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What is Cufflinks?

Cufflinks is a software solution designed to compile transcript data, estimate their relative abundance, and analyze differential expression and regulation within RNA-Seq datasets. By processing aligned RNA-Seq reads, it organizes these into a coherent representation of transcripts. The software evaluates the relative levels of these transcripts using the number of supporting reads while considering biases introduced during library preparation. Originally developed in partnership with the Laboratory for Mathematical and Computational Biology, Cufflinks seeks to streamline the installation process by providing various binary packages that mitigate the often challenging task of building the software from its source code, which typically requires the installation of multiple libraries. This toolset includes several utilities aimed at RNA-Seq experiment analysis, with some features available for standalone use and others designed to integrate into a broader analytical workflow. Furthermore, Cufflinks is essential for genomics researchers, as it significantly enhances their capacity to interpret RNA-Seq data and derive meaningful insights from their experiments. With its user-friendly approach, Cufflinks continues to support advancements in genomic research methodologies.

What is BaseSpace Sequence Hub?

Effective data management and optimized bioinformatics solutions are crucial for labs embarking on or scaling their next-generation sequencing (NGS) efforts. At the heart of the BaseSpace Suite, BaseSpace Sequence Hub acts as a fluid extension of your Illumina equipment. By ensuring secure data transfer from the instrument to BaseSpace Sequence Hub, you can easily manage and analyze your data with a handpicked range of analytical applications. Utilizing Amazon Web Services (AWS) for its infrastructure, BaseSpace Sequence Hub emphasizes data security while enabling you to launch sequencing runs and monitor the performance quality of your devices. The platform increases operational efficiency by converting sequencing data into a uniform format and permitting direct cloud streaming. Moreover, it grants access to computational resources without the burden of heavy investments in local infrastructure. This solution enhances productivity within organizations by offering easy entry to numerous genomic analysis applications developed by Illumina or third-party providers, making it indispensable for any laboratory. Consequently, BaseSpace Sequence Hub not only streamlines laboratory workflows but also promotes innovative advancements and expansion within the field of genomic research. Ultimately, it empowers labs to focus on scientific discovery while minimizing the complexities associated with data management.

Media

Media

Integrations Supported

Amazon Web Services (AWS)
Illumina DRAGEN Secondary Analysis
Pluto
Scispot

Integrations Supported

Amazon Web Services (AWS)
Illumina DRAGEN Secondary Analysis
Pluto
Scispot

API Availability

Has API

API Availability

Has API

Pricing Information

Free
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Cole Trapnell

Date Founded

2017

Company Location

United States

Company Website

cole-trapnell-lab.github.io/cufflinks/

Company Facts

Organization Name

Illumina

Company Location

United States

Company Website

www.illumina.com/products/by-type/informatics-products/basespace-sequence-hub.html

Categories and Features

Categories and Features

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