Genome study: 180 million genetic variants found in 9,772 individuals | Current Affairs | Vision IAS
MENU
Home

Periodically curated articles and updates on national and international developments relevant for UPSC Civil Services Examination.

Quick Links

High-quality MCQs and Mains Answer Writing to sharpen skills and reinforce learning every day.

Watch explainer and thematic concept-building videos under initiatives like Deep Dive, Master Classes, etc., on important UPSC topics.

ESC

Daily News Summary

Get concise and efficient summaries of key articles from prominent newspapers. Our daily news digest ensures quick reading and easy understanding, helping you stay informed about important events and developments without spending hours going through full articles. Perfect for focused and timely updates.

News Summary

Sun Mon Tue Wed Thu Fri Sat

Genome study: 180 million genetic variants found in 9,772 individuals

09 Apr 2025
2 min

GenomeIndia Project: Preliminary Findings

Overview

The GenomeIndia project has published its preliminary findings in the journal Nature Genetics, focusing on the genetic diversity among Indians. The study involves genotyping 10,074 healthy and unrelated Indians from 85 populations, which includes both tribal and non-tribal groups.

Data Collection and Methodology

  • Blood samples from approximately 20,000 individuals were collected.
  • Whole genome sequencing was conducted on DNA samples from 10,074 individuals.
  • 85 populations were studied: 32 tribal and 53 non-tribal, across India.
  • The study excluded two populations, focusing on 9,772 individuals (4,696 males and 5,076 females).
  • Data has been deposited in the Indian Biological Data Centre (IBDC) in Haryana.

Genomes Sequenced

  • Tribal groups: Tibeto-Burman, Indo-European, Dravidian, Austro-Asiatic, and a continentally admixed outgroup.
  • Non-tribal groups: Tibeto-Burman, Indo-European, and Dravidian.

Genetic Variants and Their Significance

  • Total genetic variants identified: 180 million.
  • 130 million variants found in autosomes (non-sex chromosomes).
  • 50 million variants found in the sex chromosomes (X and Y).

Research Focus

  • Identifying functionally relevant variants related to diseases, therapeutic responses, and adverse effects.
  • Constructing a panel of variants for future genotyping and disease-genetic correlations.
  • Exploring variants linked to disease susceptibility and environmental adaptations.

Applications

The study aims to utilize genetic information to develop low-cost diagnostic kits and advance personalized medicine. This initiative will enhance disease diagnostics, predict genetic drug responses, and promote precision medicine in India.

Collaborative Effort

  • Involves 20 institutions, with genome sequencing conducted by prominent research centers including IISc Bangalore and others.

Explore Related Content

Discover more articles, videos, and terms related to this topic

Title is required. Maximum 500 characters.

Search Notes

Filter Notes

Loading your notes...
Searching your notes...
Loading more notes...
You've reached the end of your notes

No notes yet

Create your first note to get started.

No notes found

Try adjusting your search criteria or clear the search.

Saving...
Saved

Please select a subject.

Referenced Articles

linked

No references added yet