The survey, conducted by Bank of America Merrill Lynch and GenomeWeb, found that almost half of current NGS users plan to add new systems over the coming year.
The company was founded earlier this year based on an improved method for multiple displacement amplification and a single-cell-variant caller.
Contrary to Illumina's reports that index switching is rare, the Stanford team found the issue occurred in more than 5 percent of sequence reads.
The firm is in the process of commercializing an open, optimizable, high-throughput library preparation instrument for single-cell transcriptome profiling.
These cell subtypes could help researchers gain a clearer understanding of cell mechanics and find better targets for potential therapies.
Mary Beckerle has been removed as director of the Huntsman Cancer Institute in what one researcher refers to as a "coup," ScienceInsider reports.
Bill Gates tells the Telegraph that bioterrorism is a serious risk.
The March for Science is to take place tomorrow, and supporters are tapping their creative energies to create placards to carry.
CBS News reports that the White House Science Fair is to continue under President Donald Trump.
This webinar is the third in a four-part series highlighting real-world examples of how some lab directors are bringing validated next-generation sequencing-based tests to the clinic.
This webinar is the last in a four-part series highlighting real-world examples of how some lab directors are bringing validated next-generation sequencing-based tests to the clinic.
This webinar will provide an overview of an RNA-seq protocol that has been optimized to study small RNA species such as microRNAs.
This webinar will discuss a target enrichment workflow for high-confidence detection of variants.