In 1984, Alec Jeffreys developed the technique of DNA fingerprinting in his laboratory at the University of Leicester. These techniques have revolutionised the way that the police solve crimes.
How was DNA first discovered and who discovered it? Read on to find out...
The human brain, in all its staggering complexity, is the product of millions of years of evolution.
The discovery of the structure of DNA by James Watson and Francis Crick in 1953 is one of the most famous scientific discoveries of all time.
How was DNA discovered to be the carrier of genetic information? Read on to find out...
The zebrafish (Danio rerio) has become a popular model organism only relatively recently. It is a tropical fish from the minnow family with a genetic structure surprisingly similar to ours.
Yeast is one of the simplest eukaryotic organisms but many essential cellular processes are the same in yeast and humans. It is therefore an important organism to study to understand basic molecular processes in humans.
Rosalind Elsie Franklin was a British biophysicist and X-ray crystallographer whose fundamental research was critical to Watson and Crick’s discovery of the structure of DNA.
Maurice Wilkins shared the Nobel Prize with Francis Crick and James Watson in 1962 for their joint discovery of the structure of DNA. Naturally reticent, Wilkins didn’t initially stand forward to give his own account of the DNA story so few knew of his direct involvement in the project.
James Watson and his British colleague Francis Crick discovered the double helix structure of DNA. For this fundamental finding James, Francis and Maurice Wilkins were awarded the Nobel Prize for Physiology or Medicine in 1962.
The Sanger Institute takes its name from the double Nobel Prize winner and ‘father of genomics’, Frederick Sanger.
Francis Crick and his American colleague, James Watson, discovered the double helix structure of DNA. For this fundamental finding Francis, James and Maurice Wilkins were awarded the Nobel Prize for Physiology or Medicine in 1962.
Dr Francis Collins led the Human Genome Project from 1993. In his work, he was responsible for discovering the genes mutated in cystic fibrosis and Huntington’s disease. He is currently director of the US National Institutes of Health (NIH).
The origin of modern humans has probably been the most debated issue in evolutionary biology over the last few decades.
In 2003, two years ahead of schedule, scientists announced that the human genome had been sequenced with an accuracy of 99.99 per cent. It was described as ‘the end of the beginning’.
The announcement of the first draft of the human genome on 26 June 2000 was big news.
The entry of Celera Genomics into the human genome sequencing arena in 1998 galvanised the public effort, leading to a race to sequence the human genome.
The Human Genome Project was a pioneer for encouraging open access to scientific research. In 1996, those involved agreed that all new information produced should be made freely available to all within 24 hours.
The Human Genome Project brought scientists together from across the globe. Worldwide collaboration and support was an essential part of the project’s success.
It was a project of such a huge size that no one thought it would be possible at that time, but with the support of key scientists and considerable funding, the Human Genome Project began…
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