The
high-quality genomes will be made freely available to scientists to use in
their research
Date: October 3, 2018
Source: Wellcome Trust Sanger Institute
The
genomes of 25 UK species have been read for the first time by scientists at the
Wellcome Sanger Institute and their collaborators. The 25 completed genome
sequences, announced today (4 October) on the Sanger Institute's 25th
anniversary, will lead to future studies to understand the biodiversity of the
UK and aid the conservation and understanding of our species.
The
newly-sequenced genomes will enable research into why some brown trout migrate
to the open ocean, whilst others don't, or investigations into the magneto
receptors in robins' eyes that allow them to 'see' the magnetic fields of
Earth. The genomes could also help to shed light on why red squirrels are
vulnerable to the squirrel pox virus, yet grey squirrels can carry and spread
the virus without becoming ill.
The
Sanger Institute was founded in 1993 by Professor Sir John Sulston as part of
the Human Genome Project. The Institute made the largest single contribution to
the gold- standard sequence of the first human genome, which was published in
2003.
A genome
is an organism's complete set of genetic instructions written in DNA. Each
genome contains all of the information needed to build that organism and allow
it to grow and develop.
Since the
landmark completion of the human genome, the Sanger Institute has become a
globally recognised leader in the field of genomics. Many more important
reference genomes have already been sequenced -- from the mouse and zebrafish
genomes to the pig, gorilla, mosquito and many others. Beyond animal species,
infectious diseases and bacteria also feature prominently on the list of
reference genomes, from salmonella and MRSA to chlamydia and malaria. All of
these have offered up important insights about these species in health and
disease.
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