IPA has a broad set of features that allow you to quickly understand and visualize your data
Causal Network Analysis* new
The new Causal Network Analysis provides a comprehensive approach to identifying upstream molecules that control the expression of the genes in your datasets. Expanding beyond "direct" or "single hop" relationships between the upstream regulator and the target molecules in the dataset, Causal Networks uncovers networks of regulators that connect to the dataset targets. Focus on the networks that are of highest relevance by scoring the resulting causal networks against molecules or diseases/functions of interest.
Comparison Analysis new
Quickly visualize Canonical Pathway score trends across dose, time, or other factor using the new heat map. Prioritize by score, hierarchical cluster, or trend.
BioProfiler* new
Quickly profile a disease or phenotype by understanding its associated genes and compounds. Identify genes known to be causally relevant as potential targets or identify targets of toxicity, associated known drugs, biomarkers and pathways.
Upstream Regulator Analysis
Predict upstream molecules, including microRNA and transcription factors, which may be causing the observed gene expression changes.
Mechanistic Networks
Automatically generate plausible signaling cascades describing potential mechanism of action leading to observed gene expression changes.
Downstream Effects Analysis
Identify whether significant downstream biological processes are increased or decreased based on gene expression results.
Pathway Analysis, Canonical Pathways, Overlapping Pathways, Pathway Import and scoring
Pathway Analysis, Canonical Pathways, Overlapping Pathways, Pathway Import and scoring. Determine most significantly effected pathways.
Comparison Analysis
Determine most significant pathways, upstream regulators, diseases, biological functions, and more across time points, dose, or other conditions.
Network Analysis
Build and explore transcriptional networks, microRNA-mRNA target networks, phosphorylation cascades and Protein-Protein or Protein-DNA interaction networks. Identify regulatory events that lead from signaling events to transcriptional effects. Understand toxicity responses by exploring connections between drugs or targets and related genes or chemicals. edit and expand networks based on the molecular relationships most relevant to the project.
MicroRNA Target Filter
Reduce the number of steps it takes to confidently, quickly, and easily identify mRNA targets by letting you examine microRNA-mRNA pairings, explore the related biological context, and filter based on relevant biological information as well as the expression information. The microRNA Target Filter in IPA provides insights into the biological effects of microRNAs, using experimentally validated interactions from TarBase and miRecords, as well as predicted microRNA-mRNA interactions from TargetScan. Additionally, IPA includes a large number of microRNA-related findings from the peer-reviewed literature.
Tox Lists and Tox Functions
IPA-Tox uses Toxicity Functions in combination with Toxicity Lists to link experimental data to clinical pathology endpoints, understand pharmacological response, and support mechanism of action and mechanism of toxicity hypothesis generation.
Molecule Activity Predictor (MAP)
Interrogate sub-networks and Canonical Pathways and generate hypotheses by selecting a molecule of interest, indicating up or down regulation, and simulating directional consequences of downstream molecules and the inferred activity upstream in the network or pathway
Isoform View
Quickly move beyond statistical analysis of high-throughput RNA-Seq data to understand the biological implications of your data. Identify significantly regulated isoforms in your experiment and determine their potential impact using information about functional protein domains and isoform-specific literature
Gene and ChemView
IPA's Search & Explore capabilities offer researchers access to the most current Findings available on genes, drugs, chemicals, protein families, normal cellular and disease processes, and signaling and metabolic pathways.
Biomarker Filter
Rapidly identify the best biomarker candidates based on biological characteristics most relevant to the discovery study.
Path Designer
Transform your networks and pathways in IPA into publication-quality pathway graphics rich with color, customized text and fonts, biological icons, organelles, and custom backgrounds. Expand and explore pathways using the high quality content stored in IPA.
*Available for an additional cost.
Explore Our Webinars and see how the scientific community has used IPA to create novel discoveries
IPA 2013 Spring Release [48:24 minutes]
Presented by Dr. Stuart Tugendreich, Scientific Director, IPA
The 2013 IPA Spring Release is here! Powerful new functionality enables you to upload, find, and compare datasets, and understand causal connections between diseases, genes, and networks of upstream regulators. Stuart Tugendriech, PhD, Scientific Director, IPA from Ingenuity Systems gives an overview of the new IPA capabilities in the release, as well as a use case utilizing the new features and how IPA helps to Discover Causal Connections. Faster.
Ingenuity Knowledge-Based Tools for Comprehensive Interpretation of Variant & Gene Expression Data [56:16 minutes]
Presented by Jean-Noel Billaud and Megan Laurance
Ingenuity Staff Scientists Jean-Noel Billaud and Megan Laurance present strategies for integrated analysis and interpretation of variant and gene expression data generated from cell lines representative of 2
breast cancer subtypes: Claudin-Low and Luminal. These subtypes represent different disease entities associated with specific molecular alterations and histo-clinical features. Interrogating these samples at both the variant and transcript level with Ingenuity's Variant Analysis and IPA software presents a powerful approach to drawing clear molecular
paths from variants and gene expression changes to phenotypes relevant to these disease subtypes including Epithelial-to-Mesenchymal Transition and Metastasis.
A Bioinformatician's Guide to Lung Cancer: Wnt7a Signaling and Beyond [40:13 minutes]
Presented by Dr. Michael Edwards, Assistant Professor at the University of Colorado Health Sciences, Denver.
This webinar discusses an important antitumor pathway in lung cancer (Wnt7a signaling) as a framework to explain the bioinformatic analysis process using IPA. Topics covered include biological function and pathway analysis, network construction, and identifying and interpreting upstream regulators.
IPA and Coronary Artery Disease: A Case Study from Harvard [36:23 minutes]
Presented by Dr. Jochen Danny Muehlschlegel, M.D., Harvard Medical School
See how IPA was used for the discovery of novel pathways of affected genes in coronary artery disease. Cardiopulmonary bypass (CPB) with cardioplegic arrest is associated with ischemia leading to metabolic substrate depletion, reperfusion injury, apoptosis and necrosis. The study hypothesized that human left ventricular (LV) myocardium responds differently to the stress of (CPB) depending on the presence or absence of coronary artery disease (CAD). Therefore, they assessed differences in gene expression in patients undergoing aortic valve replacement (AVR) with (CPB) prior to and after cardioplegic arrest using whole-genome transcriptional profiling.
The Role of microRNAs in Kidneys of Hypertensive Patients [23:09 minutes]
Presented by Aimee Jackson, Ph.D.
MicroRNAs are small, non-coding RNAs that function as central regulators of gene expression and development. These regulatory molecules have been implicated in a wide range of normal and pathological activities, including embryonic development, cancer, inflammation, cardiovascular disease and viral infections. We explored the possibility that microRNA dysfunction in the kidney might contribute to hypertension, a significant health issue. We analyzed mRNA and microRNA expression profiling data from kidneys of untreated hypertensive patients and normotensive patients to identify microRNAs, microRNA targets, and gene networks that are dysregulated in hypertension. The results of these analyses identify microRNAs and their targets that could be biomarkers or therapeutic targets for hypertension.
Differential Expression of Focus Genes Associated Feed Efficiency [41:26 minutes]
Presented by Dr. Walter Bottje, Professor, Dept. of Poultry Science, University of Arkansas
Global RNA expression in breast muscle obtained from a male broiler line phenotyped for high or low feed efficiency (FE) was investigated using microarray analysis. By using an overlay function of IPA in which canonical pathways can be projected onto a set of genes, differentially expressed focus genes were identified. We selected 130 out of 260 possible canonical pathways in the IPA program that would likely be associated with normal metabolic activities and did not select those that were obviously tissue or disease specific. The results of this study provide additional insight into gene expression in muscle associated with the phenotypic expression of feed efficiency in broilers.
Scientific Webinar What You Should Know About Your 'Omics Data [58:11 minutes]
Presented by Tim Bonnert, PhD, Ingenuity Systems
Learn how you can now predict the cause and effect of changes in gene expression and predict the activation or inhibition of upstream molecules, such as cytokines, kinases, microRNA, receptors and many more! Included in the webinar will be an example of the biological analysis and interpretation of a gene expression data set from a study of Docetaxel Resistance in the Breast Cancer Cell Line MCF-7.
Distinct Gene Expression Profile of Regulatory T Cells in Prostate Cancer [45:00 minutes]
Presented by Simo Arredouani, Assistant Professor of Surgery at Harvard Medical School
The inhibitory role of regulatory T-cells (Tregs) in cancer is now well established. Furthermore, inhibition of Treg function has been shown both experimentally and clinically to improve the immune response towards a variety of cancers. Developing new and more effective strategies interfering with the function of Tregs in cancer requires a deep understanding of Treg suppressor machinery, and a thorough dissection of the molecular elements that orchestrate their differentiation from T cells.
A Combined Biological and Bioinformatic Analysis of Primary and Metastatic Tissues from NGS Ewing's Sarcoma Patients [58:00 minutes]
Presented by Jean-Noel Billaud, Ph.D., Ingenuity Systems and and Sylvain Foissac, Ph.D., Integromics
The Ewing's Sarcoma family of tumors is a category of cancers that predominantly affects teenagers between the ages of 10 to 20. Learn how Ingenuity Systems' IPA software and Integromics' SeqSolve software were used to investigate Ewing's Sarcoma patient samples generated from Helicos' NGS technology. We will present a combined bioinformatic and biological analysis of Ewing's Sarcoma patient samples, focusing on the differences between primary and metastatic tissues. IPA was used to analyze the significantly regulated genes and Integromics' NGS SeqSolve software was used to prepare the RNA-Seq data. IPA's new transcription factor analysis tool and downstream effects map were used to help narrow down targets and visualize the biological networks.
Using IPA to Analyze Illumina RNA-Seq Data Reveals Abundance-Specific Biological Signatures in Alzheimer's Disease [33:44 minutes]
Presented by Darryl Gietzen, Ph.D., Ingenuity Systems
This webinar discusses how IPA was used to interpret Alzheimer's disease biology by comparing Illumina RNA-Seq data from Alzheimer's disease (AD) and normal brain samples. This analysis revealed very specific biological changes in certain classes of transcript expression, demonstrating how the unique benefits of RNA-Seq can help characterize disease changes.
A diverse group of researchers are using IPA to understand and interpret complex biological systems. Meet a few and learn more about how they are using IPA.
"I'm excited to leverage the new Molecular Activity Predictor (MAP) and Causal Network Analysis in Ingenuity's IPA. The powerful analytic capability for insilico data prediction to infer upstream activity in the network or pathway in IPA allows me to go beyond my own knowledge to further understand the biology."
Anirban P. Mitra, M.D., Ph.D., Senior Research Associate, University of Southern California.

"In our study, we coupled analysis with Ingenuity's IPA and microarray data to evaluate the impact of exercise and muscle aging by measuring the variation in the products being made. The analysis determined that the genetic regulators of age-related genes were distinct and unrelated to the regulators of exercise-influenced genes. Using IPA, we were able to capture the relevant networks more easily and with far less cost than traditional methods."
Dr. James A. Timmons, Loughborough University, United Kingdom

"We've recently seen that genes associated with critical cellular functions are often regulated post-transcriptionally. Ingenuity's Upstream Regulator in IPA allows for the identification of these important regulators from expression data sets and is going to completely change the field of bioinformatics by identifying these potential regulators and not limiting the analysis to just the transcriptome."
Michael Edwards, Ph.D., Assistant Professor, UC Denver
