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May 1, 2012 02:02
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Example makefile for data processing
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# Makefile for sequence analysis | |
D3 = 10229609_627E8AAXX_s_1.barcode.G1366_D3.q20l50.fq | |
D4 = 10229609_627E8AAXX_s_1.barcode.G1300_D4.q20l50.fq | |
T2 = 10229609_627E8AAXX_s_1.barcode.G1393_T2.q20l50.fq | |
DIPLOIDS = $(D3) $(D4) | |
SEQUENCES = $(DIPLOIDS) $(T2) | |
TEST = test.fq | |
.PHONY: all | |
all: called.vcf | |
.PHONY: test | |
test: $(TEST:.fq=.bam) | |
.PHONY: clean | |
clean: index-clean align-clean snp-clean | |
MAXDIFF = 0.04 | |
# number of threads to use in alignment | |
THREADS = 16 | |
# minimum score for bwasw alignment | |
THRESH = 37 | |
# Gmax_109.fa from http://www.plantgdb.org/XGDB/phplib/download.php?GDB=Gm | |
GMAX = Gmax_109.fa | |
INDEX = $(GMAX).bwt | |
.PHONY: index | |
index: $(INDEX) | |
$(INDEX): $(GMAX) | |
bwa index -a bwtsw $< | |
.PRECIOUS: $(INDEX) | |
.PRECIOUS: $(SEQUENCES:.fq=.sai) | |
.PRECIOUS: $(SEQUENCES:.fq=.sam) | |
.PRECIOUS: $(TEST:.fq=.sam) | |
%.sai: %.fq $(INDEX) | |
bwa aln -t $(THREADS) -I $(GMAX) $< > $@ | |
#%.sam: %.sai $(INDEX) | |
# bwa samse -r "@RG\tID:$<\tPL:ILLUMINA" $(GMAX) $< $*.fq > $@ | |
%.sam: %.fq $(INDEX_BWTSW) | |
bwa bwasw -t $(THREADS) -T $(THRESH) $(GMAX) $< > $@ | |
.PRECIOUS: $(SEQUENCES:.fq=.bam) | |
.PRECIOUS: $(TEST:.fq=.bam) | |
# mpileup expects sorted bam files, so sort them here | |
%.bam: %.sam | |
samtools view -b -h -S -u $< | samtools sort - $* | |
%.fai: %.fa | |
samtools faidx $< | |
mv $<.fai $@ | |
snps.bcf: $(DIPLOIDS:.fq=.bam) $(GMAX:.fq=.fai) | |
samtools mpileup -DABSug -f $(GMAX:.fq=.fai) \ | |
$(DIPLOIDS:.fq=.bam) | tee snps.pileup > snps.bcf | |
# -C 50 | |
called.vcf: snps.bcf | |
bcftools view -s samples.samples -t pair -g snps.bcf > called.vcf | |
.PHONY: index-clean | |
index-clean: | |
rm -f *.amb *.ann *.pac *.rpac *.bwt *.rbwt *.sa *.rsa *.fai | |
.PHONY: align-clean | |
align-clean: | |
rm -f *.sam *.bam | |
.PHONY: snp-clean | |
snp-clean: | |
rm -f *.bcf *.vcf *.pileup |
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