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$TACC_HTSEQ_DIR/scripts/htseq-count -m intersection-nonempty --stranded reverse -i gene_id C1_R1_thout/accepted_hits.sam reference/genes.formatted.gtf > C1_count1.gff $TACC_HTSEQ_DIR/scripts/htseq-count -m intersection-nonempty --stranded reverse -i gene_id C1_R2_thout/accepted_hits.sam reference/genes.formatted.gtf > C1_count2.gff $TACC_HTSEQ_DIR/scripts/htseq-count -m intersection-nonempty --stranded reverse -i gene_id C1_R3_thout/accepted_hits.sam reference/genes.formatted.gtf > C1_count3.gff $TACC_HTSEQ_DIR/scripts/htseq-count -m intersection-nonempty --stranded reverse -i gene_id C2_R1_thout/accepted_hits.sam reference/genes.formatted.gtf > C2_count4.gff $TACC_HTSEQ_DIR/scripts/htseq-count -m intersection-nonempty --stranded reverse -i gene_id C2_R2_thout/accepted_hits.sam reference/genes.formatted.gtf > C2_count5.gff $TACC_HTSEQ_DIR/scripts/htseq-count -m intersection-nonempty --stranded reverse -i gene_id C2_R3_thout/accepted_hits.sam reference/genes.formatted.gtf > C2_count6.gff join C1_count1.gff C1_count2.gff| join - C1_count3.gff | join - C2_count4.gff |join - C2_count5.gff|join - C2_count6.gff > gene_counts_HTseq.gff #if you have many samples, use for-loop and join |
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