Eureka Genomics has launched its low density marker assay service to detect hundreds of variants from thousands of samples using a single lane of an Illumina sequencer. The service is designed to address the gap between traditional array technologies and multiplex PCR and can be used to validate putative markers from genome-wide association studies and to detect SNPs, copy number variations, and methylation status.

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In Science this week: factors influencing retrotransposon integration sites, and more.

A bioethicist argues for the responsible use of germline gene editing.

Some breweries are using DNA-based testing to determine whether unwanted bacteria are affecting their beers, The Verge reports.

Standardized N-of-1 trials will be needed to test out personalized medicines, writes Nicholas Schork from the J. Craig Venter Institute at Nature.