Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
NovoExpress software offers a user-friendly platform for researchers at any expertise level in flow cytometry, facilitating streamlined sample acquisition and analysis. By automating various fluidic operations, it removes tedious and lengthy tasks from the workflow. The system significantly reduces the need for user intervention thanks to its walk-away autosampler feature, along with capabilities for batch analysis, statistical computation, and reporting. This software consolidates sample acquisition and data analysis into a single interface, enhancing user experience. To further boost productivity, users can analyze data as it is being collected, with ongoing sample acquisition occurring simultaneously in the background. The robust compensation tools and straightforward adjustments ensure precise compensation both before and after sample acquisition. Additionally, the batch analysis and reporting functions provide customizable statistical parameters, along with live updates that keep users informed while samples are being processed. Overall, NovoExpress empowers researchers to work more efficiently and effectively in their flow cytometry tasks.
Description
VarSeq is a user-friendly and efficient software designed for conducting variant analysis on gene panels, exomes, and complete genomes. This comprehensive software solution simplifies tertiary analysis, allowing users to effortlessly automate their workflows and examine variants across various genomic contexts. With VarSeq, the complexities of genomic data become more manageable, enabling researchers to easily navigate and interpret results. The software features a robust filtering and annotation system that helps users efficiently process extensive variant datasets. By employing a sequence of filters, you can swiftly refine your variant list to highlight those of greatest relevance. Once you establish effective parameters for your analysis, VarSeq allows you to save your filter configurations, facilitating the application of the same analytical approach to different datasets. This automated workflow can be consistently utilized across multiple sample batches, making VarSeq particularly suitable for high-throughput settings. Additionally, real-time filtering capabilities empower users to rapidly prototype and adjust analysis workflows according to their specific needs, enhancing the overall research experience. As a result, VarSeq significantly streamlines the variant analysis process for genetic studies.
API Access
Has API
No
API Access
Has API
No
Integrations
GenomeBrowse
No
VSClinical
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
Yes
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
Yes
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
No
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
Yes
Vendor Details
Company Name
Agilent Technologies
Country
United States
Website
www.agilent.com/en/product/research-flow-cytometry/flow-cytometry-software/novocyte-novoexpress-software-1320805
Vendor Details
Company Name
Golden Helix
Founded
1998
Country
United States
Website
www.goldenhelix.com/products/VarSeq/
Product Features
Data Analysis
Data Discovery
No
Data Visualization
No
High Volume Processing
No
Predictive Analytics
No
Regression Analysis
No
Sentiment Analysis
No
Statistical Modeling
No
Text Analytics
No