View source: R/feature_file_editor.R
feature_file_editor | R Documentation |
A wrapper function that executes all prediction steps for each strand and builds the final GFF3 annotation.
feature_file_editor(
bam_directory = ".",
bam_list = "",
original_annotation_file,
annot_file_dir = ".",
output_file,
original_sRNA_annotation,
low_coverage_cutoff,
high_coverage_cutoff,
min_sRNA_length,
min_UTR_length,
paired_end_data = FALSE,
strandedness = "stranded"
)
bam_directory |
The directory containing BAM files. |
bam_list |
Optional newline separated text file of filenames of bam files. File must be located in bam_location directory. |
original_annotation_file |
GFF3 genome annotation file. |
annot_file_dir |
The directory containing the GFF3 annotation file. |
output_file |
A string containing the name of an output file. |
original_sRNA_annotation |
A string indicating how the biotype of pre-annotated ncRNA, which can be found in the attribute column.In case if the user does not know how the sRNA is annotated, it can be set as "unknown". In this case, all RNAs apart from tRNAs and rRNAs will be removed from the selection. |
low_coverage_cutoff |
An integer indicating the low coverage threshold value. |
high_coverage_cutoff |
An integer indicating the high coverage threshold value. |
min_sRNA_length |
An integer indicating the minimum peak width/sRNA length. |
min_UTR_length |
An integer indicating the minimum UTR length. |
paired_end_data |
A boolean indicating if the reads are paired-end. |
strandedness |
A string outlining the type of the sequencing library: stranded, or reversely stranded. |
Outputs a new GFF3 file populated with predicted sRNAs and UTRs.
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