AFTER a series of well-publicised drafts, at last we have it: the final, all singing, all dancing, gold-standard edition of the human genome. It is now as complete as it can be with existing technology, researchers announced earlier this week in Bethesda, Maryland.
“It’s the first and only edition of the book of life, and everything before it was simply a draft,” says Francis Collins, director of the US’s National Human Genome Research Institute in Bethesda, and the head of the 2500-strong international team of researchers at 16 centres around the world who did the sequencing.
Unlike the earlier drafts, there are no substantial holes left in the string of 3 billion base units that make up our 24 chromosomes. “There are still gaps that are [currently] unsequenceable, but it’s only about 1.5 per cent,” says Collins. “That’s what we called the finishing line when we began this enterprise, and now we’ve done it.”
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The completed sequence eclipses all the previous and much-hyped “launches” of the genome, including the first draft hailed by Bill Clinton in November 2000 as “the most wondrous map ever produced”. And it is freely available on the web. “We can now declare victory for this endeavour,” says Collins, a task which has taken 13 years. “I’d say I’m exhilarated.”
But researchers still have to wait for the full analysis and annotation of the sequence which could take a year. Collins says the genome teams are still discussing timing, but they intend to publish papers on each individual chromosome sequenced.
In a 13-page feature that will appear in next week’s Nature, Collins outlines the challenges ahead. As analyses of our genes roll in, along with the proteins they produce and their chemical structures, he warns that we need to avoid the patenting nightmares that beset the task of sequencing. “We may be headed for a rerun if we’re not careful. This time we need to be more pro-active.”