Skip to main content

Sentient Suite, GenBank 164.0, StarDrop

Premium
IO Informatics has released a new version of its Sentient Suite integration platform, which includes new capabilities based on semantic technology. The platform includes Sentient Knowledge Explorer, which uses semantic web technology “to integrate, model, visualize and explore data, revealing networks and novel relationships in complex data sets from one or multiple sources,” the company said. Sentient Suite also includes Web Query, Process Manager, and Data Manager modules.
 

 
GenBank 164.0 is available via FTP from the National Center for Biotechnology here.
  
The new release contains 85,759,586,764 base pairs of non-whole-genome-shotgun sequence and 108,635,736,141 base pairs of WGS sequence. Uncompressed, the 164.0 release flat files require about 321 GB for sequence files only. The ASN.1 data require approximately 295 GB.
 

 
BioFocus DPI has launched StarDrop (structure-activity relationships for drug optimization), an upgrade to the company’s ADMEnsa Interactive package. BioFocus said that it has expanded the software “beyond the prediction of ADME properties to include interactive data visualization and compound modeling for effective decision making.”
 
StarDrop integrates in silico predictions with in vitro and in vivo data to help researchers design, prioritize, and select compounds “with an optimal balance of properties,” the company said.

Filed under

The Scan

Response Too Slow, Cautious

A new report criticizes the global response to the threat of the COVID-19 pandemic, Nature News reports.

Pushed a Bit Later

Novavax has pushed back its timeline for filing for authorization for its SARS-CoV-2 vaccine, according to Bloomberg.

AMA Announces Anti-Racism Effort

The Associated Press reports that the American Medical Association has released a plan to address systemic racism in healthcare.

Nucleic Acids Research Papers on miRMaster 2.0, MutationTaster2021, LipidSuite

In Nucleic Acids Research this week: tool to examine small non-coding RNAs, approach to predict ramifications of DNA variants, and more.