read.fasta {phylotools} | R Documentation |
Read FASTA file
Description
Read and convert the fasta file to data frame
Usage
read.fasta(file = NULL, clean_name = FALSE)
Arguments
file |
character string representing the name of the fasta file. |
clean_name |
logical, representing cleaning of the names will be performed. Punctuation characters and white space be replaced by "_" . See |
Details
In this function, names of the sequences are identified by ">", and all the lines before next ">" will be concatenated.
Value
a data frame with two columns: (1) seq.name, the names for all the sequences. (2) seq.text, the raw sequence data.
Note
Punctuation characters and white space in the names of the sequences will be replaced by "_".
Author(s)
Jinlong Zhang <jinlongzhang01@gmail.com>
References
http://www.genomatix.de/online_help/help/sequence_formats.html
See Also
read.phylip
,dat2fasta
,dat2phylip
,split_dat
Examples
cat(
">seq_2", "GTCTTATAAGAAAGAATAAGAAAG--AAATACAAA-------AAAAAAGA",
">seq_3", "GTCTTATAAGAAAGAAATAGAAAAGTAAAAAAAAA-------AAAAAAAG",
">seq_5", "GACATAAGACATAAAATAGAATACTCAATCAGAAACCAACCCATAAAAAC",
">seq_8", "ATTCCAAAATAAAATACAAAAAGAAAAAACTAGAAAGTTTTTTTTCTTTG",
">seq_9", "ATTCTTTGTTCTTTTTTTTCTTTAATCTTTAAATAAACCTTTTTTTTTTA",
file = "trn1.fasta", sep = "\n")
res <- read.fasta("trn1.fasta")
unlink("trn1.fasta")
[Package phylotools version 0.2.2 Index]