The Ethical, Legal and Social Implications (ELSI) Working Group was established for the development of the ELSI component of the Human Genome Project. The Ethical, Legal, and Social Implications (ELSI) program was founded in as an integral part of the Human Genome Project. The mission of the ELSI. ELSI grants also fund education in the science and the social implications of the genome project. A joint NIH-DOE working group has been established.

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What is ELSI? | EMBL-EBI Train online

The purpose of GWAS is twofold:. Explore the connection between specific genes genotype and their outward expression phenotype. This program ensured that potential ethical problems could be resolved as early as possible, before the information was placed into medical applications.

Genome-wide association studies GWAS are used to analyze genetic differences between people with specific illnesses and healthy individuals. As long as the HGP information is being used in medical applications, ELSI will continue to play a large part in preparing that information with guidelines for use on the public and how to prevent abuse of that knowledge.

These potential ethical problems included: Search this Guide Search. Among other topics, this guide covers gene patenting. Examples of topics that fall under such ELSI programs include: Jan 25, 5: Rpoject of Genome Research This guide provides resources that will help the user understand the ethical, legal, and social implications ELSI of genome research–research into the genomes of humans, plants, and other organisms.


Ethical, Legal, and Social Implications (ELSI) of Genome Research: ELSI of Genome Research

Genetic research issue s – projwct area focuses on ethical issues such as “informed consent” written permission from the person being treated and analyses genetic researchers’ aims, methods, and reports of their results. Help identify genetic risk factors for the development or progression of specific illnesses.

Gene patenting – the issues surrounding the legal procedure of claiming “ownership” of a particular gene or region of DNA.

Does “improving” someone’s life include disease symptom reduction or cosmetic improvement e. Explore huamn connection between specific genes genotype and their outward expression phenotype 2.

The Human Genome Project – What are the consequences?

The purpose of GWAS is twofold: The HGP is often called the cure for geonme genetic diseases, because now they elso use its information for treatment in medical care. Examples of topics that fall under such ELSI programs include:.

Fairness in its use by the public – schools, employers and insurance companies must be sensitive to the genetic information and must not unfairly judge individuals based on their genetic status. Home What is Genomics?

This is called “genetic discrimination”. Ethical issues concern what is morally correct and good in the world, gfnome issues talk about how the law should protect the public’s rights and social issues outline prpject ALL of society will be affected by events.

Education – this provides ordinary people with knowledge on genetics and relates ELSI issues to health professionals, policy makers and the general public. Genetic Variation – Self-perception and society’s perception of individuals based on genetic differences Genetic Privacy – Ownership and control of genetic e,si use of genetic information by insurers or employers Gene Patenting – Effect of patenting of DNA sequences on accessibility of data and materials Genes and Illness – Individual susceptibility to specific illnesses, such as cancer Genetically Modified Organisms – Safety of genetically modified foods.


Privacy and equality of genetic data – this program looks into what certain genetic information means as well as stopping information abuse or misinterpretation. However, there are many questions raised about the information it produces, such as Is it possible to own something that is present in hjman humans – is a gene present in an individual theirs or does it belong to the person who discovered it? Psychological issues – those specifically associated with being diagnosed with a particular gene Privacy of genetic information – it is unjust for medics e.

New techniques in medicine – this looks at the effects of genetic testing on individuals, families and reports the latest results to medical services.

Genetic testing of adults, children and foetuses – the different methods of genetic testing for each type of individual raises different questions, such as “do parents have a right to screen a child for a disease if the result may affect the child’s mental well-being?