read.fasta: Read FASTA formated Sequences

In bio3d: Biological Structure Analysis

Read FASTA formated Sequences

Description

Read aligned or un-aligned sequences from a FASTA format file.

Usage

read.fasta(file, rm.dup = TRUE, to.upper = FALSE, to.dash=TRUE)

Arguments

file	input sequence file.
rm.dup	logical, if TRUE duplicate sequences (with the same names/ids) will be removed.
to.upper	logical, if TRUE residues are forced to uppercase.
to.dash	logical, if TRUE ‘.’ gap characters are converted to ‘-’ gap characters.

Value

A list with two components:

ali	an alignment character matrix with a row per sequence and a column per equivalent aminoacid/nucleotide.
ids	sequence names as identifers.
call	the matched call.

Note

For a description of FASTA format see: https://www.ncbi.nlm.nih.gov/BLAST/blastcgihelp.shtml. When reading alignment files, the dash ‘-’ is interpreted as the gap character.

Author(s)

Barry Grant

References

Grant, B.J. et al. (2006) Bioinformatics 22, 2695–2696.

See Also

read.fasta.pdb

Examples

# Read alignment
aln <- read.fasta(system.file("examples/hivp_xray.fa",package="bio3d"))

# Print alignment overview
aln

# Sequence names/ids
head( aln$id )

# Alignment positions 335 to 339
head( aln$ali[,33:39] )

# Sequence d2a4f_b
aa123( aln$ali["d2a4f_b",] )

# Write out positions 33 to 45 only
#aln$ali=aln$ali[,30:45]
#write.fasta(aln, file="eg2.fa")

bio3d documentation built on Oct. 30, 2024, 1:08 a.m.