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The company's goal is to serve what it sees as a massive but underaddressed target group: Asian women.

At Belgium's VIB, researchers have designed custom panels with CNV detection in mind to get better data on single-cell genomic changes during cancer treatment.

The San Diego-based firm has developed a new extracellular RNA sequencing method that it believes could be used for cancer diagnostics.

The company believes that Xdrop will find adopters in academia and clinical research, although diagnostics is on its radar.

The German company's new Genome Enhancer product is an adaptation of its flagship multi-omics software for clinicians and biologists without bioinformatics expertise.

Illumina plans to upgrade all its NIPT customers to version 2 of its VeriSeq solution over the next year.

The firm said it is helping customers convert from SNP genotyping arrays to an NGS workflow, which may allow it to access the ag-bio and direct-to-consumer markets.

The company is hoping to add outreach to make sure individuals who want counseling get it, and to better understand the reasons why others might not.

A collaboration with ATAC-seq experts at the Broad Institute suggests the Bio-Rad assay can analyze tens of thousands of cells per experiment.

New instrument releases at this week's meeting reflected proteomics' increased emphasis on throughput and the continuing spread of ion mobility technology.

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23andMe has a holiday popup shop at a mall and could open additional stores, Bloomberg reports.

By studying koalas and a retrovirus that infects them, researchers may have uncovered a new sort of 'immune response' that occurs at the genomic level, Agence France Presse reports.

NPR reports that the first person in the US given a gene editing-based therapy for a genetic disorder is heading home.

In Science this week: ancient genomes reveal social inequality within individual households, new method for quantifying genetic variation in gene dosage, and more.