From 193c803f77d60be554f6994028573ed4286787ca Mon Sep 17 00:00:00 2001 From: =?UTF-8?q?Luk=C3=A1=C5=A1=20Krup=C4=8D=C3=ADk?= Date: Tue, 11 Jun 2019 08:49:43 +0200 Subject: [PATCH 1/2] new file: q/Qualimap/Qualimap-2.2.1-intel-2017a-Py-3.6.eb --- .../Qualimap-2.2.1-intel-2017a-Py-3.6.eb | 31 +++++++++++++++++++ 1 file changed, 31 insertions(+) create mode 100644 q/Qualimap/Qualimap-2.2.1-intel-2017a-Py-3.6.eb diff --git a/q/Qualimap/Qualimap-2.2.1-intel-2017a-Py-3.6.eb b/q/Qualimap/Qualimap-2.2.1-intel-2017a-Py-3.6.eb new file mode 100644 index 00000000..bb915908 --- /dev/null +++ b/q/Qualimap/Qualimap-2.2.1-intel-2017a-Py-3.6.eb @@ -0,0 +1,31 @@ +# IT4Innovations 2019 + +easyblock = "Tarball" + +name = 'Qualimap' +version = '2.2.1' +versionsuffix = '-Py-3.6' + +homepage = 'http://qualimap.bioinfo.cipf.es/' +description = """Qualimap 2 is a platform-independent application written in + Java and R that provides both a Graphical User Inteface (GUI) and a command-line + interface to facilitate the quality control of alignment sequencing data and its + derivatives like feature counts.""" + +toolchain = {'name': 'intel', 'version': '2017a'} + +sources = ['qualimap_v%(version)s.zip'] +source_urls = ['https://bitbucket.org/kokonech/qualimap/downloads'] + +dependencies = [ + ('R', '3.5.3', '-Py-3.6'), +] + +modextrapaths = {"PATH": '.'} + +sanity_check_paths = { + 'files': ['qualimap'], + 'dirs': ['lib', 'scripts', 'species'], +} + +moduleclass = 'bio' From 614aacf0a31d96ae3b7d44e8714f62acc8551011 Mon Sep 17 00:00:00 2001 From: =?UTF-8?q?Luk=C3=A1=C5=A1=20Krup=C4=8D=C3=ADk?= Date: Tue, 11 Jun 2019 09:12:12 +0200 Subject: [PATCH 2/2] modified: q/Qt/Qt-4.8.7.eb deleted: "b/bcl2fastq2/\\" --- "b/bcl2fastq2/\\" | 39 --------------------------------------- q/Qt/Qt-4.8.7.eb | 2 +- 2 files changed, 1 insertion(+), 40 deletions(-) delete mode 100644 "b/bcl2fastq2/\\" diff --git "a/b/bcl2fastq2/\\" "b/b/bcl2fastq2/\\" deleted file mode 100644 index 02469ecd..00000000 --- "a/b/bcl2fastq2/\\" +++ /dev/null @@ -1,39 +0,0 @@ -# IT4Innovations 2019 - -easyblock = 'ConfigureMake' - -name = 'bcl2fastq2' -version = '2.20.0' -versionsuffix = '-Py-3.6' - -homepage = 'https://support.illumina.com/sequencing/sequencing_software/bcl2fastq-conversion-software.html' -description = """bcl2fastq Conversion Software both demultiplexes data and converts BCL files generated by - Illumina sequencing systems to standard FASTQ file formats for downstream analysis.""" - -toolchain = {'name': 'intel', 'version': '2017a'} - -source_urls = [ - 'ftp://webdata2:webdata2@ussd-ftp.illumina.com/downloads/software/bcl2fastq/'] -sources = [{ - 'filename': '%(name)s-v2-20-0-tar.zip', - # source file is a .zip that contains a .tar.gz - 'extract_cmd': 'unzip -p %s | tar -xzvf -', -}] - -start_dir = 'src' -configopts = '--force-builddir --with-cmake=cmake ' - -builddependencies = [ - ('CMake', '3.8.1', '', True), -] - -dependencies = [ - ('Py', '3.6', '', True), -] - -sanity_check_paths = { - 'files': ['bin/bcl2fastq'], - 'dirs': ['lib'] -} - -moduleclass = 'bio' diff --git a/q/Qt/Qt-4.8.7.eb b/q/Qt/Qt-4.8.7.eb index cd708a88..2ab73c5a 100644 --- a/q/Qt/Qt-4.8.7.eb +++ b/q/Qt/Qt-4.8.7.eb @@ -13,7 +13,7 @@ source_urls = [ ] sources = ['%(namelower)s-everywhere-opensource-src-%(version)s.tar.gz'] -dependencies = [('GLib', '2.52.0')] +dependencies = [('GLib', '2.57.1')] platform = 'linux-g++-64'