Average Ratings 0 Ratings

Total
ease
features
design
support

No User Reviews. Be the first to provide a review:

Write a Review

Average Ratings 0 Ratings

Total
ease
features
design
support

No User Reviews. Be the first to provide a review:

Write a Review

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

API Access

Has API

Screenshots View All

Screenshots View All

Integrations

GenomeBrowse
VSClinical

Integrations

GenomeBrowse
VSClinical

Pricing Details

No price information available.
Free Trial
Free Version

Pricing Details

No price information available.
Free Trial
Free Version

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

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
Data Visualization
High Volume Processing
Predictive Analytics
Regression Analysis
Sentiment Analysis
Statistical Modeling
Text Analytics

Alternatives

Alternatives

Emedgene Reviews

Emedgene

Illumina
OmicsBox Reviews

OmicsBox

BioBam Bioinformatics S.L.
QIAGEN CLC Genomics Workbench Reviews

QIAGEN CLC Genomics Workbench

QIAGEN Digital Insights
GenomeStudio Reviews

GenomeStudio

Illumina