createSubstitutionMatrix {shazam}R Documentation

Builds a substitution model

Description

createSubstitutionMatrix builds a 5-mer nucleotide substitution model by counting the number of substitution mutations occuring in the center position for all 5-mer motifs.

Usage

createSubstitutionMatrix(
  db,
  model = c("s", "rs"),
  sequenceColumn = "sequence_alignment",
  germlineColumn = "germline_alignment_d_mask",
  vCallColumn = "v_call",
  multipleMutation = c("independent", "ignore"),
  returnModel = c("5mer", "1mer", "1mer_raw"),
  minNumMutations = 50,
  numMutationsOnly = FALSE
)

Arguments

db

data.frame containing sequence data.

model

type of model to create. The default model, "s", builds a model by counting only silent mutations. model="s" should be used for data that includes functional sequences. Setting model="rs" creates a model by counting both replacement and silent mutations and may be used on fully non-functional sequence data sets.

sequenceColumn

name of the column containing IMGT-gapped sample sequences.

germlineColumn

name of the column containing IMGT-gapped germline sequences.

vCallColumn

name of the column containing the V-segment allele call.

multipleMutation

string specifying how to handle multiple mutations occuring within the same 5-mer. If "independent" then multiple mutations within the same 5-mer are counted indepedently. If "ignore" then 5-mers with multiple mutations are excluded from the total mutation tally.

returnModel

string specifying what type of model to return; one of c("5mer", "1mer", "1mer_raw"). If "5mer" (the default) then a 5-mer nucleotide context model is returned. If "1mer" or "1mer_raw" then a single nucleotide substitution matrix (no context) is returned; where "1mer_raw" is the unnormalized version of the "1mer" model. Note, neither 1-mer model may be used as input to createMutabilityMatrix.

minNumMutations

minimum number of mutations required to compute the 5-mer substitution rates. If the number of mutations for a 5-mer is below this threshold, its substitution rates will be estimated from neighboring 5-mers. Default is 50. Not required if numMutationsOnly=TRUE.

numMutationsOnly

when TRUE, return counting information on the number of mutations for each 5-mer, instead of building a substitution matrix. This option can be used for parameter tuning for minNumMutations during preliminary analysis. Default is FALSE. Only applies when returnModel is set to "5mer". The data.frame returned when this argument is TRUE can serve as the input for minNumMutationsTune.

Details

Caution: The targeting model functions do NOT support ambiguous characters in their inputs. You MUST make sure that your input and germline sequences do NOT contain ambiguous characters (especially if they are clonal consensuses returned from collapseClones).

Value

For returnModel = "5mer":

When numMutationsOnly is FALSE, a 4x1024 matrix of column normalized substitution rates for each 5-mer motif with row names defining the center nucleotide, one of c("A", "C", "G", "T"), and column names defining the 5-mer nucleotide sequence.

When numMutationsOnly is TRUE, a 1024x4 data frame with each row providing information on counting the number of mutations for a 5-mer. Columns are named fivemer.total, fivemer.every, inner3.total, and inner3.every, corresponding to, respectively, the total number of mutations when counted as a 5-mer, whether there is mutation to every other base when counted as a 5-mer, the total number of mutations when counted as an inner 3-mer, and whether there is mutation to every other base when counted as an inner 3-mer.

For returnModel = "1mer" or "1mer_raw": a 4x4 normalized or un-normalized 1-mer substitution matrix respectively.

References

  1. Yaari G, et al. Models of somatic hypermutation targeting and substitution based on synonymous mutations from high-throughput immunoglobulin sequencing data. Front Immunol. 2013 4(November):358.

See Also

extendSubstitutionMatrix, createMutabilityMatrix, createTargetingMatrix, createTargetingModel, minNumMutationsTune.

Examples


# Subset example data to one isotype and sample as a demo
data(ExampleDb, package="alakazam")
db <- subset(ExampleDb, c_call == "IGHA" & sample_id == "-1h")[1:25,]

# Count the number of mutations per 5-mer
subCount <- createSubstitutionMatrix(db, sequenceColumn="sequence_alignment",
                                     germlineColumn="germline_alignment_d_mask",
                                     vCallColumn="v_call",
                                     model="s", multipleMutation="independent",
                                     returnModel="5mer", numMutationsOnly=TRUE)

# Create model using only silent mutations
sub <- createSubstitutionMatrix(db, sequenceColumn="sequence_alignment",
                                germlineColumn="germline_alignment_d_mask",
                                vCallColumn="v_call",
                                model="s", multipleMutation="independent",
                                returnModel="5mer", numMutationsOnly=FALSE,
                                minNumMutations=20)



[Package shazam version 1.2.0 Index]