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 element metadata.

    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.