Sequencing Technology | GenomeWeb

Sequencing Technology

BTIG and Mizuho downgraded Illumina's stock after it preannounced third quarter revenue estimates that fell short of analysts' average expectations.

The bioinformatics hub for the Qatar Genome project will partner with WuXi NextCode to develop custom applications for the study population.

The lower preliminary revenue was due to lower than expected sales of its desktop instruments and performance in Europe and Asia Pacific.

Three genetically distinct sub-populations appeared when the team sequenced and compared 48 clinical isolates of Plasmodium knowlesi and five lab lines.

Strand provides a standard of care report that includes a handful of genes and IHC markers within eight days, and the full 152-gene report seven to 12 days later.

Assay instrument for detecting optical signals from samples having a controlled optics adjustment system based on the priority statuses of the samples
Bi-directional sequencing compositions and methods
Methods and apparatus for measuring analytes using large scale FET arrays
Massive parallel method for decoding DNA and RNA
Step-up method for COLD-PCR enrichment
Labelled nucleotides

Researchers examine plant and human DNA found on the Shroud of Turin.

In PNAS this week: Plasmodium knowlesi population structure, 'pre-adaptations' in algal ancestors of land plants, and more.

Replication studies that don't quite reflect the original findings underscore the need to better share data, the Wall Street Journal reports.

About two-thirds of proposals to work with select agents are denied — though most proposals that come in don't meet the definition of a restricted experiment, according to an analysis by the Centers for Disease Control and Prevention.

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This webinar will highlight the key considerations and applications of next-generation sequencing for managing non-small cell lung cancer patients using plasma-based approaches. 

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This webinar will discuss the benefits of a rapid targeted next-generation sequencing (TNGS) panel, using dried blood spots, for second-tier newborn metabolic and hearing loss screening and its immediate utility for high-risk diagnostic testing in the neonatal intensive care unit. 

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This webinar will focus on a range of research and clinical applications enabled by improvements in mate pair technology for whole genome sequencing.