Writing
Selected notes on rare-disease diagnostics, national genomics programmes, and work from the laboratory and clinic.
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A Tata Trusts Horizons perspective on rare genetic diseases in India — diagnosis, families, and national policy — from the diagnostics work at CDFD.
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INDVar is live: an Indian genomic variant database
A national resource that lists disease-causing variants, variants of uncertain significance, and phenotype data from affected individuals in India.
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Notes from the President’s At Home reception on the 80th Independence Day.
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PRaGeD and structured genomic data
The paediatric rare-disease mission is moving toward unified clinical and genomic records across centres.
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Cytogenetics and chromosomal microarray workshop, Hyderabad
A hands-on workshop at CDFD, 5–9 October 2026, on cytogenetics and chromosomal microarray.