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

In PLOS this week: effect of variants linked to body shape differs by age and sex, transcriptome differences in bats with and without white-nose syndrome, and more.

A researcher argues that big prizes like the Nobel or Lasker awards send the wrong message about research.

Maria Freire, the president of the Foundation for the National Institutes of Health, discusses recent genomics-fueled advances with The Open Mind's Alexander Heffner.

Three researchers win the Nobel Prize for their efforts to develop treatments for parasitic diseases.

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Personal Genome Diagnostics

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.