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·         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

·         Find genes that are alternatively spliced among phenotypes

·         Set up a basic analysis of variance (ANOVA) model

·         Detect nucleotide variations across samples or comparing to reference genome·         Find nonannotated regions and map it to the genome

Note: the workflow described below is enabled in Partek Genomics Suite version 7.0 software. Please fill out the form at www.partek.com/PartekSupport to request this version or use the Help > Check for Updates command to check whether you have the latest released version. The screenshots shown within this tutorial may vary across platforms and across different versions of Partek Genomics Suite.

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