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Institute 14

Centre for Rare Disease & Genomic Medicine

Families wait seven years for a diagnosis. That is the number we are attacking.

A glass and porcelain double helix with orange molecular connections.

Families wait seven years for a diagnosis. That is the number we are attacking.

Sequencing, counselling and periodic reanalysis operate as one undiagnosed-disease programme. A report is not the end of the pathway.

A clinical sequencer beside three sample vials and a restrained base-call trace in an empty genomics laboratory.
Centre for Rare Disease & Genomic Medicine Aristion

What's in it.

Phase I · sequencing and counselling / Phase II · functional genomics

Institute 1405 connected clinical parts
A glass and porcelain double helix with orange molecular connections.

Whole-genome sequencing

One clinical system

What we intend to research here

Unsolved-case reanalysis and Indian rare-disease registries.

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