#!/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 = $(DEB_HOST_GNU_TYPE)-gcc endif ifeq ($(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 $@ override_dh_clean: cd src; make -f Makefile.Linux clean dh_clean override_dh_auto_clean: dh_auto_clean rm -f test/subread-align/data/test-err-mut-r1.fq.gz test/subread-align/data/test-err-mut-r2.fq.gz rm -rf bin src/longread-one/make.version find . -name "*.o" -delete override_dh_auto_build: cd src; make -f Makefile.Linux dh_auto_build -- CC=$(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; $(HELP2MAN) --name='helper tool from subread suite' \ $(utildir)/genRandomReads| debian/filter.pl > $(mandir)/genRandomReads.1; dh_auto_install override_dh_installexamples-indep: tar --sort=name \ --mtime="@${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/