Package 'agvgd' reference manual

Title:	An R Implementation of the 'Align-GVGD' Method
Description:	'Align-GVGD' ('A-GVGD') is a method to predict the impact of 'missense' substitutions based on the properties of amino acid side chains and protein multiple sequence alignments <doi:10.1136/jmg.2005.033878>. 'A-GVGD' is an extension of the original 'Grantham' distance to multiple sequence alignments. This package provides an alternative R implementation to the web version found on <http://agvgd.hci.utah.edu/>.
Authors:	Ramiro Magno [aut, cre] , Isabel Duarte [aut] , Ana-Teresa Maia [aut] , CINTESIS [cph, fnd]
Maintainer:	Ramiro Magno <[email protected]>
License:	MIT + file LICENSE
Version:	0.1.2
Built:	2024-11-12 04:41:29 UTC
Source:	https://github.com/maialab/agvgd

Align-GVGD (A-GVGD)

Description

This function implements the Align-GVGD (A-GVGD) method described in Tavtigian et al. (2006).

A-GVGD combines multiple sequence alignment of orthologous sequences with the Grantham distance to classify missense variants, i.e. to distinguish human disease susceptibility missense changes from changes of little clinical significance.

The biochemical variation at each alignment position is converted to a Grantham Variation score (GV) and the difference between these properties and those of the variant amino acid being assessed are calculated and a Grantham Difference score generated (GD). The predicted effect is classed as C0, C15, C25, C35, C45, C55, or C65, with C65 most likely to interfere with function and C0 least likely.

Usage

agvgd(
  alignment,
  poi,
  sub,
  mode = c("recycle", "expand_grid"),
  sort = FALSE,
  keep_self = TRUE,
  digits = 2L
)
agvgd(
  alignment,
  poi,
  sub,
  mode = c("recycle", "expand_grid"),
  sort = FALSE,
  keep_self = TRUE,
  digits = 2L
)

Arguments

`alignment`	A character matrix or an alignment object obtained with `read_alignment()`. Rows are expected to be sequences of single characters (protein residues), and columns the alignment positions. The first row must be the reference sequence, i.e. the sequence whose substitutions will be evaluated against.
`poi`	A whole number indicating the position of interest (POI).
`sub`	A character vector of protein residue substitutions to be classified. The amino acids must be provided as one-letter symbols.
`mode`	If both `poi` and `sub` contain more than one element, `mode` specifies how these two inputs are combined. If `mode = 'recycle'` the shortest vector is recycled to match the length of the longest. If `mode = 'expand_grid'`, all combinations between elements of `poi` and `sub` are combined.
`sort`	Whether to sort the output by `gd`, or not. Default is `FALSE`.
`keep_self`	Whether to keep those results in the output that correspond to residues being the same in `ref` and `sub`. Default is `TRUE`. But it will be useful to change it to `FALSE` if want to compare the results with those provided by http://agvgd.hci.utah.edu/ that filters them out.
`digits`	Integer indicating the number of decimal places to be used in rounding `gv` and `gd` values. Default is `2`. Note that the calculation of the `prediction` variable won't be affected by rounding of `gv` and `gd`, as it is calculated prior to the rounding.

Value

A tibble whose observations refer to the combination alignment position and amino acid substitution; consists of seven variables:

res: Position of the amino acid residue in the reference protein (first sequence in the alignment). This position corresponds to poi minus the gaps in the alignment.
poi: Position of interest, i.e. the alignment position at which the amino acid substitution is being assessed.
ref: Reference amino acid, i.e. the amino acid in the first sequence of the alignment, at the position of interest.
sub: Amino acid substitution being assessed.
gv: Grantham variation score.
gd: Grantham difference score.
prediction: Predicted effect of the amino acid substitution. This is classed as C0, C15, C25, C35, C45, C55, or C65, with C65 most likely to interfere with function and C0 least likely.

References

Tavtigian, S.V., Deffenbaugh, A. M., Yin, L., Judkins, T., Scholl, T., Samollow, P.B., de Silva, D., Zharkikh, A., Thomas, A. Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral. Journal of Medical Genetics 43, 295–305 (2006). doi:10.1136/jmg.2005.033878.
Mathe, E., Olivier, M., Kato, S., Ishioka, C., Hainaut, P., Tavtigian, S.V. Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods. Nucleic Acids Research 34, 1317–1325 (2006). doi:10.1093/nar/gkj518.

Examples

# Read an alignment into R, e.g. the alignment for gene ATM.
alignment_ATM <- read_alignment(gene = 'ATM')

# Predict the impact of changing the first residue (Met) to a Serine (S).
agvgd(alignment = alignment_ATM, poi = 1, sub = 'S')

# `poi` can be a vector of positions, e.g., 3 thru 10, allow for prediction
# of multiple positions at once.
agvgd(alignment = alignment_ATM, poi = 3:10, sub = 'S')

# `poi` expects a position in the frame of reference of the alignment, i.e.
# an alignment position (a column index). However, if you know instead
# the residue position in the reference sequence (first sequence in the
# alignment), then you may use the function `res_to_poi()`
# to convert from residue position to alignment position.
#
# Example: The second residue in the reference sequence of the ATM alignment
# is a Serine, after a Methionine. In the alignment, there is a gap between
# the two residues, so the alignment is 3 but the residue position on the
# protein is 2.
(poi2 <- res_to_poi(alignment_ATM, 2))
agvgd(alignment = alignment_ATM, poi = poi2, sub = 'A')

# Because changes are context-dependent, i.e. they depend on the residue
# variation observed at a given alignment position, the same reference
# residue when replaced with the same substitution will in general have
# a different predicted impact.
agvgd(alignment = alignment_ATM, poi = 9:10, sub = 'S')

# Use the ancillary function `amino_acids()` to get a vector of one-letter
# residue substitutions if you want to quickly assess the impact of all
# possible substitutions.
agvgd(alignment = alignment_ATM, poi = 1, sub = amino_acids())

# Parameter `mode` gives you flexibility on how to combine `poi` and `sub`.
agvgd(alignment = alignment_ATM, poi = 3:4, sub = c('A', 'V'))

# Use 'expand_grid' for all combinations.
agvgd(alignment = alignment_ATM, poi = 3:4, sub = c('A', 'V'), mode = 'expand_grid')

# Read an alignment into R, e.g. the alignment for gene ATM.
alignment_ATM <- read_alignment(gene = 'ATM')

# Predict the impact of changing the first residue (Met) to a Serine (S).
agvgd(alignment = alignment_ATM, poi = 1, sub = 'S')

# `poi` can be a vector of positions, e.g., 3 thru 10, allow for prediction
# of multiple positions at once.
agvgd(alignment = alignment_ATM, poi = 3:10, sub = 'S')

# `poi` expects a position in the frame of reference of the alignment, i.e.
# an alignment position (a column index). However, if you know instead
# the residue position in the reference sequence (first sequence in the
# alignment), then you may use the function `res_to_poi()`
# to convert from residue position to alignment position.
#
# Example: The second residue in the reference sequence of the ATM alignment
# is a Serine, after a Methionine. In the alignment, there is a gap between
# the two residues, so the alignment is 3 but the residue position on the
# protein is 2.
(poi2 <- res_to_poi(alignment_ATM, 2))
agvgd(alignment = alignment_ATM, poi = poi2, sub = 'A')

# Because changes are context-dependent, i.e. they depend on the residue
# variation observed at a given alignment position, the same reference
# residue when replaced with the same substitution will in general have
# a different predicted impact.
agvgd(alignment = alignment_ATM, poi = 9:10, sub = 'S')

# Use the ancillary function `amino_acids()` to get a vector of one-letter
# residue substitutions if you want to quickly assess the impact of all
# possible substitutions.
agvgd(alignment = alignment_ATM, poi = 1, sub = amino_acids())

# Parameter `mode` gives you flexibility on how to combine `poi` and `sub`.
agvgd(alignment = alignment_ATM, poi = 3:4, sub = c('A', 'V'))

# Use 'expand_grid' for all combinations.
agvgd(alignment = alignment_ATM, poi = 3:4, sub = c('A', 'V'), mode = 'expand_grid')

Pre-bundled alignments

Description

This function returns either a data frame of the pre-bundled alignments if parameter gene is missing (default behaviour), or the file name of the alignment of a supplied gene name.

Usage

alignment_file(gene)
alignment_file(gene)

Arguments

gene

The gene name of one of the pre-bundled alignments. Run alignment_file() to list all genes available.

Value

Either a data frame of the pre-bundled alignments if parameter gene is missing (default behaviour), or the file name of the alignment of a supplied gene name.

Examples

# List pre-bundled alignment file names and associated genes
alignment_file()

# Retrieve the file name of an alignment
alignment_file("BRCA1")

# You may get the full path to an alignment file with `system.file()`
system.file("extdata", alignment_file("BRCA1"), package = "agvgd")

# List pre-bundled alignment file names and associated genes
alignment_file()

# Retrieve the file name of an alignment
alignment_file("BRCA1")

# You may get the full path to an alignment file with `system.file()`
system.file("extdata", alignment_file("BRCA1"), package = "agvgd")

The 20 standard amino acids

Description

The 20 amino acids that are encoded directly by the codons of the universal genetic code.

Usage

amino_acids(code = c("one_letter", "three_letter"))
amino_acids(code = c("one_letter", "three_letter"))

Arguments

code

The type of amino acid symbol to be returned, one-letter ('one_letter') or three-letter ('three_letter') codes.

Value

A character vector of the 20 standard amino acids.

Examples

# By default `amino_acids` returns one-letter symbols
amino_acids()

# Use code = 'three_letter' instead for three-letter symbols
amino_acids(code = 'three_letter')

# By default `amino_acids` returns one-letter symbols
amino_acids()

# Use code = 'three_letter' instead for three-letter symbols
amino_acids(code = 'three_letter')

Determine CPV ranges

Description

This function determines the range (minimum and maximum) values for the three amino acid side chain property values — composition, polarity and molecular volume — from the amino acids at the alignment position of interest.

The alignment passed in alignment must be an already focused alignment of three columns whose second column is the position of interest.

Usage

cpv_ranges(alignment, exclude = c("-", "X", NA_character_))
cpv_ranges(alignment, exclude = c("-", "X", NA_character_))

Arguments

`alignment`	A character matrix or an alignment object obtained with `read_alignment()`. Rows are expected to be sequences of single characters (protein residues), and columns the alignment positions. The first row must be the reference sequence, i.e. the sequence whose substitutions will be evaluated against.
`exclude`	A vector of character values to be ignored when collecting the amino acids at the position of interest.

Value

A tibble with one single row, of six variables, i.e., the minimum and maximum values for composition (c_min and c_max), polarity (p_min and p_max) and molecular volume (v_min and v_max).

Examples

# You need to first focus the alignment around the position of interest. The
# position of interest is position 4 in the example below. After subsetting
# the alignment, it becomes position 2.
alignment <- read_alignment('ATM')

alignment[, 3:5]

cpv_ranges(alignment[, 3:5])

# If at the position of interest there are symbols other than amino acid
# symbols, e.g. gaps ("-"), then these are ignored and the calculated ranges
# are based only on the observed amino acids.
alignment[, 270:272]

cpv_ranges(alignment[, 270:272])

# You need to first focus the alignment around the position of interest. The
# position of interest is position 4 in the example below. After subsetting
# the alignment, it becomes position 2.
alignment <- read_alignment('ATM')

alignment[, 3:5]

cpv_ranges(alignment[, 3:5])

# If at the position of interest there are symbols other than amino acid
# symbols, e.g. gaps ("-"), then these are ignored and the calculated ranges
# are based only on the observed amino acids.
alignment[, 270:272]

cpv_ranges(alignment[, 270:272])

Deviation function

Description

This function calculates the deviation in the sense of the Grantham deviation as introduced by Tavtigian et al. (2006). Essentially, if x lies within the range [min, max], then dev() returns 0. If x is either below min, or above max, then dev() returns the absolute difference between x and min or max, respectively.

dev definition

Inputs are recycled in the sense of vctrs::vec_recycle().

Usage

dev(x, min, max)
dev(x, min, max)

Arguments

`x`	A numeric vector.
`min`	A numeric vector.
`max`	A numeric vector.

Details

Here's a plot showcasing dev() with min = -4 and max = 3:

x <- -10:10; min <- -4; max <- 3
plot(x, y = dev(x, min, max), type = 'l', xlab = 'x', ylab = 'deviation')

Value

A numeric vector of deviations.

Examples

# `dev()` returns absolute differences from either min or max (whichever is
# closest).
dev(10, min = -4, max = 4)
dev(-10, min = -4, max = 4)

# `x` can be a vector
dev(-10:10, min = -4, max = 4)

# `min` and `max` can also be vectors, they will be recycled
dev(-10:10, min = -4:16, max = 4:24)

# If `x` contains `NA` values, then `dev()` will return `NA` for
# those cases
dev(c(10, NA), min = -4, max = 4)

# For each calculation of deviation, only either `min` or `max` is used. If
# the unused parameter is `NA` it won't affect the calculation:
dev(c(10, 3), min = c(NA, -4), max = 4)
dev(c(10, -5), min = -4, max = c(4, NA))

# `dev()` returns absolute differences from either min or max (whichever is
# closest).
dev(10, min = -4, max = 4)
dev(-10, min = -4, max = 4)

# `x` can be a vector
dev(-10:10, min = -4, max = 4)

# `min` and `max` can also be vectors, they will be recycled
dev(-10:10, min = -4:16, max = 4:24)

# If `x` contains `NA` values, then `dev()` will return `NA` for
# those cases
dev(c(10, NA), min = -4, max = 4)

# For each calculation of deviation, only either `min` or `max` is used. If
# the unused parameter is `NA` it won't affect the calculation:
dev(c(10, 3), min = c(NA, -4), max = 4)
dev(c(10, -5), min = -4, max = c(4, NA))

Grantham deviation

Description

This function calculates the Grantham deviation ( $\mathrm{gd}$ ):

$\mathrm{gd} = \rho \left((\alpha\ \mathrm{dev}^2(c_x, c_{min}, c_{max}) + \beta\ \mathrm{dev}^2(p_x, p_{min}, p_{max}) + \gamma\ \mathrm{dev}^2(v_x, v_{min}, v_{max})\right)^\frac{1}{2}$

where $c_x$ is the value for composition $c$ of amino acid $x$ , i.e. the atomic weight ratio of hetero (noncarbon) elements in end groups or rings to carbons in the side chain; $p_x$ is the value for polarity $p$ of amino acid $x$ ; and, $v_x$ is the value for molecular volume $v$ of amino acid $x$ .

$c_x$ , $p_x$ and $v_x$ are looked up in grantham::amino_acids_properties based on the amino acid identities passed in x. The function $\mathrm{dev}$ is implemented in dev(). Remaining variables in the equation are arguments to gd() and hence are explained below in the Arguments section.

Usage

gd(
  x,
  c_min,
  c_max,
  p_min,
  p_max,
  v_min,
  v_max,
  alpha = 1.833,
  beta = 0.1018,
  gamma = 0.000399,
  rho = 50.723
)
gd(
  x,
  c_min,
  c_max,
  p_min,
  p_max,
  v_min,
  v_max,
  alpha = 1.833,
  beta = 0.1018,
  gamma = 0.000399,
  rho = 50.723
)

Arguments

`x`	A character vector of one-letter amino acid codes, indicating missense substitutions.
`c_min`	Amino acid composition, minimum value.
`c_max`	Amino acid, composition, maximum value.
`p_min`	Amino acid polarity, minimum value.
`p_max`	Amino acid polarity, maximum value.
`v_min`	Amino acid molecular volume, maximum value.
`v_max`	Amino acid molecular volume, maximum value.
`alpha`	The constant $\alpha$ in Grantham's equation. It is the square inverse of the mean of the composition property.
`beta`	The constant $\beta$ in Grantham's equation. It is the square inverse of the mean of the polarity property.
`gamma`	The constant $\gamma$ in Grantham's equation. It is the square inverse of the mean of the molecular volume property.
`rho`	Grantham's distances reported in Table 2, Science (1974). 185(4154): 862–4 by R. Grantham, are scaled by a factor (here named $\rho$ ) such that the mean value of all distances are 100. The `rho` parameter allows this factor $\rho$ to be changed. By default $\rho=50.723$ , the same value used by Grantham. This value is originally mentioned in the caption of Table 2 of the aforementioned paper.

Value

A numeric vector of Grantham deviations. Each deviation corresponds to one of the amino acids indicated in x.

Examples

gd('S', c_min = 0.39, c_max = 0.74, p_min =4.9, p_max =8.6, v_min = 3, v_max = 32.5)

gd('S', c_min = 0.39, c_max = 0.74, p_min =4.9, p_max =8.6, v_min = 3, v_max = 32.5)

Grantham variation

Description

This function calculates the Grantham variation ( $\mathrm{gv}$ ):

$\mathrm{gv} = \rho \left((\alpha (c_{max}-c_{min})^2 + \beta (p_{max}-p_{min})^2 + \gamma (v_{max}-v_{min})^2\right)^\frac{1}{2}$

The minimum and maximum values are those observed for a set of amino acid residues at the alignment position of interest.

Usage

gv(
  c_min,
  c_max,
  p_min,
  p_max,
  v_min,
  v_max,
  alpha = 1.833,
  beta = 0.1018,
  gamma = 0.000399,
  rho = 50.723
)
gv(
  c_min,
  c_max,
  p_min,
  p_max,
  v_min,
  v_max,
  alpha = 1.833,
  beta = 0.1018,
  gamma = 0.000399,
  rho = 50.723
)

Arguments

`c_min`	Amino acid composition, minimum value.
`c_max`	Amino acid, composition, maximum value.
`p_min`	Amino acid polarity, minimum value.
`p_max`	Amino acid polarity, maximum value.
`v_min`	Amino acid molecular volume, maximum value.
`v_max`	Amino acid molecular volume, maximum value.
`alpha`	The constant $\alpha$ in Grantham's equation. It is the square inverse of the mean of the composition property.
`beta`	The constant $\beta$ in Grantham's equation. It is the square inverse of the mean of the polarity property.
`gamma`	The constant $\gamma$ in Grantham's equation. It is the square inverse of the mean of the molecular volume property.
`rho`	Grantham's distances reported in Table 2, Science (1974). 185(4154): 862–4 by R. Grantham, are scaled by a factor (here named $\rho$ ) such that the mean value of all distances are 100. The `rho` parameter allows this factor $\rho$ to be changed. By default $\rho=50.723$ , the same value used by Grantham. This value is originally mentioned in the caption of Table 2 of the aforementioned paper.

Value

A numeric vector of grantham variation values.

Examples

# Example based on values from Figure 1C of Tavtigian et al. (2006),
# https://doi.org/10.1136/jmg.2005.033878.
gv(c_min = 0, c_max = 0, p_min = 5.7, p_max = 4.9, v_min = 132, v_max = 105)

# Example based on values from Figure 1C of Tavtigian et al. (2006),
# https://doi.org/10.1136/jmg.2005.033878.
gv(c_min = 0, c_max = 0, p_min = 5.7, p_max = 4.9, v_min = 132, v_max = 105)

Convert an alignment position to residue position

Description

This function converts an alignment position to a position in the frame of the reference protein sequence, i.e., to the positions of the amino acids in the first sequence of the alignment.

Usage

poi_to_res(alignment, poi)
poi_to_res(alignment, poi)

Arguments

`alignment`	An alignment.
`poi`	An alignment position.

Value

An integer vector of positions of the amino acid residues in the reference sequence.

Examples

align_ATM <- read_alignment('ATM')
align_ATM[, 1:5]

# Convert the positions of the first five alignment positions to residue positions
poi_to_res(align_ATM, 1:5)

align_ATM <- read_alignment('ATM')
align_ATM[, 1:5]

# Convert the positions of the first five alignment positions to residue positions
poi_to_res(align_ATM, 1:5)

Converts a sequence profile to an alignment

Description

This function converts a sequence profile as provided in the format of the package {protean} to an {agvgd} alignment — an alignment in this sense is simply a character matrix whose elements are protein residues in one-letter notation, rows are sequences and columns correspond to alignment positions.

Usage

profile_to_alignment(profile)
profile_to_alignment(profile)

Arguments

profile

A sequence profile object as returned by protean::read_profile() or protean::get_profile(). See the {protean} package at https://github.com/maialab/protean.

Value

An alignment object, i.e. a character matrix whose elements are protein residues in one-letter notation. Rows are sequences and columns are alignment positions.

Read a protein sequence multiple alignment

Description

Reads a protein sequence multiple alignment (PSMA) from either a set of pre-bundled alignments, by gene name, or from a Multi-FASTA file.

Usage

read_alignment(
  gene = c("ATM", "BRCA1", "BRCA2", "CHEK2", "MRE11", "MSH6", "NBN", "PALB2", "PMS2",
    "RAD50", "RAD51", "XRCC2"),
  file = NULL
)
read_alignment(
  gene = c("ATM", "BRCA1", "BRCA2", "CHEK2", "MRE11", "MSH6", "NBN", "PALB2", "PMS2",
    "RAD50", "RAD51", "XRCC2"),
  file = NULL
)

Arguments

`gene`	The gene name for which an alignment is provided with this package. Use the function `alignment_file()` to list the pre-bundled alignments.
`file`	The path to a Multi-FASTA file. If this argument is given, it takes precedence over the `gene` parameter.

Value

An alignment object; essentially, a character matrix, whose elements are protein residues in one-letter notation. Rows are sequences and columns are alignment positions.

Examples

# Read in the alignment for the gene XRCC2
read_alignment('XRCC2')

# Also read in the alignment for the gene XRCC2, but now by specifying
# directly the path to the file.
path <- system.file("extdata", alignment_file("XRCC2"), package = "agvgd")
read_alignment(file = path)

# Read in the alignment for the gene XRCC2
read_alignment('XRCC2')

# Also read in the alignment for the gene XRCC2, but now by specifying
# directly the path to the file.
path <- system.file("extdata", alignment_file("XRCC2"), package = "agvgd")
read_alignment(file = path)

Read a file with amino acid substitutions

Description

This function reads a file with amino acid substitutions. The format of should be the same one as requested by the web version of Align-GVGD.

Usage

read_substitutions(
  file = stop("`file` must be specified"),
  amino_acid_code = c("one_letter", "three_letter")
)
read_substitutions(
  file = stop("`file` must be specified"),
  amino_acid_code = c("one_letter", "three_letter")
)

Arguments

`file`	The path to a file with amino acid substitutions.
`amino_acid_code`	The type of symbol used for amino acids in the returned output.

Value

A tibble listing the amino acids substitutions.

Examples

# "sub.txt" is an example file containing missense substitutions formatted
# according to the requirements indicated in http://agvgd.hci.utah.edu/help.php.
my_file <- system.file("extdata", "sub.txt", package = "agvgd")
cat(readLines(my_file), sep = "\n")

read_substitutions(file = my_file)

# lee2010_sub.txt is a file containing the missense variants studied by
# Lee et al. (2010): https://doi.org/10.1158/0008-5472.CAN-09-4563.
read_substitutions(file = system.file("extdata", "lee2010_sub.txt", package = "agvgd"))

# "sub.txt" is an example file containing missense substitutions formatted
# according to the requirements indicated in http://agvgd.hci.utah.edu/help.php.
my_file <- system.file("extdata", "sub.txt", package = "agvgd")
cat(readLines(my_file), sep = "\n")

read_substitutions(file = my_file)

# lee2010_sub.txt is a file containing the missense variants studied by
# Lee et al. (2010): https://doi.org/10.1158/0008-5472.CAN-09-4563.
read_substitutions(file = system.file("extdata", "lee2010_sub.txt", package = "agvgd"))

Convert a residue position to an alignment position

Description

This function converts an residue position to a position in the frame of the alignment.

Usage

res_to_poi(alignment, res)
res_to_poi(alignment, res)

Arguments

`alignment`	An alignment.
`res`	A residue position.

Value

An integer vector of alignment positions corresponding to residue position in the reference sequence.

Examples

align_ATM <- read_alignment('ATM')
align_ATM[, 1:6]

# Convert the positions of the first five residues to alignment positions
res_to_poi(align_ATM, 1:5)

align_ATM <- read_alignment('ATM')
align_ATM[, 1:6]

# Convert the positions of the first five residues to alignment positions
res_to_poi(align_ATM, 1:5)

Export an alignment to FASTA

Description

This function takes an alignment and exports it to a FASTA file.

Usage

write_alignment(alignment, file)
write_alignment(alignment, file)

Arguments

`alignment`	An alignment. It may be a simple matrix or an object obtained with `read_alignment()`.
`file`	A file path.

Value

This function is run for its side effect of writing a file. But it returns the file path passed in file.

Examples


alignment <- matrix(
  c('P', 'M', 'I',
    'P', 'I', 'I',
    'P', 'L', 'I'),
  nrow = 3,
  byrow = TRUE
)

# Export an alignment based on a matrix
write_alignment(alignment, "my_alignment.fasta")
cat(readLines("my_alignment.fasta"), sep = "\n")

# Export one of the bundled alignments
write_alignment(read_alignment(gene = 'BRCA1'), "BRCA1.fasta")
cat(readLines("BRCA1.fasta")[1:10], sep = "\n")


alignment <- matrix(
  c('P', 'M', 'I',
    'P', 'I', 'I',
    'P', 'L', 'I'),
  nrow = 3,
  byrow = TRUE
)

# Export an alignment based on a matrix
write_alignment(alignment, "my_alignment.fasta")
cat(readLines("my_alignment.fasta"), sep = "\n")

# Export one of the bundled alignments
write_alignment(read_alignment(gene = 'BRCA1'), "BRCA1.fasta")
cat(readLines("BRCA1.fasta")[1:10], sep = "\n")

Generate and export a list of substitutions

Description

This function exports to a file a list of residue substitutions. The format used will be the same one as requested by the web version of Align-GVGD.

Usage

write_substitutions(
  file,
  alignment,
  poi,
  sub,
  mode = c("recycle", "expand_grid")
)
write_substitutions(
  file,
  alignment,
  poi,
  sub,
  mode = c("recycle", "expand_grid")
)

Arguments

`file`	A file path.
`alignment`	A character matrix or an alignment object obtained with `read_alignment()`. Rows are expected to be sequences of single characters (protein residues), and columns the alignment positions. The first row must be the reference sequence, i.e. the sequence whose substitutions will be evaluated against.
`poi`	A whole number indicating the position of interest (POI).
`sub`	A character vector of protein residue substitutions to be classified. The amino acids must be provided as one-letter symbols.
`mode`	If both `poi` and `sub` contain more than one element, `mode` specifies how these two inputs are combined. If `mode = 'recycle'` the shortest vector is recycled to match the length of the longest. If `mode = 'expand_grid'`, all combinations between elements of `poi` and `sub` are combined.

Value

This function is run for its side effect of writing a file. But it returns the file path passed in file.

Examples


write_substitutions(file = "ex01.csv",
                    alignment = read_alignment("ATM"),
                    poi = 20:25,
                    sub = amino_acids())
cat(readLines("ex01.csv"), sep = "\n")

write_substitutions(file = "ex02.csv",
                    alignment = read_alignment("ATM"),
                    poi = 20:21,
                    sub = amino_acids(),
                    mode = 'expand_grid')
cat(readLines("ex02.csv"), sep = "\n")

write_substitutions(file = "ex01.csv",
                    alignment = read_alignment("ATM"),
                    poi = 20:25,
                    sub = amino_acids())
cat(readLines("ex01.csv"), sep = "\n")

write_substitutions(file = "ex02.csv",
                    alignment = read_alignment("ATM"),
                    poi = 20:21,
                    sub = amino_acids(),
                    mode = 'expand_grid')
cat(readLines("ex02.csv"), sep = "\n")

Package 'agvgd'

Help Index

Align-GVGD (A-GVGD)

Description

Usage

Arguments

Value

References

Examples

Pre-bundled alignments

Description

Usage

Arguments

Value

Examples

The 20 standard amino acids

Description

Usage

Arguments

Value

Examples

Determine CPV ranges

Description

Usage

Arguments

Value

See Also

Examples

Deviation function

Description

Usage

Arguments

Details

Value

See Also

Examples

Grantham deviation

Description

Usage

Arguments

Value

See Also

Examples

Grantham variation

Description

Usage

Arguments

Value

See Also

Examples

Convert an alignment position to residue position

Description

Usage

Arguments

Value

Examples

Converts a sequence profile to an alignment

Description

Usage

Arguments

Value

Read a protein sequence multiple alignment

Description

Usage

Arguments

Value

Examples

Read a file with amino acid substitutions

Description

Usage

Arguments

Value

Examples

Convert a residue position to an alignment position

Description

Usage

Arguments

Value

Examples

Export an alignment to FASTA