Meet the system we designed just for you.
Created by biologists for life science researchers, the Maverix Analytic Platform integrated everything you need to analyze, visualize, explore and manage your NGS data in an easy-to-use system without the need for bioinformatics expertise or large-scale computing infrastructure.
- Quick and easy uploading of your NGS data
- Powerful, industry-standard open source tools
- Ready to use, carefully constructed pre-configured pipelines
- Sharing and collaboration
- Integration of public and private data sets to add context
- On-demand computing power and storage to rapidly scale to almost any size project
- Pay-per-sample pricing scales with your project needs
- Custom service development
The Maverix Analytic Platform integrated everything you need to manage, explore, and visualize genomic data
Platform-as-a-Service Offerings
Pre-configured Analysis Kits
- Start analyzing your data as soon as it is ready, using the same methods as other leaders in the field have published in their papers
DNA sequencing and analysis using NGS has become a powerful tool in biomedical research. It has given us the ability to understand and diagnose genetic disorders, investigate genetic predispositions for cancer, and explore the relationship between genotype and phenotype. Due to advancements in technology it is now possible to use sequencing as a rapid means of diagnosing illness and formulating a treatment. However, data analysis and interpretation can still be an important challenge in this field.
RNA-seq is a high-throughput sequencing technology that provides a genome-wide assessment of the RNA content of an organism, tissue or cell. mRNA-seq can be used to measure gene expression levels, assist in new gene and transcript discovery, and identify novel splice variants. Our mRNA-Seq analysis uses open-source tools, including a de novo splice aligner, either TopHat or STAR, in conjunction with Cufflinks to elucidate the transcriptome and analyze differential expression. The analysis results are provided as visual representations, including interactive tabular and heat map views linked to an integrated genome browser.
Small RNA-seq is a method for analyzing the expression of small noncoding RNAs. These small ncRNAs include microRNAs, snoRNAs, piRNAs, small antisense transcripts, etc. Novel ncRNA discovery, transcription start site detection, as well as small RNA regulatory pathways can be studied through the use of small-RNAseq.
Released by multiple cell types and found in many body fluids, including plasma, breast milk and saliva, exosomes are extracellular vesicles of endosomal origin that contain protein, lipids, mRNA, microRNAs and many types of small non-coding RNAs. This analysis kit is designed to elucidate the exosome transcriptome using next generation sequencing, and to analyze differential expression and facilitate small RNA discovery.
Life science researchers can find accessing the benefits of Next Generation Sequencing to be a daunting task: researching and selecting multiple vendors; moving samples and data through multiple processing steps. Our Maverix Complete solution simplifies this complex decision-making process and offers a streamlined one-stop approach that allows researchers to spend their time where it may count the most—interacting directly with the data that will ultimately advance their research and likely accelerate their understanding of biological processes and diseases. Maverix Complete combines samples preparation, sequencing services, secondary and tertiary data analysis into a single process managed by Maverix that makes it easier, faster and more cost effective for you to gain meaningful insight from NGS projects.
Custom Service Development
- Dedicated scientists and bioinformaticians for pipeline and customer application development
The custom services offered by Maverix Biomics utilizes in-house expertise to test a range of possible pipelines in order to find the most suitable analysis pipeline for each situation which can then be automated into their easy-to-use, secure platform to run the customized pipeline at scale. Once an automated version is produced and validated, training is provided along with a dedicated and secure on-line access to ensure a smooth transition and on-going ease of use.
| Feature | Benefit |
|---|---|
| Designed to be easy for researchers to use directly for data management, analysis, and visualization | Eliminates “bioinformatician bottleneck” and shortens time to discovery |
| Pre-defined analysis pipelines, based on peer-reviewed, open source methods with reference data sets | Start analyzing your data as soon as it is ready, using the same methods as other leaders in the field have published in their papers |
| Pay-as-you go pricing - charged per sample | Only pay for what you use, when you use it |
Simple. Accepted. Efficient. Affordable.
Revolutionize the way you analyze your NGS data by integrating proven, open-source software and algorithms in a high performance cloud-based environment that is designed for ease of use by any biologist.