%global __brp_check_rpaths %{nil}
%global packname  pureseqtmr
%global packver   1.2
%global rlibdir   /usr/local/lib/R/library

Name:             R-CRAN-%{packname}
Version:          1.2
Release:          1%{?dist}%{?buildtag}
Summary:          Predict Transmembrane Protein Topology

License:          GPL-3
URL:              https://cran.r-project.org/package=%{packname}
Source0:          %{url}&version=%{packver}#/%{packname}_%{packver}.tar.gz


BuildRequires:    R-devel >= 3.5.0
Requires:         R-core >= 3.5.0
BuildArch:        noarch
BuildRequires:    R-CRAN-ggplot2 
BuildRequires:    R-CRAN-plyr 
BuildRequires:    R-CRAN-rappdirs 
BuildRequires:    R-CRAN-stringr 
BuildRequires:    R-CRAN-tibble 
Requires:         R-CRAN-ggplot2 
Requires:         R-CRAN-plyr 
Requires:         R-CRAN-rappdirs 
Requires:         R-CRAN-stringr 
Requires:         R-CRAN-tibble 

%description
Proteins reside in either the cell plasma or in the cell membrane. A
membrane protein goes through the membrane at least once. Given the amino
acid sequence of a membrane protein, the tool 'PureseqTM'
(<https://github.com/PureseqTM/pureseqTM_package>, as described in
"Efficient And Accurate Prediction Of Transmembrane Topology From Amino
acid sequence only.", Wang, Qing, et al (2019), <doi:10.1101/627307>), can
predict the topology of a membrane protein. This package allows one to use
'PureseqTM' from R.

%prep
%setup -q -c -n %{packname}

find -type f -executable -exec grep -Iq . {} \; -exec sed -i -e '$a\' {} \;
[ -d %{packname}/src ] && find %{packname}/src -type f -exec \
  sed -i 's@/usr/bin/strip@/usr/bin/true@g' {} \; || true

%build

%install

mkdir -p %{buildroot}%{rlibdir}
%{_bindir}/R CMD INSTALL -l %{buildroot}%{rlibdir} %{packname}
test -d %{packname}/src && (cd %{packname}/src; rm -f *.o *.so)
rm -f %{buildroot}%{rlibdir}/R.css
find %{buildroot}%{rlibdir} -type f -exec sed -i "s@%{buildroot}@@g" {} \;

%files
%{rlibdir}/%{packname}