General:
New feature:
convertNumbering to convert between
numbering systems (IMGT, Kabat).Mutation Profiling:
shmulateTree has new argument nproc to
specify the number of cores. Default values mutThresh and
windowSize have been set to mutThresh=6 and
windowSize=10.
Added the option plotFiltered=NULL to
slideWindowTunePlot.
Fixed a bug in listObservedMutations not returning a
list when db had one sequence with one mutation.
Fixed bars shifted in plotMutability.
General:
Selection Analysis:
observedMutations, expectedMutations, and
calcBaseline can analyze mutations in all regions (CDR1,
CDR2, CDR3, FWR1, FWR2, FWR3 and FWR4) by specifying
regionDefinition=IMGT_VDJ or
regionDefinition=IMGT_VDJ_BY_REGIONS.setRegionBoundaries to build
sequence-specific RegionDefinition objects extending to
CDR3 and FWR4.makeGraphDf to facilitate mutational
analysis on lineage trees.Distance Profiling:
distToNearest where TRB and TRD
sequences where ignored in distance calculation.distToNearest causing a fatal error when
cross was set.nearestDist causing a fatal error when
using model="aa" and crossGroups.Targeting Models:
plotMutability.Mutation Profiling:
observedMutations and
calcObservedMutations causing mutation counting to fail
when there are gap (-) characters in the germline
sequence.Targeting Models:
createTargetingModel causing empty
counts in the numMutS and numMutR slots.Distance Profiling:
distToNearest.groupUsingOnlyIGH argument of
distToNearest to onlyHeavy.Backwards Incompatible Changes:
V_CALL (Change-O) as the default to
identify the field that stored the V gene calls, they now use
v_call (AIRR). That means, scripts that relied on default
values (previously, v_call="V_CALL"), will now fail if
calls to the functions are not updated to reflect the correct value for
the data. If data are in the Change-O format, the current default value
v_call="v_call" will fail to identify the column with the V
gene calls as the column v_call doesn’t exist. In this
case, v_call="V_CALL" needs to be specified in the function
call.ExampleDb converted to the AIRR Rearrangement standard
and examples updated accordingly.labels slot of
IMGT_V has changed from CDR_R,
CDR_S, FWR_R and FWR_S to
cdr_r, cdr_s, fwr_r and
fwr_s, respectively.CODON_TABLE and the different
MUTATION_SCHEMES change from R, S
and Stop to r, s and
stop, respectively.MU_COUNT_SEQ to mu_count_seq.calcBaseline and related function output columns and S4
object slots. For example, from PVALUE, REGION
and BASELINE_CI_PVALUE to pvalue,
region and baseline_ci_pvalue,
respectively.createSubstitutionMatrix,
createMutabilityMatrix and
createTargetingModel, changed from
model=c("S","RS") to model=c("s","rs").General:
Targeting Models:
createMutabilityMatrix,
extendMutabilityMatrix, createTargetingMatrix,
and createTargetingModel now also returns the numbers of
silent and replacement mutations used for estimating the 5-mer
mutabilities. These numbers are recorded in the numMutS and
numMutR slots in the newly defined
MutabilityModel, MutabilityModelWithSource,
and TargetingMatrix classes.Mutation Profiling:
shmulateSeq now also supports specifying the frequency
of mutations to be introduced. (Previously, only the number of mutations
was supported.)General:
General:
Distance Calculation:
distToNearest that could potentially
cause sequences from different partitions to be used for distance
calculation.General:
Distance Calculation:
plotDensityThreshold for negative
densities.distToNearest for performing subsampling
while calculating cross-group nearest neighbor distances.distToNearest now supports,
via a new argument VJthenLen, either a 2-stage partitioning
(first by V gene and J gene, then by junction length), or a 1-stage
partitioning (simultaneously by V gene, J gene, and junction length).
For 1-stage partitioning, distToNearest supports export of
the partitioning information as a new column via
keepVJLgroup.distToNearest now supports single-cell input data with
the addition of new arguments cellIdColumn,
locusColumn, and groupUsingOnlyIGH.Mutation Profiling:
shmulateTree has new arguments, start and
end, to specify the region in the sequence where mutations
can be introduced.Selection Analysis:
consensusSequence which can be used
to build a consensus sequence using a variety of methods.General:
TargetingModel and RegionDefinition S4
classes.General:
subsample argument to distToNearest
function.alakazam. Specifically, progressBar,
getBaseTheme and checkColumns.clearConsole, getnproc, and
getPlatform functions.Distance Calculation:
findThreshold method to
density.density method by
retuning the bandwidth detection process. The density
method should now also yield more consistent thresholds, on
average.subsample argument to findThreshold
now applies to both the density and gmm
methods. Subsampling of distance is not performed by default.plotDensityThreshold and
plotGmmThreshold wherein the breaks argument
was ignored when specifying xmax and/or
xmin.Selection Analysis:
plotBaselineDensity arising
when the groupColumn and idColumn arguments
were set to the same column.sizeElement argument to
plotBaselineDensity to control line sizefield_name argument to field
in editBaseline.Selection Analysis:
plotBaselineDensity which caused an
empty plot to be generated if there was only a single value in the
idColumn.calcBaseline which caused a crash in
summarizeBaseline and groupBaseline when input
baseline is based on only 1 sequence (i.e. when
nrow(baseline@db) is 1).plot call on a Baseline object
to plotBaselineDensity.getBaselineStats function.summary method for Baseline
objects that calls summarizeBaseline and returns a
data.frame.Mutation Profiling:
shmulateSeq which caused a crash when
the input sequence contains gaps (.).mutations in
shmulateSeq to numMutations.shmulateSeq and
shmulateTree.calcExpectedMutations will now treat non-ACTG
characters as Ns rather than produce an error.RegionDefinition objects for the full V
segment as single region (IMGT_V_BY_SEGMENTS) and the V
segment with each codon as a separate region
(IMGT_V_BY_CODONS).Targeting Models:
calculateMutability function which computes
the aggregate mutability for sequences.createSubstitutionMatrix to
fail for data containing only a single V family.model="S") in createSubstitutionMatrix,
createSubstitutionMatrix and
createTargetingModelplot call on a TargetingModel
object to plotMutability.General:
Distance Calculation:
"gmm" method of
findThreshold() that allows users to choose a mixture of
two univariate density distribution functions among four available
combinations: "norm-norm", "norm-gamma","gamma-norm", or "gamma-gamma"."gmm" method of findThreshold() from the best
average sensitivity and specificity, the curve intersection or user
defined sensitivity or specificity.cutEdge argument of
findThreshold() to edge.Mutation Profiling:
collapseClones(), adding various
deterministic and stochastic methods to obtain effective clonal
sequences, support for including ambiguous IUPAC characters in output,
as well as extensive documentation. Removed
calcClonalConsensus() from exported functions.observedMutations() and
calcObservedMutations().calcObservedMutations() for sequences with
non-triplet overhang at the tail.OBSERVED) and expected mutations (previously
EXPECTED) returned by observedMutations() and
expectedMutations() to MU_COUNT and
MU_EXPECTED respectively.Selection Analysis:
calcBaseline() no longer calls
collapseClones() automatically if a CLONE
column is present. As indicated by the documentation for
calcBaseline() users are advised to obtain effective clonal
sequences (for example, calling collapseClones()) before
running calcBaseline().calcBaseline().Mutation Profiling:
collapseClones() that prevented it from
running when nproc is greater than 1.General:
Mutation Profiling:
collapseClones() that resulted in
erroneous CLONAL_SEQUENCE and CLONAL_GERMLINE
being returned.observedMutations was
running.General:
Selection Analysis:
summarizeBaseline(). The returned p-value can now be either
positive or negative. Its magnitude (without the sign) should be
interpreted as per normal. Its sign indicates the direction of the
seLicense chalection detected. A positive p-value indicates positive
selection, whereas a negative p-value indicates negative selection.editBaseline() to exported functions, and a
corresponding section in the vignette.calcBaseline().Targeting Models:
numMutationsOnly argument to
createSubstitutionMatrix(), enabling parameter tuning for
minNumMutations.minNumMutationsTune() and
minNumSeqMutationsTune() to tune for parameters
minNumMutations and minNumSeqMutations in
functions createSubstitutionMatrix() and
createMutabilityMatrix() respectively. Also added function
plotTune() which helps visualize parameter tuning using the
abovementioned two new functions.HKL_S5F).HS5FModel as HH_S5F,
MRS5NFModel as MK_RS5NF, and
U5NModel as U5N.HH_S1F), human kappa and lambda light chain, silent,
1-mer, functional substitution model (HKL_S1F), and mouse
kappa light chain, replacement and silent, 1-mer, non-functional
substitution model (MK_RS1NF).makeDegenerate5merSub and
makeDegenerate5merMut which make degenerate 5-mer
substitution and mutability models respectively based on the 1-mer
models. Also added makeAverage1merSub and
makeAverage1merMut which make 1-mer substitution and
mutability models respectively by averaging over the 5-mer models.Mutation Profiling:
returnRaw argument to
calcObservedMutations(), which if true returns the
positions of point mutations and their corresponding mutation types, as
opposed to counts of mutations (hence “raw”).slideWindowSeq() and
slideWindowDb() which implement a sliding window approach
towards filtering a single sequence or sequences in a data.frame which
contain(s) equal to or more than a given number of mutations in a given
number of consecutive nucleotides.slideWindowTune() which allows for
parameter tuning for using slideWindowSeq() and
slideWindowDb().slideWindowTunePlot() which
visualizes parameter tuning by slideWindowTune().Distance Calculation:
distToNearest wherein
normalize="length" for 5-mer models was resulting in
distances normalized by junction length squared instead of raw junction
length.distToNearest wherein
symmetry="min" was calculating the minimum of the total
distance between two sequences instead of the minimum distance at each
mutated position.findThreshold function to infer clonal distance
threshold from nearest neighbor distances returned by
distToNearest.length option for the
normalize argument of distToNearest to
len so it matches Change-O.HS1FDistance and
M1NDistance distance models, which have been renamed to
hs1f_compat and m1n_compat in the
model argument of distToNearest. These
deprecated models should be used for compatibility with DefineClones in
Change-O v0.3.3. These models have been replaced by replaced by
hh_s1f and mk_rs1nf, which are supported by
Change-O v0.3.4.hs5f model in distToNearest to
hh_s5f.MK_RS5NF models to
distToNearest.calcTargetingDistance() to enable calculation
of a symmetric distance matrix given a 1-mer substitution matrix
normalized by row, such as HH_S1F.findThreshold. The previous smoothed
density method is available via the method="density"
argument and the new GMM method is available via
method="gmm".plotGmmThreshold and
plotDensityThreshold to plot the threshold detection
results from findThreshold for the "gmm" and
"density" methods, respectively.Region Definition:
IMGT_V_NO_CDR3 and
IMGT_V_BY_REGIONS_NO_CDR3. Updated IMGT_V and
IMGT_V_BY_REGIONS so that neither includes CDR3 now.Selection Analysis:
Targeting Models:
numSeqMutationsOnly argument to
createMutabilityMatrix(), enabling parameter tuning for
minNumSeqMutations.General:
InfluenzaDb data object, in favor of the
updated ExampleDb provided in alakazam 0.2.4.Distance Calculation:
cross argument to
distToNearest() which allows restriction of distances to
only distances across samples (ie, excludes within-sample
distances).mst flag to distToNearest(), which
will return all distances to neighboring nodes in a minimum spanning
tree.aa model of distToNearest().aa model of
distToNearest().Mutation Profiling:
MutationDefinition
VOLUME_MUTATIONS.shmulateSeq() and
shmulateTree() to simulate mutations on sequences and
lineage trees, respectively, using a 5-mer targeting model.collapseByClone,
calcDbExpectedMutations and
calcDbObservedMutations to collapseClones,
expectedMutations, and observedMutations,
respectively.Selection Analysis:
Baseline object through
groupBaseline() multiple times resulted in incorrect
normalization.title options to
plotBaselineSummary() and
plotBaselineDensity().plotBaselineSummary() and
plotBaselineDensity().testBaseline() function to test the
significance of differences between two selection distributions.General:
InfluenzaDb.dplyr::tbl_df object instead of a
data.frame.Distance Calculation:
distToNearest() did not return the
nearest neighbor with a non-zero distance.Targeting Models:
createSubstitutionMatrix(),createMutabilityMatrix(), and
plotMutability().plotMutability().Mutation Profiling:
MutationDefinition objects
MUTATIONS_CHARGE, MUTATIONS_HYDROPATHY,
MUTATIONS_POLARITY providing alternate approaches to
defining replacement and silent annotations to mutations when calling
calcDBObservedMutations() and
calcDBExpectedMutations().regionDefinition=NULL consistent
for all mutation profiling functions. Now the entire sequence is used as
the region and calculations are made accordingly.calcDBObservedMutations() returns R and S mutations
also when regionDefinition=NULL. Older versions reported
the sum of R and S mutations. The function will add the columns
OBSERVED_SEQ_R and OBSERVED_SEQ_S when
frequency=FALSE, and MU_FREQ_SEQ_R and
MU_FREQ_SEQ_R when frequency=TRUE.General:
Distance Calculation:
symmetry parameter to distToNearest to change
behavior of how asymmetric distances (A->B != B->A) are combined
to get distance between A and B.Mutation Profiling:
Selection Analysis:
Targeting Models:
minNumMutations parameter to
createSubstitutionMatrix. This is the minimum number of observed 5-mers
required for the substituion model. The substitution rate of 5-mers with
fewer number of observed mutations will be inferred from other
5-mers.minNumSeqMutations parameter to
createMutabilityMatrix. This is the minimum number of mutations required
in sequences containing the 5-mers of interest. The mutability of 5-mers
with fewer number of observed mutations in the sequences will be
inferred.returnModel parameter to
createSubstitutionMatrix. This gives user the option to return 1-mer or
5-mer model.returnSource parameter to createMutabilityMatrix.
If TRUE, the code will return a data frame indicating whether each 5-mer
mutability is observed or inferred.Initial public release.
General:
Influenza.tab file did not
load on Mac OS X.citation("shazam") command.Distance Calculation:
HS1FDistance,
based on the Yaari et al, 2013 data.hs1f as the default distance model for
distToNearest().distToNearest().Mutation Profiling:
calcDBClonalConsensus() so that the
function now works correctly when called with the argument
collapseByClone=FALSE.frequency argument to
calcObservedMutations() and
calcDBObservedMutations(), which enables return of mutation
frequencies rather the default of mutation counts.Targeting Models:
M3NModel and all options for using said
model.createSubstitutionMatrix() and
createMutabilityMatrix() where IMGT gaps were not being
handled.General:
Targeting Models:
Targeting Models:
U5NModel, which is a uniform 5-mer
model.plotMutability() output.Prerelease for review.