Changes in version 1.5.19                        

  - Remove speedglm dependency as it was removed from CRAN (April 2023).

                       Changes in version 1.1.13                        

  - Bug fix that allows nearest matching method to handle categorical
    (or categorical-like) covariates.

                        Changes in version 1.1.4                        

  - Needed to drop features that have 0 width after trimming in
    bootRanges.
  - Made the validity test for bootRanges only look for iter.

                        Changes in version 1.1.1                        

  - Change to factor-Rle output for bootRanges to simplify the
    downstream plyranges.

                        Changes in version 1.0.0                        

  - nullranges is released on Bioconductor! the package offers the
    creation of null genomic feature sets, either through sampling from
    a pool in order to match covariates with a particular focal set, or
    via block bootstrapping of features optionally with respect to a
    genome segmentation. Critically, nullranges is designed as a modular
    package, solely for the purpose of generating null feature sets, and
    to be used in conjunction with another package for calculating
    overlaps, such as GenomicRanges or plyranges. Let us know your
    comments, suggestions or feedback on Bioconductor support site or
    through GitHub Issues.