib.in/. Genome of Zebrafish Wild-type Strain(ASWT). Zebrafish Encyclopedia of DNA Elements (ZF-ENCODE). Zebrafish Tissue lncRNA Resource. For Potential Interns and Summer Students. Clark KJ...

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lncRNome: a comprehensive knowledgebase of human long noncoding RNAs - Vinod Scaria MBBS, PhD

http://vinodscaria.rnabiology.org/lncrnome

Open Source Drug Discovery. LncRNome: a comprehensive knowledgebase of human long noncoding RNAs. Bhartiya D,Pal K, Ghosh S, Kapoor S, Jalali S, Panwar B, Jain S, Sati S, Sengupta S, Sachidanandan C, Raghava GPS, Sivasubbu S and Scaria V*. LncRNome: a comprehensive knowledgebase of human long noncoding RNAs.

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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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