A method for keeping private genetic information protected when scouring complete human genomes for the presence of disease-associated genes has been developed by Stanford researchers. The “genome cloaking” technique eases many concerns about genomic privacy and potential discrimination based on an individual’s genome sequence.
Using the technique, the researchers were able to identify the responsible gene mutations in groups of patients with four rare diseases; pinpoint the likely culprit of a genetic disease in a baby by comparing his DNA with that of his parents; and determine which out of hundreds of patients at two individual medical centers with similar symptoms also shared gene mutations.
They did this all while keeping 97 percent or more of the participants’ unique genetic information completely hidden from anyone other than the individuals themselves.
Privacy Fears Addressed
Gill Bejerano, associate professor of developmental biology, of pediatrics, and of computer science at Stanford University, said:
“We now have the tools in hand to make certain that genomic discrimination doesn’t happen. There are ways to simultaneously share and protect this information. Now we can perform powerful genetic analyses while also completely protecting our participants’ privacy,” Bejerano says.
The researchers hope that routine implementation of their technique will help individuals overcome any qualms about privacy that may keep them from sharing their genome sequences.
In particular, people may be concerned that DNA sequences or genetic variants currently unassociated with diseases may in the future be linked with as-yet-unidentified increases in risk. Dan Boneh, a professor of computer science and of electrical engineering, said:
“These are techniques that the cryptography community has been developing for some time. Now we are applying them to biology
Basically, if you have 1 million people with genomic data they would like to keep private, this approach lets researchers analyze the data in aggregate and only report on findings that are pertinent. An individual might have dozens of anomalous genes, but the researchers and clinicians will only learn about the genes relevant to the study, and nothing else.”
When the human genome was fully sequenced in 2001, it was hailed as a remarkable achievement. For the first time, the 3 billion nucleotides that encode the approximately 20,000 genes that keep our bodies running smoothly were tidily listed as a string of letters.
Every human, however, has many variations from the published, consensus sequence. These individual differences are what make us unique, but they can also confer increased risk of genetic diseases.
More than 7,000 diseases are caused by variations in the sequence of a single gene. But in order to determine which variations cause the condition, it has been necessary until now to compare the genetic sequences of hundreds or thousands of individuals with and without the disease, letter by letter.
Geneticists (or their computer software) then make a list of all the differences and identify which are found primarily in people with the disease under study but rarely in any unaffected people. Those variations are then considered to be prime disease-causing suspects.
“There is a general conception that we can only find meaningful differences by surveying the entire genome,” says Bejerano. “But these meaningful differences make up only a very tiny proportion of our DNA. There are now amazing tools in computer science and cryptography that allow researchers to pinpoint only these differences while keeping the remainder of the genome completely private.”
In 2008, President George W. Bush signed the Genetic Information Nondiscrimination Act, which prohibits discrimination in matters of health insurance and employment based on an individual’s genetic information. But there are many other arenas in which such discrimination could potentially occur, including the purchase of life or disability insurance or applying for a loan.
Lead authors and graduate students Karthik Jagadeesh and David Wu worked together to adapt a cryptographic approach known as Yao’s protocol and cloud computing for use with human genomes.
A key component of the technique is the involvement of the individual whose genome is to be studied. In particular, each individual encrypts their genome (with the help of a simple algorithm on their own computer or smart phone) into a linear series of values describing the presence or absence of the gene variants under study, without revealing any other information about their genetic sequence.
The encrypted information is uploaded into the cloud and the researchers then use a secure, multi-party computation (a cryptographic technique that ensures the input data remain private) to conduct the analysis and reveal only those gene variants likely to be pertinent to the investigation.
“In this way, no person or computer, other than the individuals themselves, has access to the complete set of genetic information,” says Bejerano.
In each case, the analysis was performed within seconds or minutes with moderate computing power. They hope to extend the technique to include diseases caused by combinations of multiple genetic variants or to handle tens of thousands of sequences such as those found in genome-wide association studies.
Ultimately, the goal is to find the best way to both share the genetic information with researchers while also protecting each patient’s privacy in order to advance medical knowledge.
The work was funded by Stanford University fellowship grants, the National Science Foundation, the Defense Advanced Research Projects Agency, the David and Lucile Packard Foundation, Microsoft, and the Simons foundation.
Karthik A. Jagadeesh, David J. Wu, Johannes A. Birgmeier, Dan Boneh, Gill Bejerano Deriving genomic diagnoses without revealing patient genomes Science 18 Aug 2017: Vol. 357, Issue 6352, pp. 692-695 DOI: 10.1126/science.aam9710