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D Rs. 500 Faculty/Scientist Rs. 750 Genetics of Non-Communicable Diseases A future perspective 16th-17th March 2017 Name Designation Student/ Asst. Organisers Dr. R. Malathi Dr. A. K. Munirajan Dr. Chandra R. Samuel Dr. C. R. Srikumari Dr. B. Anandan Dr. 00 am. Venue Dr. A. Venugopal Auditorium Dr. ALM PG IBMS University of Madras Taramani campus Chennai 600 113. UNIVERSITY OF MADRAS DEPARTMENT OF GENETICS The staff and students are pleased to invite you for the DST-PURSE sponsored...
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01
Gather information about the specific non-communicable disease you are studying.
02
Identify the genetic factors associated with the non-communicable disease.
03
Acquire relevant genetic data or samples from individuals with and without the disease.
04
Conduct statistical analysis to determine any genetic variations or mutations that may be linked to the disease.
05
Interpret the findings and draw conclusions about the genetic basis of the non-communicable disease.

Who needs genetics of non-communicable diseases?

01
Researchers studying the genetic basis of non-communicable diseases.
02
Medical professionals and scientists interested in understanding the genetic risk factors associated with these diseases.
03
Patients and individuals at risk of developing non-communicable diseases, to understand their genetic predisposition and potential treatment options.
04
Pharmaceutical companies and drug developers, for designing personalized medicine and targeted therapies based on genetic factors.
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Genetics of non-communicable diseases refers to the study of how genetic factors contribute to the development of chronic conditions such as heart disease, diabetes, and cancer.
Healthcare professionals, researchers, and public health officials may be required to file information on genetics of non-communicable diseases.
To fill out information on genetics of non-communicable diseases, one must gather relevant data on genetic risk factors, disease prevalence, and potential interventions.
The purpose of studying genetics of non-communicable diseases is to better understand the role of genetic factors in disease development, inform prevention strategies, and improve patient care.
Information that may need to be reported includes genetic variants associated with specific diseases, disease prevalence rates, and public health interventions.
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