bt.getfasta | R Documentation |
Extract DNA sequences from a fasta file based on feature coordinates.
bt.getfasta(
fi,
bed,
fo = NULL,
name = NULL,
nameplus = NULL,
nameOnly = NULL,
split = NULL,
tab = NULL,
bedOut = NULL,
s = NULL,
fullHeader = NULL,
rna = NULL,
output = NULL
)
fi |
<fasta> |
bed |
<bed/gff/vcf> |
fo |
Output file (opt., default is STDOUT |
name |
Use the name field and coordinates for the FASTA header |
nameplus |
(deprecated) Use the name field and coordinates for the FASTA header |
nameOnly |
Use the name field for the FASTA header |
split |
Given BED12 fmt., extract and concatenate the sequences from the BED "blocks" (e.g., exons) |
tab |
Write output in TAB delimited format. |
bedOut |
Report extract sequences in a tab-delimited BED format instead of in FASTA format. - Default is FASTA format. |
s |
Force strandedness. If the feature occupies the antisense, strand, the sequence will be reverse complemented. - By default, strand information is ignored. |
fullHeader |
Use full fasta header. - By default, only the word before the first space or tab is used. |
rna |
The FASTA is RNA not DNA. Reverse complementation handled accordingly. |
output |
Output filepath instead of returning output in R. |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.