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: swapping yeast genes with human orthologs to study conservation of function, and more.

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