Position Statement of the Indian Academy of Medical Genetics on Next Generation Sequencing-Based Testing for Rare Genetic Disorders
Next-generation sequencing (NGS)-based tests are being increasingly employed by clinicians for obtaining a genetic diagnosis in individuals and families with possible genetic disorders. However, there is a significant disparity in the genomic knowledge and skills of the clinicians employing these tests for care and management of families with rare genetic disorders. Through the current document, the Society for Indian Academy of Medical Genetics (SIAMG) aims to provide guidance and consideration in terms of the type of tests available, their appropriate applications, and result interpretation in order to make judicious use of these tests for rare disease diagnosis.
Authors
- Prajnya Ranganath (ORCID: https://orcid.org/0000-0001-7122-3197)
- Deepti Gupta (ORCID: https://orcid.org/0000-0002-1349-1510)
- Mounika Endrakanti
- Anju Shukla (ORCID: https://orcid.org/0000-0003-2471-4094)
- Amita Moirangthem (ORCID: https://orcid.org/0000-0003-0756-9868)
- Sameer Bhatia
Institutions
- Nizam's Institute of Medical Sciences (IN)
- Sanjay Gandhi Post Graduate Institute of Medical Sciences (IN)
- Manipal Academy of Higher Education (IN)
- Noida International University (IN)
- Sir Ganga Ram Hospital (IN)
- All India Institute of Medical Sciences (IN)
Publication Details
- Journal
- The Indian Journal of Pediatrics
- Published
- 2026-06-16
- DOI
- https://doi.org/10.1007/s12098-026-06124-w
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00