RNA-Seq exploration made simple.

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1

Analyze experimental data faster.

Trovomics provides a fast, no-code solution that performs all the necessary steps for upstream processing and downstream analysis of RNA-Seq experiments. Our team of bioinformatics experts have hand selected industry-proven tools to create one robust, standardized pipeline.

  • Quality Control

  • Trim

  • Align

  • Quantify

  • Quality Control

  • Normalization

  • Differential Expression

  • Pathway Enrichment Analysis

  • Volcano Plot

  • Gene Ontology

  • Comparison
    and more

1 Analyze experimental data faster.

2

Draw critical insights using the industry’s best tools.

Trovomics takes the guesswork out of building your workflow. We implement a collection of industry-standard tools wrapped in our expertly designed pipeline for a streamlined experience. We detect your experimental design and guide you through a customizable analysis setup. This process ensures you get the most robust results, tailored to your data.

Our toolstack:

01

FASTQC

Quality check

02

AdapterRemoval

Trims and removes low quality bases

03

HISAT2

Aligns your RNA-Seq reads to a reference genome

04

HTSeq

Quantifies genes

05

DESeq2

Normalization and differential gene expression analysis

06

clusterProfiler

Functional enrichment analysis

07

Gene Ontology

Gene functional annotations

08

Proprietary
Enhancements 

Automations built by our computational biologists

2 Draw critical insights.

3

The power to investigate your own data.

Use the Trovomics visualizer to explore your data through interactive and customized graphs. Discover the most pertinent results from your sequencing data in any of our visualizations.

Everything you need for your next presentation or publication.

With Trovomics, you can dive into your curated data including all your gene lists, gene expression data, statistics, color assignments, sample/gene metadata, and Gene Ontology (GO) results. Then export your customized graph and its auto generated methods that explain exactly how the graph was made. Everything you need, made accessible like never before.

Key features:

  • Quickly perform additional analyses on data to target subsets of samples or genes

  • Easily download all files and images from analysis and visualization

  • Export methods for communicating pipeline methodology and graph generation

3 The power to investigate your own data.

When you need assistance, we’re here at every step.

Help Center Access

Explore self-service options
in our Help Center

We’re committed to providing you the tools you need to analyze and understand your data, while also bridging knowledge gaps in the field of bioinformatics. That’s why we’ve created an information space that includes:

  • Bioinformatics Resources

  • FAQs

  • Support Access

4

Citing Trovomics in your manuscript

Citing software in scientific research is important for both scientists and the tools that they use.

By citing Trovomics in your research, you are helping to ensure its continued development and maintenance. You’re also helping to make it easier for other scientists to use the platform to conduct their research.

To cite Trovomics in publications use:

Raw sequencing data was analyzed and visualized using Rajant Health Incorporated’s Trovomics omics analysis service (www.trovomics.com).

4 Citing Trovomics in your manuscript

Get started with the plan that’s right for you.

View full feature lists and plan comparisons at Pricing & Plans.

Demo Environment

FREE

  • View the platform to familiarize yourself
    with its functionality

  • Work with pre-loaded RNA-Seq experiments, already analyzed

  • Adjust parameters in the visualizer to see how your graphs change

Special early adopter pricing

Basic

$99

User / Month

  • 1 user

  • RNA-Seq analysis (automated data processing & interactive visualizations)

  • 100 Unlimited analysis hours*

  • 25 GB Unlimited storage*

  • 1-on-1 Trovomics consultation (3 hours)

*limited time access for early adopters