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RNA-Seq is a high-throughput sequencing technology used to generate information about a sample’s RNA content. Partek® Genomics Suite® offers convenient visualization and analysis of the high volumes of data generated by RNA-Seq experiments.
This tutorial will illustrate illustrates how to:
- Import large next-gen data sets
- Add attribute data to your files
- Visualize large next-gen data sets
- Obtain read counts for each of the transcripts in a database
- Find transcripts that are differentially expressed among phenotypes
- Visualize differential expression of isoforms among phenotypes
- Find genes that are alternatively spliced among phenotypes
- Find nonannotated regions and map it to the genome
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