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A new technique helps scientists hunt for information thought to be stored in DNA-bound proteins.
A new blood test uses scraps of fetal DNA to piece together a prenatal diagnosis.
The technique was once considered too error-prone to be useful, but a computational fix could bring it into the world of medical research.
Oxford Nanopore’s approach reads longer stretches of DNA at once—and could more accurately spot structural variations linked to certain diseases.
The largest cancer genome sequencing project yet highlights molecular pathways at the heart of an aggressive blood cancer.
What will the next 20 years of research bring? Eric Green, director of the National Human Genome Research Institute, discusses the institute’s vision.
New technology will allow broad screening for prospective parents.
DNA changes could help doctors see if stray cancer cells remain after treatment.
Start-up Complete Genomics reveals three new human genomes.