Rajant Health, Inc.
Trovomics is a web-based bioinformatics platform for RNA-Seq analysis that provides an automated, no-code pipeline for upstream processing and downstream analysis, plus interactive visualization tools and support resources. The service includes server-side processing, data export for publication, and access to consultations with in-house computational biologists. The project is associated with Rajant Health Incorporated and aims to expand to additional omics and precision-medicine data integration.
Industries
N/A
Nr. of Employees
small (1-50)
Rajant Health, Inc.
Patents
Products
RNA-Seq analysis and visualization platform
A web application that performs automated upstream and downstream RNA-Seq analyses and provides interactive, exportable visualizations and auto-generated methods text for reproducibility and publication.
Lossless FASTQ/A compression algorithm
A reference-free, lossless compression algorithm for FASTQ/FASTA files that preserves nucleotide codes and read identifiers and adapts compression to file structure to reduce storage and transfer costs.
RNA-Seq analysis and visualization platform
A web application that performs automated upstream and downstream RNA-Seq analyses and provides interactive, exportable visualizations and auto-generated methods text for reproducibility and publication.
Lossless FASTQ/A compression algorithm
A reference-free, lossless compression algorithm for FASTQ/FASTA files that preserves nucleotide codes and read identifiers and adapts compression to file structure to reduce storage and transfer costs.
Services
Web-based demo account with pre-loaded RNA-Seq experiments allowing users to explore visualizer controls and adjust parameters without time limits.
Tiered subscription service providing RNA-Seq analysis, interactive visualizations, storage and analysis hours, and consultation hours; Basic targets individual researchers, Pro and Enterprise target teams with admin and management features.
Personalized sessions with computational biologists to advise on experiment design, analysis parameters, visualization strategy, re-analysis, and interpretation; consultation hours included in subscription tiers.
Web-based demo account with pre-loaded RNA-Seq experiments allowing users to explore visualizer controls and adjust parameters without time limits.
Tiered subscription service providing RNA-Seq analysis, interactive visualizations, storage and analysis hours, and consultation hours; Basic targets individual researchers, Pro and Enterprise target teams with admin and management features.
Personalized sessions with computational biologists to advise on experiment design, analysis parameters, visualization strategy, re-analysis, and interpretation; consultation hours included in subscription tiers.
Expertise Areas
- RNA-Seq data analysis
- Bioinformatics pipeline development
- Interactive omics data visualization
- Functional enrichment and Gene Ontology analysis
Key Technologies
- Next-generation sequencing (RNA-Seq)
- FASTQ/FASTA file handling
- FASTQC
- Adapter trimming tools
News & Updates
Description of a lossless, reference-free compression algorithm for genomic FASTQ/A files designed to reduce storage and transfer costs without losing information.
Timing breakdown and example demonstrating pipeline performance, including an example end-to-end run completed in under 48 minutes for a 24-file dataset.
Background on barriers to bioinformatics adoption and a rationale for a no-code, interactive RNA-Seq analysis and visualization platform aimed at accelerating research.
Article discussing precision medicine and the role of genomic, proteomic, and metabolomic data and technologies such as NGS, AI, and cloud computing in delivering targeted therapeutics.
Description of a lossless, reference-free compression algorithm for genomic FASTQ/A files designed to reduce storage and transfer costs without losing information.
Timing breakdown and example demonstrating pipeline performance, including an example end-to-end run completed in under 48 minutes for a 24-file dataset.
Background on barriers to bioinformatics adoption and a rationale for a no-code, interactive RNA-Seq analysis and visualization platform aimed at accelerating research.
Article discussing precision medicine and the role of genomic, proteomic, and metabolomic data and technologies such as NGS, AI, and cloud computing in delivering targeted therapeutics.