Why in the News?

India has created a database of 10,000 human genomes, covering 83 population groups, which is about 2% of the country’s 4,600 population groups.

What are the key achievements of the Genome India Project?

Completion of Genome Sequencing: The project successfully sequenced 10,000 human genomes from 83 population groups, representing approximately 2% of India’s 4,600 population groups. This data is now housed at the Indian Biological Data Centre (IBDC) in Faridabad, Haryana.
Identification of Genetic Variants: Initial analyses revealed around 27 million genetic variants, with 7 million being low-frequency variants not found in other global databases. This highlights India’s unique genetic diversity and the potential for targeted research.
Global Accessibility: The genome data is accessible to researchers worldwide, fostering international collaboration in genomics research and precision medicine.

Advancement of Precision Medicine: The database is expected to facilitate advancements in precision medicine by enabling researchers to study disease risks and drug responses specific to the Indian population. This could lead to more effective treatments tailored to genetic variations.
Potential for Drug Development: With a focus on understanding genetic predispositions to diseases, the project can support the development of new medications and therapeutic interventions, particularly for genetic and infectious diseases.
Strengthening India’s Biotech Economy: The initiative is seen as a cornerstone for bolstering India’s biotechnology sector, enhancing its capacity for genomic research and manufacturing.

Data Privacy and Security: India currently lacks a comprehensive Data Privacy Bill, which raises concerns about the protection of sensitive genetic information.
- The absence of robust legal frameworks increases the risk of misuse or unauthorized access to genetic data, potentially compromising individual privacy.
Ethical Concerns: The use of genomic data for purposes such as gene editing could lead to ethical dilemmas, including issues related to “designer babies” and unintended consequences of genetic modifications.
Public Trust and Acceptance: Gaining public trust is crucial for the success of the project. There may be apprehensions among individuals regarding how their genetic data will be used, especially if it involves sharing with commercial entities or if there are fears about potential discrimination based on genetic information.
Integrity of Data Collection: Ensuring the integrity and accuracy of data collection, storage, and usage is essential.
- Without stringent protocols, there is a risk that the data may be misinterpreted or misused, leading to flawed conclusions about genetic predispositions and health risks.

Expanding the Database: Experts suggest increasing the number of sequenced genomes to up to 1 million to better capture India’s vast genetic diversity. This expansion would provide deeper insights into genetic variations across different ethnic groups.
Funding and Collaboration: Securing additional funding and forming partnerships with leading research institutions can help overcome financial limitations and enhance data enrichment efforts.
Ethical Data Management: Ensuring robust data sharing protocols and privacy measures will be crucial for maintaining public trust and facilitating research access while protecting individual identities.