CHANGES IN VERSION 1.6.0
-------------------------

    o `seqFitNullGLMM_SPA()` can use imputed dosages directly without
      converting the dosages to the best-guess genotypes

    o new function `glmmHeritability()` for approximate heritability estimates


CHANGES IN VERSION 1.4.0
-------------------------

    o set-based tests: burden, ACAT-V


CHANGES IN VERSION 1.2.2
-------------------------

    o update the citation

    o work around gcc-10


CHANGES IN VERSION 1.2.0
-------------------------

    o `seqAssocGLMM_SPA()` can save to a RDS file


CHANGES IN VERSION 1.0.2
-------------------------

    o fix an issue when there is no covariate in the formula (e.g., y ~ 1)


CHANGES IN VERSION 1.0.1
-------------------------

    o add a new option for the threshold of missing variant to
      `seqAssocGLMM_SPA()`

    o change the output column 'AC.alt' to 'mac' in `seqAssocGLMM_SPA()`

    o retry model fitting at least 10 times if matrix is singular or not
      positive definite, or large variance is observed


CHANGES IN VERSION 1.0.0
-------------------------

    o first Bioconductor release


CHANGES IN VERSION 0.99.0 (10-02-2019)
-------------------------

    o package submitted to Bioconductor


CHANGES IN VERSION 0.9.10 (08-12-2019)
-------------------------

    o SAIGE algorithm implementation for quantitative outcomes


CHANGES IN VERSION 0.9.9 (07-24-2019)
-------------------------

    o add a vignette to the package

    o the default of random number generator changes in R: "Rounding" was the
      default in `RNGkind()` prior to R_3.6.0, but "Rejection" is used in
      R (>= v3.6.0). For reproduction of the results created by R (< v3.6.0),
      please use `RNGkind("Mersenne-Twister", "Inversion", "Rounding")` in
      R (>= v3.6.0)


CHANGES IN VERSION 0.9.7 (06-08-2019)
-------------------------

    o seqAssocGLMM_SPA(): load balancing in parallel


CHANGES IN VERSION 0.9.0 (01-07-2019)
-------------------------

    o first version of SAIGEgds
