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IOMICs

iOMICS is a high performance genomics computing platform for analysis and interpretation of multi-Omics data. iOMICS provides applications for sequence data analysis, integrative biology, functional genomics and drug discovery and development such as Drug Target Identification and Validation, Toxicity Analysis & Patient Stratification.


Product Description

Power of supercomputer on a desktop

Private cloud bringing the power of a supercomputer on desktop. Parallel and Distributed algorithms for faster and efficient analysis from start to finish. Easy to store, process, manage data and results in a commercial scale compute and storage center.

Intuitive genome analysis apps

Optimised and interactive apps for diverse sequencing applications. Checkpoint-restart with custom “Reanalyze” options to increase productivity and accuracy. Cohort level analysis options for multiple samples.

Dynamic visualisation features

Dynamic visualisation and result representation features. Click-on navigation to relevant reference databases from result windows for advanced data mining. Integrated genome browser for result visualization.

Supports 3rd party tools

Scalable platform allowing easy integration of custom and 3rd party tools. iOMICS Enterprise version can be customised to suit specific analysis needs by integrating in-house or 3rd party tools, software pipelines or databases.

Features

Genetic Knowledge Base: Omnia

High quality proprietary knowledge base with curated Omics records for biomarker annotation. Contains data collected from multiple data sources, capturing disease related variants, gene expression, epigenomic, protein-protein interaction, metabolic, gene ontology and pathway information. Currently Omnia contains over 100,000 high-quality disease mutations.

Analytics for Knowledge Discovery

Integrates multi scale Multi-Omics data, along with Omnia data, to understand the disease etiology, right from the genomic to the phenotype scale. It can be used to perform advanced disease analytics such as phenotype modeling, drug target identification and validation, and biomarker identification for disease prediction, prognosis, and Pharmacogenomics. It aids in reducing cost, improving turn around time, and a better success rate of drug discovery.

Best-in-class Cloud Technology

It is easy to analyze terabytes of genomics datasets without the need for in-house high performance computing hardware systems. Cloud implementation enables improved accessibility, automatic software updates, convenient pay-per use model, easy data sharing and remote accessibility.

Multi-Omics Data Analysis

Individual datasets from different technologies such as targeted gene seq, Whole EXOME-Seq, DNA-Seq, RNA-Seq, ChIP-Seq and Microarrays can be analyzed. It also supports the integration of Multi-Omics datasets to discover the genetic flow of information associated with the phenotypes.

Experiment Type

It supports multiple experiment types such as a tumor with matched normal pairs, family based analysis and case – control studies.

Applications

Multiple genome analysis apps to choose from

NGS Apps

  • EXOME-Seq
  • DNA-Seq
  • RNA-Seq
  • miRNA-Seq
  • ChIP-Seq
  • HLAScape
  • RAD-Seq
  • Metagenome

Integrative Biology Apps

  • ChIP-RNA
  • DNA-RNA
  • miRNA-RNA

Microarray Apps

  • ChIP-chip
  • Gene-Expression
  • miRNA-Expression

Functional Genomics Apps

  • Functional Enrichment
  • QTL

Drug Discovery and Development Apps

  • Drug Target Identification and Validation
  • Toxicity Analysis
  • Patient Stratification

Ordering Information

iOMICSTM – On cloud
iOMICSTM -On Premise