View source: R/align_based_quan.R
| align_based_quan | R Documentation | 
alignment-based workflow
align_based_quan( pair, taxa, genome, annotation, novel_transcript = FALSE, threads = 4, hisat2_build_add = NULL, hisat2_add = NULL, stringtie_add = NULL )
| pair | 'single' for single-end (SE) or 'paired' for paired-end (PE) reads. | 
| taxa | the scientific or common name of the organism. | 
| genome | the reference genome. | 
| annotation | the annotation file. | 
| novel_transcript | logic, whether identifying novel transcripts is expected or not. Default is FALSE. | 
| threads | the number of threads to be used. Default is 4. | 
| hisat2_build_add | additional parameters to customize hisat2 build command. Default is NULL. | 
| hisat2_add | additional parameters to customize hisat2 command. Default is NULL. | 
| stringtie_add | additional parameters to customize stringtie command. Default is NULL. | 
None
## Not run: 
test_Homo_sapiens.fna <- system.file('extdata', 'test_Homo_sapiens.fna', package = 'BP4RNAseq')
test_Homo_sapiens.gff <- system.file('extdata', 'test_Homo_sapiens.gff', package = 'BP4RNAseq')
align_based_quan(pair = 'paired', taxa = 'Homo sapiens', 
genome = test_Homo_sapiens.fna, 
annotation = test_Homo_sapiens.gff, novel_transcript = FALSE)
## End(Not run)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.