SEATTLE -- Researchers at the University of Washington have assembled the first comprehensive genetic map of an unborn child -- a development that could help usher in a new era of prenatal testing.
By analyzing fetal DNA circulating in the mother's blood, the scientists were able to sequence the baby's genome 18 weeks into the pregnancy. The technique also worked at eight weeks, with slightly lower sensitivity.
Because the approach requires only a blood sample from the mother and saliva from the father, it poses none of the miscarriage risk associated with invasive tests such as amniocentesis. And while most existing prenatal tests are designed to check for single disorders, including Down syndrome, a full-gene scan has the power to reveal a wide range of potential problems before birth, said lead author Jacob Kitzman, a doctoral student in genetics.
"It's much more comprehensive."
The procedure is still several years away from commercialization, project leader Jay Shendure said.
But the UW study, published in the June 6 issue of Science Translational Medicine, marks a significant step forward in technology that's been developing over the past several years -- and which worries some people, said Marcy Darnovsky of the Center for Genetics and Society in Berkeley, Calif.
"I think it's a game-changer," she said. Cheap, safe genome sequencing could give parents the power to practice a kind of eugenics, preselecting children based on desirable traits.
"It could become a routine part of prenatal testing ... which raises questions about what people will do with the information," Darnovsky said.
Shendure cautioned against expecting too much -- at least in the near future. Scientists may be able to sequence the 3 billion DNA units that make up each person's genetic heritage, but they still don't understand the genetic basis of most common diseases.
"The capacity of genomics to generate data is outstripping our ability to interpret it in useful ways," he said.
Read more:
Researchers assemble genetic map of an unborn child