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The National Institutes of Health are funded by an international community of scientists called the Human Genome Project. When the Project started, it said it wanted to sequence all the variations of the human genome that had been discovered and created in the past 50 years. In 2013, NIH said 10,900 variations in the human genome could have been created within that time.

While no one knew a complete list of all variations of human DNA until more than 40 years after the first Human Genome Project, the NIH’s goal was to find variants that could increase the odds of developing cancer or other types of disease more quickly and easily.

The program’s ultimate goal was to sequence the entire genomes of all human beings by 2025.

Because so much of DNA is shared among organisms from such a broad family tree, the researchers expected the full array of genetic variation to be discovered in genomes at least as old as humans.

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With a $2.5 billion grant from NIH, the National Institute of Neurological Disorders and Stroke (NINDS) embarked in 2014 to find the answer to that question.

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For several reasons, the team chose not to call the Neandertal people the first people to emerge on the planet. They did not know the full range of genetic variation of such a small sample, in part because of the difficulty getting human DNA from ancient, highly preserved samples of DNA.

And even among them, the analysis showed, the variation was not uniform.

The researchers said that while they did not study the Neandertal genomes with genetic sequencing, they studied more than 1 million genomes from 11 ancient cultures — including those of ancient people from Europe, South America and South Asia — and found that the Neandertals and their genes shared less DNA than other prehistoric cultures.

The research, published in November 2015 in the journal Current Biology, showed

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