GENOME SEQUENCING – SCI & TECH

News: The ‘Black Death’ causing bacteria’s prehistoric trail has been traced by scientists thanks to advanced gene-sequencing techniques

 

What is in the news?

       Recently, scientists have identified the prehistoric trail of the Black Death causing bacteria by using genome sequences.

 

What is genome sequence?

       An organism’s complete set of DNA is called the genome. Genome sequencing is simply known as determining the complete order of the bases in a strand of DNA.

 

Applications of genome sequencing:

1. Finding vulnerability of the disease:

       The differences between an individual’s genome to the identified average genome can be used to find the susceptibility to a disease.

2. Evaluate rare disorders:

       Genome sequencing has been used to evaluate rare disorders, preconditions for disorders, even cancer from the viewpoint of genetics.

3. Finding genetic disorders:

       It has also been used as a tool for prenatal screening, to investigate whether the foetus has genetic disorders or anomalies.

4. CRISPR technology:

       The technology called Crispr, which relies on sequencing, may potentially allow scientists to repair disease-causing mutations in human genomes.

5. Diagnosing cancers:

       Liquid biopsies, where a small amount of blood is examined for DNA markers, could help diagnose cancer long before symptoms appear.

6. Decoding the virus:

       In public health, however, sequencing has been used to read the codes of viruses.

7. Slow down the virus transmission:

       a group of scientists from M.I.T and Harvard sequenced samples of Ebola from infected African patients to show how genomic data of viruses could reveal hidden pathways of transmission, which might then be halted, thus slowing or even preventing the infection’s spread.

8. Potential treatment of diseases:

       Creating datasets by collecting genomic profiles across the population, allowing to develop greater understanding of causative factors and potential treatments of diseases.

       This can be used to treat rare genetic disorders.

9. Sustainable agriculture:

       Similar benefits will come to agriculture if there is a better understanding of the genetic basis of the susceptibility of plants to pests, insects and other issues hampering productivity.

 

Challenges:

1. Ethical concern:

       Many doctors and field experts have said that this practice is against the ethics of nature and could lead to gene modification or selective breeding.

2. Privacy threat:

       Major issue is that the data collected through this mechanism can be a possible misuse of genetic information.

3. Reinforcing racism:

       The GIP raises concerns about the potential for scientific racism and the reinforcement of stereotypes based on heredity and racial purity.

 

What is the Genome India Project?

       India’s 1.3 billion-strong population consists of over 4,600 population groups, many of which are endogamous.

        The Indian population harbors distinct variations, with disease-causing mutations often amplified within some of these groups.

       Creating a database of Indian genomes allows researchers to learn about genetic variants unique to India’s population groups and use that to customize drugs and therapies.

       It is a scientific initiative inspired by the Human Genome Project (HGP), an international effort that successfully decoded the entire human genome between 1990 and 2003.

       The project was started in 2020, aiming to better understand the genetic variations and disease-causing mutations specific to the Indian population, which is one of the most genetically diverse in the world.

       The project involves the collaboration of 20 institutions across India and is being led by the Centre for Brain Research at the Indian Institute of Science in Bangalore.