/usr/lib/R/site-library/GenomicRanges/NEWS is in r-bioc-genomicranges 1.14.3-1.
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-------------------------
NEW FEATURES
o Add coercion from GenomicRangesList to RangedDataList.
o Add "c" method for GAlignmentsPairs objects.
o Add coercion from GAlignmentPairs to GAlignmentsList.
o Add 'inter.feature' and 'fragment' arguments to summarizeOverlaps().
o Add seqselect,GAlignments-method.
o Add CIGAR utilities:
explodeCigarOps(), explodeCigarOpLengths()
cigarRangesAlongReferenceSpace(), cigarRangesAlongQuerySpace()
cigarRangesAlongPairwiseSpace(), extractAlignmentRangesOnReference()
cigarWidthAlongReferenceSpace(), cigarWidthAlongQuerySpace()
cigarWidthAlongPairwiseSpace().
o Add seqlevels0() and restoreSeqlevels().
o Add seqlevelsInUse() getter for GRanges, GRangesList, GAlignments
GAlignmentPairs, GAlignmentsList and SummarizedExperiment objects.
o Add update,GAlignments method.
o Add GIntervalTree class.
o Add coercion from GAlignmentPairs to GAlignments.
o Add sortSeqlevels().
o Add tileGenome().
o Add makeGRangesFromDataFrame() and coercion from data.frame or DataFrame
to GRanges.
SIGNIFICANT USER-LEVEL CHANGES
o Renaming (with aliases from old to new names):
- classes
GappedAlignments -> GAlignments
GappedAlignmentPairs -> GAlignmentPairs
- functions
GappedAlignments() -> GAlignments()
GappedAlignmentPairs() -> GAlignmentPairs()
readGappedAlignments() -> readGAlignments()
readGappedAlignmentPairs() -> readGAlignmentPairs()
o Remove 'asProperPairs' argument to readGAlignmentsList().
o Modify "show" method for Seqinfo object to honor showHeadLines
and showTailLines global options.
o 50x speedup or more when merging 2 Seqinfo objects, 1 very small
and 1 very big.
o Add dependency on new XVector package.
o Enhanced examples for renaming seqlevels in seqlevels-utils.Rd.
o More efficient reference class constructor for 'assays'
slot of SummarizedExperiment objects.
o 'colData' slot of SummarizedExperiment produced from call to
summarizedOverlaps() now holds the class type and length of 'reads'.
o 4x speedup to cigarToRleList().
o Relax SummarizedExperiment class validity.
o Renaming (with aliases from old to new names):
cigarToWidth() -> cigarWidthOnReferenceSpace(), and
cigarToQWidth() -> cigarWidthOnQuerySpace().
o Improvements to summarizeOverlaps():
- mode 'Union': 1.5x to 2x speedup
- mode 'IntersectionNotEmpty': 2x to 8x speedup + memory footprint
reduced by ~ half
o Change default 'use.names' to FALSE for readGAlignmentsList().
o Implement 'type="equal"' for findOverlaps,SummarizedExperiment methods.
o Modify summarizeOverlaps() examples to use 'asMates=TRUE' instead
of 'obeyQname=TRUE'.
o Remove unneeded "window" method for GenomicRanges objects.
o Speed up seqinfo() getter and setter on SummarizedExperiment objects
and derivatives (e.g. VCF) by using direct access to 'rowData' slot.
o coverage,GenomicRanges method now uses .Ranges.coverage() when
using the defaults for 'shift' and 'width'.
o Remove restriction that metadata column names must be different on
a GRangesList and the unlisted GRanges.
o GenomicRangesUseCases vignette has been redone and renamed
to GenomicRangesHOWTOs
DEPRECATED AND DEFUNCT
o Defunct all "match" and "%in%" methods in the
package except for those with the GenomicRanges,GenomicRanges signature.
o Deprecate GappedAlignment*:
- GappedAlignments and GappedAlignmentPairs classes
- GappedAlignments() and GappedAlignmentPairs() constructors
- readGappedAlignments() and readGappedAlignmentPairs() functions
o Deprecate cigar util functions:
cigarToWidth(), cigarToQWidth(), cigarToIRanges()
splitCigar(), cigarToIRanges(), cigarToIRangesListByAlignment()
cigarToIRangesListByRName(), cigarToWidth(), cigarToQWidth()
cigarToCigarTable(), summarizeCigarTable()
o Deprecate seqselect().
BUG FIXES
o Fix bug in c,GAlignments for case when objects were unnamed.
o Fix bug in flank,GenomicRanges (when 'ignore.strand=TRUE'
'start' was being set to TRUE).
o Fix bug in behavior of summarizeOverlaps() count mode
'IntersectionNotEmpty' when 'inter.features=FALSE'. Shared
regions are now removed before counting.
o Fix bug in cigarToIRangesListByAlignment() when 'flag' is
supplied and indicates some reads are unmapped.
o Fix bug in summarizeOverlaps(..., mode='IntersectionNotEmpty')
when 'features' has '-' and '+' elements and 'ignore.strand=TRUE'.
o match,GenomicRanges,GenomicRanges method now handles properly objects
with seqlevels not in the same order.
CHANGES IN VERSION 1.12.0
-------------------------
NEW FEATURES
o Implement "seqnameStyle" replacement method for Seqinfo object.
'seqnameStyle(x) <- style' works on any object with a "seqinfo"
replacement method.
o Add trim,GenomicRanges-method to trim out of bound ranges.
o Add promoters,GenomicRanges and promoters,GRangesList methods.
o Add "overlapsAny" methods as a replacement for the deprecated
"%in%" methods.
o Add 'ignore.strand' argument to match,GenomicRanges-method.
o Add 'with.mapping' argument to "reduce" method for GenomicRanges
objects.
o Add "unname" method to remove dimnames from SummarizedExperiment.
o Add "cbind" and "rbind" methods for SummarizedExperiment.
o Add "seqselect", "seqselect<-" and "split" methods for
SummarizedExperiment.
o Add GAlignmentsList class.
o Add readGAlignmentsList generic and methods.
SIGNIFICANT USER-LEVEL CHANGES
o resize,GenomicRanges method no longer checks that 'fix' is
length-compatible with 'x' when 'x' is length zero. This
allows for resize(x, w, fix = "end") without worrying about
'x' being zero-length.
o Change the behavior of "distance". Previously adjacent ranges
had a distance of 1 and overlapping had a distance of 0. Now
both adjacent AND overlapping have a distance of 0.
o shift,GenomicRanges-method no longer trims out of bound ranges.
o "distanceToNearest" no longer drops ranges that have no hit
but returns 'NA' for 'subjectHits' and 'distance'.
o "genome" is no longer an invalid metadata colname for GenomicRanges
objects.
o 4x-8x speedup for doing coverage() on a GRanges or GRangesList with
many seqlevels.
o Remove ">=", "<", and ">" methods for GenomicRanges objects.
o Speedup "seqinfo" setters for GenomicRanges and GappedAlignments
by avoiding validation when not necessary.
o readGappedAlignments can now pass a BamFile to readBamGappedAlignments.
o Remove unneeded "unique" and "sort" methods for GenomicRanges objects.
o Change behavior of "match" and "%in%" on GenomicRanges objects to use
equality instead of overlap for comparing elements between GenomicRanges
objects 'x' and 'table'.
o match,GenomicRanges-method gets the same 'method' argumnet as the
"duplicated" method for these objects.
o Remove unneeded "countOverlaps" methods.
o "classNameForDisplay" shortens the name of data type when displayed.
o Add global options 'showHeadLines' and 'showTailLines' to
control the number of head/tails lines displayed in
show,GRanges and show,GappedAlignments methods.
o "distanceToNearest" now returns a Hits object instead of DataFrame.
DEPRECATED AND DEFUNCT
o Remove defunct countGenomicOverlaps(), grg(), and globalToQuery()
o Defunct previously deprecated '.ignoreElementMetadata' argmuent
of c,GenomicRanges-method.
o Deprecate all "match" and "%in%" methods in the package except for
those with the GenomicRanges,GenomicRanges signature.
o Deprecate "resolveHits" methods.
BUG FIXES
o Several bug fixes to "nearest".
o Output of "findSpliceOverlaps" now displays 'NA' for ranges with
no hits.
CHANGES IN VERSION 1.10.0
-------------------------
NEW FEATURES
o SummarizedExperiment gains direct GRanges / GRangesList
interface to rowData.
o Add "distanceToNearest" method for GenomicRanges objects.
o SummarizedExperiment class can now be subset by row when there are no
'columns', and by column when there are no 'rows'.
o Add 'drop.D.ranges' argument to coverage,GappedAlignments and
coverage,GappedAlignmentPairs methods.
o findOverlaps() now supports 'select="last"' and 'select="arbitrary"' (in
addition to 'select="all"' and 'select="first"') on GenomicRanges
objects.
o summarizeOverlaps(..., mode="IntersectionStrict") now handles circular
chromosomes. A warning is issued and circular chromosomes in 'reads' are
omitted from counting.
o Add disjoin,GRangesList method.
o Add findSpliceOverlaps() for identifyng ranges (reads) that are
compatible with a specific transcript isoform (the non-compatible
ranges are analyzed for the presence of novel splice events).
o Add ngap,GappedAlignmentPairs method.
o Add introns() generic with methods for GappedAlignments and
GappedAlignmentPairs objects.
o No more arbitrary max of 3 gaps per read in isCompatibleWithSplicing()
and isCompatibleWithSkippedExons().
o Add findCompatibleOverlaps() and countCompatibleOverlaps().
o Passing '...' down through as.data.frame(GRanges, ...) so user can tweak
stringsAsFactors default for metadata columns.
o Add extractSteppedExonRanks(), extractSpannedExonRanks() and
extractQueryStartInTranscript() utilities (work with single- and
paired-end reads).
o Add 'flip.query.if.wrong.strand' arg (FALSE by default) to
"encodeOverlaps" method for GRangesList objects.
o Add makeSeqnameIds() low-level utility.
SIGNIFICANT USER-LEVEL CHANGES
o SummarizedExperiment rowData and assays operations have
significant performance improvements.
o mcols() is now the preferred way (over elementMetadata() or values()) to
access the metadata columns of a GenomicRanges, GRangesList,
GappedAlignments, GappedAlignmentPairs, SummarizedExperiment object,
or any Vector object. elementMetadata() and values() might go away at
some point in the (not so close) future.
o Add "$" and "$<-" methods for GenomicRanges *only*. Provided as a
convenience and as the result of strong popular demand. Note that those
methods are not consistent with the other "$" and "$<-" methods in the
IRanges/GenomicRanges infrastructure, and might confuse some users by
making them believe that a GenomicRanges object can be manipulated as a
data.frame-like object. It is therefore recommended to use them only
interactively, and their use in scripts or packages is discouraged.
For the latter, use 'mcols(x)$name' instead of 'x$name'.
o No more warning when doing as(x, "GRanges") on a RangedData object with
no "strand" column.
o Refactor "[" method for GenomicRanges objects. The new implementation
always preserves the names of the selected elements instead of trying
to return a GenomicRanges object with unique names. This new behavior
is consistent with subsetting of ordinary vectors and other Vector
objects defined in IRanges/GenomicRanges. Also modify "seqselect" method
for GenomicRanges objects so it also preserves the names of the selected
elements (and thus remains consistent with new behavior of "[" method for
GenomicRanges objects).
o No more names on the integer vector returned by "ngap" method for
GappedAlignments objects.
o Many improvements to the "Overlap encodings" vignette.
o Remove 'param' argument from summarizeOverlaps() generic.
DEPRECATED AND DEFUNCT
o Defunct previously deprecated grg() function.
o Defunct previously deprecated countGenomicOverlaps() generic and methods.
BUG FIXES
o Fix several issues with "precede", "follow", "nearest", and "distance"
methods for GenomicRanges objects.
o Fix bug in summarizeOverlaps(..., ignore.strand=TRUE).
o 6x speedup (and a 6x memory footprint reduction) or more when using
encodeOverlaps() on big GRangesList objects.
o Fix bug in renameSeqlevels() wrt order of rename vector.
o Fix bug in selectEncodingWithCompatibleStrand().
CHANGES IN VERSION 1.8.0
------------------------
NEW FEATURES
o Add GappedAlignmentPairs class (with accessors first(), last(), left(),
right(), seqnames(), strand(), isProperPair()), and
readGappedAlignmentPairs() for dealing with paired-end reads.
Most of the GappedAlignments functionalities (e.g. coercion to
GRangesList, "findOverlaps" and related methods, "coverage", etc...)
work on a GappedAlignmentPairs object.
o Add encodeOverlaps,GRangesList,GRangesList,missing and related utilities
flipQuery(), selectEncodingWithCompatibleStrand(),
isCompatibleWithSplicing(), isCompatibleWithSkippedExons() and
extractSkippedExonRanks().
o Add 'order.as.in.query' arg to grglist() and rglist().
o SummarizedExperiment gains direct access to colData columns with
$, $<-, [[, and [[<- methods
o Add map,GenomicRanges,GRangesList and
map,GenomicRanges,GappedAlignments methods. These allow mapping
from genome space to transcript space, and genome space to read
space, respectively.
o Add seqinfo methods (and friends) for RangedData, RangesList,
and other IRanges data structures. These use metadata(x)$seqinfo.
o Add disjointBins,GenomicRanges.
o Add score,GRangesList and score,GenomicRanges (gets the score column
like for RangedData).
o Add RangedDataList -> GenomicRangesList coercion.
o Add RleViewsList -> GRanges coercion.
o Add pintersect,GRangesList,GRangesList
o Add stack,GenomicRangesList
o ignore.strand argument now more uniformly supported on set operations.
o Add Ops,GenomicRanges (from rtracklayer).
o Add strand,Rle (only logical-Rle is supported).
o Add compare,GenomicRanges
o Add 'drop.empty.ranges' arg (FALSE by default) to low-level cigar
utilities cigarToIRanges(), cigarToIRangesListByAlignment(), and
cigarToIRangesListByRName().
o Add 'reduce.ranges' arg to cigarToIRangesListByAlignment().
SIGNIFICANT USER-LEVEL CHANGES
o grglist,GappedAlignments now carries over metadata columns.
o Names are no longer forced to be unique when unlisting a
GRangesList with use.names=TRUE.
o seqnames() is now preferred over rname() on a GappedAlignments object.
o cigarToIRangesListByAlignment() now returns a CompressedIRangesList
instead of CompressedNormalIRangesList.
o Low-level CIGAR utilities now ignore CIGAR operation P (instead of
trowing an error).
o The 'weight' arg in "coverage" method for GenomicRanges objects now
can also be a single string naming a column in elementMetadata(x).
o Ranges outside the sequences bounds of the underlying sequences are now
accepted (with a warning) in GenomicRanges/GRangesList/GappedAlignments
objects.
o When called with 'ignore.strand=TRUE', the "range" and "disjoin" methods
for GenomicRanges objects now behave like if they set the strand of the
input to "*" before they do any computation.
o When called with 'ignore.strand=TRUE', "reduce" method for GenomicRanges
objects, and "union", "intersect" and "setdiff" methods for GRanges
objects now set the strand of their arguments to "*" prior to any
computation.
o No more mangling of the names when combining GRanges objects ("c" method
for GRanges objects was trying to return unique names).
o Remove isCircularWithKnownLength() generic and methods (nobody knows,
uses, or needs this).
BUG FIXES
o flank,GRangesList no longer forces 'use.names' to TRUE and 'both' to
FALSE.
o range,GenomicRanges was broken when object had no ranges
o Fix integer overflow issue that can occur in cigarQNarrow() or
cigarQNarrow() when the cigar vector is very long.
CHANGES IN VERSION 1.6.0
------------------------
NEW FEATURES
o seqlevels() and seqinfo() setters have a new arg ('force', default is
FALSE) to force dropping sequence levels currently in use.
o Seqinfo objects now have a genome column that can be accessed with
genome() getter/setter.
o "pgap" method for c(x="GRanges", y="GRanges").
o Add comparison (==, <=, duplicated, unique, etc...) and ordering
(order, sort, rank) methods for GenomicRanges objects.
o Add "flank" method for GRangesList objects.
o Add "isDisjoint" and "restrict" methods for GRanges and GRangesList
objects.
o Add GRangesList constructor makeGRangesListFromFeatureFragments().
o Add "names" and "names<-" methods for GappedAlignments objects.
o Add 'ignore.strand' arg to a number of methods:
- findOverlaps,GRangesList,RangesList
- findOverlaps,GappedAlignments,ANY
- findOverlaps,ANY,GappedAlignments
o 'shift' and 'weight' arguments of "coverage" method for GenomicRanges
objects now can be numeric vectors in addition to lists.
o Add "c" method for GappedAlignments objects.
SIGNIFICANT USER-VISIBLE CHANGES
o readGappedAlignments() supports 2 new arguments: (1) 'use.names' (default
is FALSE) for using the query template names (QNAME field in a SAM/BAM
file) to set the names of the returned object, and (2) 'param' (default
is NULL, otherwise a ScanBamParam object) for controlling what fields and
which records are imported. readGappedAlignments() doesn't support
the 'which' arg anymore.
o The names of a GRanges/GRangesList/GappedAlignments object are not
required to be unique anymore.
o By default, the rownames are not set anymore on the DataFrame returned
by elementMetadata() on a GRanges/GRangesList/GappedAlignments object.
o 'width' arg of "coverage" method for GenomicRanges objects now must be
NULL or numeric vector (instead of NULL or list).
DEPRECATED AND DEFUNCT
o Deprecate countGenomicOverlaps() in favor of summarizeOverlaps().
o Deprecate grg() in favor of granges().
BUG FIXES
o Fix bug in "pintersect" methods operating on GappedAlignments objects.
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