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 Nature this week: association between genome-wide homozygosity and traits like height and cognitive ability, improved CRISPR-Cas9 editing, and more.

A survey examines how age, political leanings, and more influence how Americans view certain scientific topics, the Associated Press reports.

A researcher who pleaded guilty to making false statements in research reports has been sentenced to four and a half years in prison and must pay $7.2 million back to the NIH.

The BabySeq project to study the risks and benefits of sequencing newborns is underway.

Jul
14
Sponsored by
Agilent Technologies

This online seminar will outline a recent example of the use of molecular barcoding in combination with next-generation sequencing to detect somatic mosaicism in cancer patients.