DNAbin | R Documentation |
These functions help to manipulate DNA sequences coded in the bit-level coding scheme.
## S3 method for class 'DNAbin'
print(x, printlen = 6, digits = 3, ...)
## S3 method for class 'DNAbin'
rbind(...)
## S3 method for class 'DNAbin'
cbind(..., check.names = TRUE, fill.with.gaps = FALSE,
quiet = FALSE)
## S3 method for class 'DNAbin'
x[i, j, drop = FALSE]
## S3 method for class 'DNAbin'
as.matrix(x, ...)
## S3 method for class 'DNAbin'
c(..., recursive = FALSE)
## S3 method for class 'DNAbin'
as.list(x, ...)
## S3 method for class 'DNAbin'
labels(object, ...)
x , object |
an object of class |
... |
either further arguments to be passed to or from other
methods in the case of |
printlen |
the number of labels to print (6 by default). |
digits |
the number of digits to print (3 by default). |
check.names |
a logical specifying whether to check the rownames before binding the columns (see details). |
fill.with.gaps |
a logical indicating whether to keep all
possible individuals as indicating by the rownames, and eventually
filling the missing data with insertion gaps (ignored if
|
quiet |
a logical to switch off warning messages when some rows are dropped. |
i , j |
indices of the rows and/or columns to select or to drop. They may be numeric, logical, or character (in the same way than for standard R objects). |
drop |
logical; if |
recursive |
for compatibility with the generic (unused). |
These are all ‘methods’ of generic functions which are here applied to
DNA sequences stored as objects of class "DNAbin"
. They are
used in the same way than the standard R functions to manipulate
vectors, matrices, and lists. Additionally, the operators [[
and $
may be used to extract a vector from a list. Note that
the default of drop
is not the same than the generic operator:
this is to avoid dropping rownames when selecting a single sequence.
These functions are provided to manipulate easily DNA sequences coded with the bit-level coding scheme. The latter allows much faster comparisons of sequences, as well as storing them in less memory compared to the format used before ape 1.10.
For cbind
, the default behaviour is to keep only individuals
(as indicated by the rownames) for which there are no missing data. If
fill.with.gaps = TRUE
, a ‘complete’ matrix is returned,
enventually with insertion gaps as missing data. If check.names
= TRUE
(the default), the rownames of each matrix are checked, and
the rows are reordered if necessary (if some rownames are duplicated,
an error is returned). If check.names = FALSE
, the matrices
must all have the same number of rows, and are simply binded; the
rownames of the first matrix are used. See the examples.
as.matrix
may be used to convert DNA sequences (of the same
length) stored in a list into a matrix while keeping the names and the
class. as.list
does the reverse operation.
an object of class "DNAbin"
in the case of rbind
,
cbind
, and [
.
Emmanuel Paradis
Paradis, E. (2007) A Bit-Level Coding Scheme for Nucleotides. https://emmanuelparadis.github.io/misc/BitLevelCodingScheme_20April2007.pdf
Paradis, E. (2012) Analysis of Phylogenetics and Evolution with R (Second Edition). New York: Springer.
as.DNAbin
, read.dna
,
read.GenBank
, write.dna
,
image.DNAbin
,AAbin
The corresponding generic functions are documented in the package base.
data(woodmouse)
woodmouse
print(woodmouse, 15, 6)
print(woodmouse[1:5, 1:300], 15, 6)
### Just to show how distances could be influenced by sampling:
dist.dna(woodmouse[1:2, ])
dist.dna(woodmouse[1:3, ])
### cbind and its options:
x <- woodmouse[1:2, 1:5]
y <- woodmouse[2:4, 6:10]
as.character(cbind(x, y)) # gives warning
as.character(cbind(x, y, fill.with.gaps = TRUE))
## Not run:
as.character(cbind(x, y, check.names = FALSE)) # gives an error
## End(Not run)
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