Changes in version 2.1.6 (2025-09-18)                  

  - Remove dependency on C++11.

                 Changes in version 2.1.5 (2022-10-18)                  

  - Bug fix: Use && instead of & in C++ source.

                 Changes in version 2.1.4 (2022-02-11)                  

  - Use unnamed formula argument in aggregate() to account for change in
    R.

                 Changes in version 2.1.2 (2021-08-10)                  

  - DOUBLE_EPS -> DOUBLE_EPSILON.
  - Modified citation to point to Heredity.
  - Adds notes about the necessity of using adaptive priors in ldfast().

                 Changes in version 2.1.0 (2021-06-11)                  

  - Includes a win argument in ldfast(), which implements the
    moment-based LD correction along a sliding window.
  - Fixes a bug where monomorphic SNPs were causing errors when type =
    "Dprime" was selected in ldfast(). Now we just return NA's for LD
    with monomorphic SNPs.
  - Uses the complete reference of Gerard (2021)
    (doi:10.1111/1755-0998.13349)

                 Changes in version 2.0.2 (2021-02-17)                  

  - Removes ldfast_old() and ldfast_calc(), which were not used in any
    exported functions, because these functions had memory issues,
    detected by valgrind.

                 Changes in version 2.0.1 (2021-02-12)                  

  - Added ldfast(), a new LD estimation approach based on sample moments
    of marginal posterior genotype moments.
  - Unlike ldest(), mldest(), and sldest(), the new approach implemented
    in ldfast() is scalable to genome-wide applications, as these new
    estimators can be calculated in linear time in the sample size.
  - Citation of MLE approach points to MER article.

                 Changes in version 1.1.0 (2020-11-14)                  

  - I have changed the terminology from "gametic LD" to "haplotypic" LD,
    and so all instances of "gametic" have changed to "haplotypic". A
    breaking change is that all options that were "gam" are now "hap".
  - Fixed an issue where the title in plot.lddf() was being cut off.
  - Added a reference to the preprint where the methodology is
    developed.
  - Updated the vignette to also take a user through uploading a VCF
    file into R using the VariantAnnotation package. We also provided
    examples on formatting genotype likelihoods from updog and fitpoly.

                 Changes in version 1.0.0 (2020-08-02)                  

  - Initial release of package.