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Step by step guide

Start with Biomedical Genomics Workbench

  1. Upload RNA-seq data (FASTQ files)
  2. Align to the genome of interest (human Ensembl or RefSeq)
  3. Quantitate and obtain differential expression between samples

Seamlessly send data from Biomedical Genomics Workbench to IPA

  1. Visualize the differentially expressed genes and spliced transcripts
  2. Understand which signaling pathways are involved
  3. Discover potential transcriptional program(s) that are induced or suppressed
  4. Discover specific biological processes contributing to a specific disease or state
  5. Highlight new hypotheses