%global __brp_check_rpaths %{nil}
%global packname  chromseq
%global packver   0.1.3
%global rlibdir   /usr/local/lib/R/library

Name:             R-CRAN-%{packname}
Version:          0.1.3
Release:          3%{?dist}%{?buildtag}
Summary:          Split Chromosome 'Fasta' File

License:          Artistic-2.0
URL:              https://cran.r-project.org/package=%{packname}
Source0:          %{url}&version=%{packver}#/%{packname}_%{packver}.tar.gz


BuildRequires:    R-devel >= 2.10
Requires:         R-core >= 2.10
BuildArch:        noarch
BuildRequires:    R-utils 
BuildRequires:    R-base 
Requires:         R-utils 
Requires:         R-base 

%description
Chromosome files in the 'Fasta' format usually contain large sequences
like human genome. Sometimes users have to split these chromosomes into
different files according to their chromosome number. The 'chromseq' can
help to handle this. So the selected chromosome sequence can be used for
downstream analysis like motif finding. Howard Y. Chang(2019)
<doi:10.1038/s41587-019-0206-z>.

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

find -type f -executable -exec grep -Iq . {} \; -exec sed -i -e '$a\' {} \;

%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

%files
%{rlibdir}/%{packname}