"Two years ago, NIST hosted Genome in a Bottle--a group that includes stakeholders from industry, academia and the federal government--to develop reference materials that could measure the performance of equipment, reagents and mathematical algorithms used for clinical human genome sequencing," says NIST biomedical engineer
Modern DNA sequencers take a genetic sample in the form of long strings of DNA and randomly chop the DNA into small pieces that can be individually analyzed to determine their sequence of letters from the genetic alphabet. Then, bioinformaticians apply complex mathematical algorithms to identify from which part of the genome the pieces originated. These pieces can then be compared to a defined "reference sequence" to identify where mutations have occurred in specific genes.
There are several different DNA sequencing technologies and computer algorithms to do this very complex analysis, and it's known that for any given sample, they will produce similar, but not identical results. Built-in biases as well as what are essentially "blind spots" for certain possible sequences contribute to uncertainties or errors in the sequence analysis. "These biases can lead to hundreds of thousands of differences between sequencing technologies and algorithms for the same human genome," Zook says. In a recent paper in Nature Biotechnology,* Zook and his colleagues describe the methods used to make the Genome in a Bottle consortium's pilot set of genotype reference materials. The source DNA, known as NA12878, was taken from a single person. The reference set is essentially the first complete human genome to have been extensively sequenced and re-sequenced by multiple techniques, with the results weighted and analyzed to eliminate as much variation and error as possible.
"We minimized bias in our reference materials toward any specific DNA sequencing method by comparing and integrating data from 14 sequencing experiments generated by five different sequencing platforms," Zook says. The findings in the Nature Biotechnology paper are publicly available from the Genome in a Bottle website, www.genomeinabottle.org. In addition, the Genome Comparison and Analytic Testing (GCAT) website enables real-time benchmarking of any DNA sequencing method using the paper's results. The research was conducted by a team of scientists at NIST;
For more information on the Genome in a Bottle consortium, go to www.genomeinabottle.org.
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