View source: R/count_features.R
count_features | R Documentation |
This is a function to employ Rsubread featureCounts to quantify expression of annotated and predicted elements
count_features(
bam_dir = ".",
annotation_dir = ".",
annotation_file,
output_dir = ".",
output_filename = "dataset",
chromosome_alias_file,
strandedness,
is_paired_end,
excl_rna = T,
...
)
bam_dir |
The directory where bam files located |
annotation_dir |
The directory where annotation file is located |
annotation_file |
The complete annotation file: GFF3 or GTF genome annotation file |
output_dir |
The full directory path for CSV output files to be written |
output_filename |
The name for the output files–for example dataset name |
chromosome_alias_file |
A comma-delimited TXT file containing a character string with the chromosome names. This file has to have two columns: first with the chromosome name in the annotation file, second with the chromosome name in the BAM file. |
strandedness |
A string outlining the type of the sequencing library: unstranded, stranded, or reversely stranded. |
is_paired_end |
A boolean indicating if the reads are paired-end. |
excl_rna |
A boolean indicating if misc RNA features (rRNA, tRNA) are excluded from quantification. (Defaults=T) |
... |
Optional parameters passed on to featureCounts() Default: allowMultiOverlap = T, fraction = T |
Count tables for each feature are written into separate files, as well as the result summary.
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