NIST Researcher Looks Toward the Future of Rapid DNA

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NIST researcher Erica Romsos’ research is helping to make Rapid DNA technology more effective. Credit: Megan King/NIST

by Erica Romson, Research Biologist, Applied Genetics Group, NIST

DNA samples are typically processed in a laboratory under very strict protocols. There are multiple review steps to ensure accuracy. That process can take from eight hours to a few days, depending on the sample. Sometimes, law enforcement needs results much faster. This is where Rapid DNA technology comes in, providing results in as little as 90 minutes.

But speed cannot come at the expense of quality. I focus on making sure these quick results meet strict accuracy standards, so law enforcement officers know they’re getting the correct information quickly.

How Rapid DNA works

Rapid DNA is often used to identify people who have been arrested or victims in mass casualty events, such as plane crashes, wildfires and building collapses. In some cases, it can be used in traditional DNA casework, such as murder investigations.

The Rapid DNA equipment is about the size of a standard office printer, more compact than laboratory equipment. The user (typically law enforcement) collects a sample with a cotton swab and places it into a specialized cartridge inside the machine. The machine extracts the DNA, creates many labeled copies, and then separates those copies to create a person’s profile, or genetic fingerprint.

The Rapid DNA systems use two types of cartridges to create a profile. One is for high-quality, high-volume DNA, such as what you would find in a cheek swab. A cheek swab is a controlled collection process that yields higher-quality DNA samples.

A different type of cartridge is used for forensic evidence, such as blood found at a crime scene. These types of samples are much more challenging. In these cases, the quality and amount of DNA are much lower.

Testing Rapid DNA

If the DNA samples meet the FBI’s strict quality requirements after analysis, law enforcement works with a lab to upload them to the National DNA Index System (NDIS). This database helps solve crimes and identify missing and unidentified people. But how can users know that the equipment they use to analyze DNA samples actually meets the FBI’s strict standards?

That’s where NIST comes in. Our work provides the criminal justice community with confidence that the equipment they rely on is accurate.

We also help law enforcement and lab professionals determine the tools’ limitations, including which types of evidence are suitable for Rapid DNA testing. DNA from multiple people, for example, should go to a traditional crime lab, not a Rapid DNA instrument.

NIST is uniquely suited for this role. This is not just because of our scientific expertise, but because we are a neutral, unbiased source focusing on the measurement itself.

One of my primary roles is to facilitate interlaboratory studies. In these studies, multiple laboratories test the same material using identical methods to ensure consistent, accurate results.

We’ve recently finalized an interlaboratory study examining both pristine DNA samples (easier to test) and mixed DNA samples from multiple people (harder to test) using new Rapid DNA cartridges. We prepared samples, collected and analyzed data, and made our results available to the public. Our study helped inform the FBI standards that crime laboratories must follow for Rapid DNA.

Looking ahead

One challenge of studying Rapid DNA is that the process consumes the entire sample. So, an officer or technician puts the sample into the cartridge, gets one shot at the test, and doesn’t get that sample back for any further analysis.

The problem is — lots of things can go wrong. The machine could fail. The power could go out at the exact moment they’re testing that sample, and then the sample is gone forever.

Additionally, some states have laws requiring samples to be saved in case a defense attorney requests retesting.

I’m currently studying how we can potentially preserve those samples used in the Rapid DNA process. I’m doing this by exploring how we could create duplicate samples from a single original sample while retaining the same DNA profile and quality. We call this subsampling.

Subsampling to preserve the original sample would help law enforcement use Rapid DNA while still complying with state laws on sample preservation. It would also enable law enforcement to use Rapid DNA for investigative leads while sending the original sample to the laboratory.

I continue to work to bridge the gap between the speed of the field and the rigors of the lab. That’s because it’s vital that forensic science remains reliable and accurate and that any limitations in the systems are identified and addressed.

About the author

Erica Romsos is a research biologist with the Applied Genetics Group at NIST, focusing on rapid DNA testing, digital PCR analysis and standards development. Her work in standard reference material (SRM) characterization has assisted with the creation of many SRMs produced by NIST for the forensic DNA community. Additionally, Erica is the leader of the Forensic Science Quality Assurance Program, supporting method testing, validation and technology performance across different forensic science disciplines.

Republished courtesy of NIST



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