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|
#!/usr/bin/make -f
export DH_VERBOSE=1
pkg := subread
mandir := $(CURDIR)/debian/$(pkg)/usr/share/man/man1
bindir := $(CURDIR)/bin
utildir := $(CURDIR)/bin/utilities
export DEB_BUILD_MAINT_OPTIONS = hardening=+all
include /usr/share/dpkg/architecture.mk
ifeq ($(origin CC),default)
CC = $(DEB_HOST_GNU_TYPE)-gcc
endif
DEB_HOST_ARCH ?= $(shell dpkg-architecture -qDEB_HOST_ARCH)
ifeq ($(DEB_HOST_ARCH),$(filter $(DEB_HOST_ARCH),amd64 i386))
CFLAGS += -mtune=generic -msse3
endif
ifeq ($(DEB_HOST_ARCH_OS), kfreebsd)
CFLAGS += -D KFREEBSD
endif
%:
dh $@
override_dh_clean:
cd src; make -f Makefile.Linux clean
dh_clean
override_dh_auto_build:
cd src; make -f Makefile.Linux
dh_auto_build -- CC=$(CC)
override_dh_auto_test:
ifeq (,$(filter nocheck,$(DEB_BUILD_OPTIONS)))
debian/tests/subread-tests $(CURDIR)
endif
HELP2MAN = help2man --no-info --help-option="''" --no-discard-stderr
override_dh_auto_install:
#fix for gzip-file-is-not-multi-arch-same-safe
find $(CURDIR) -name "*.gz" -exec bash -c 'name="{}"; gzip -d "{}"; gzip -n "$${name%.*}"' \;
mkdir -p $(mandir)
$(HELP2MAN) --name='an accurate and efficient aligner for mapping both genomic \
DNA-seq reads and RNA-seq reads (for the purpose of expression analysis)' \
$(bindir)/subread-align | debian/filter.pl > $(mandir)/subread-align.1;
$(HELP2MAN) --name='builds an base-space or color-space index using the reference sequences' \
$(bindir)/subread-buildindex | debian/filter.pl > $(mandir)/subread-buildindex.1;
$(HELP2MAN) --name='an RNA-seq aligner suitable for all purposes of RNA-seq analyses' \
$(bindir)/subjunc | debian/filter.pl > $(mandir)/subjunc.1;
$(HELP2MAN) --name='a highly efficient and accurate read summarization program' \
$(bindir)/featureCounts | debian/filter.pl > $(mandir)/featureCounts.1;
$(HELP2MAN) --name='a SNP caller that discovers SNPs by testing signals against local background noises' \
$(bindir)/exactSNP | debian/filter.pl > $(mandir)/exactSNP.1;
$(HELP2MAN) --name='detect short and long indels' \
$(bindir)/subindel | debian/filter.pl > $(mandir)/subindel.1;
$(HELP2MAN) --name='long-read aligner that is designed based on seed-and-vote' \
$(bindir)/sublong| debian/filter.pl > $(mandir)/sublong.1;
$(HELP2MAN) --name='scans the entire genome and reports all matches of a specified sequence' \
$(utildir)/subread-fullscan | debian/filter.pl > $(mandir)/subread-fullscan.1;
# $(HELP2MAN) --name='counting the coverage of mapped reads at each location on the entire reference genome' \
# $(utildir)/coverageCount | debian/filter.pl > $(mandir)/coverageCount.1;
# $(HELP2MAN) --name='detectionCall' \
# $(utildir)/detectionCall | debian/filter.pl > $(mandir)/detectionCall.1;
$(HELP2MAN) --name='calculate the proportion of mapped reads/fragments' \
$(utildir)/propmapped | debian/filter.pl > $(mandir)/propmapped.1;
$(HELP2MAN) --name='retrieve Phred score for read bases' \
$(utildir)/qualityScores| debian/filter.pl > $(mandir)/qualityScores.1;
$(HELP2MAN) --name='Find reads that are from the same pair in the input and then place them next \
to each other in the output. A dummy read is added for each singleton read that does not have a pair. \
The output file is compatible with featureCounts program' \
$(utildir)/repair| debian/filter.pl > $(mandir)/repair.1;
$(HELP2MAN) --name='Remove duplicated reads' \
$(utildir)/removeDup| debian/filter.pl > $(mandir)/removeDup.1;
$(HELP2MAN) --name='Flatten features included in a GTF annotation and save the modified annotation \
to a SAF format file.' \
$(utildir)/flattenGTF| debian/filter.pl > $(mandir)/flattenGTF.1;
dh_auto_install
override_dh_installexamples-indep:
tar --sort=name \
--mtime="@${SOURCE_DATE_EPOCH}" \
--owner=root --group=root --numeric-owner \
--mode=go=rX,u+rw,a-s \
-cJf $(CURDIR)/debian/subread-data/usr/share/doc/subread/examples/test.tar.xz test/
|
