58 lines (54 with data), 2.2 kB
{% for rna_type in rna_types %}
rule map_{{ rna_type }}:
input:
{% if loop.index0 == 0 %}
reads='{output_dir}/unmapped/{sample_id}/clean.fa.gz',
{% else %}
reads='{output_dir}/unmapped/{sample_id}/{{ rna_types[loop.index0 - 1] }}.fa.gz',
{% endif %}
{% if rna_type in ['univec', 'rRNA', 'miRNA', 'circRNA'] %}
index=genome_dir + '/index/{{ aligner }}/{{ rna_type }}.1.bt2'
{% elif rna_type == 'spikein' %}
index=config['spikein_dir'] + '/index/{{ aligner }}/{{ rna_type }}.1.bt2'
{% else %}
index=genome_dir + '/rsem_index/{{ aligner }}/{{ rna_type }}.1.bt2'
{% endif %}
output:
unmapped='{output_dir}/unmapped/{sample_id}/{{ rna_type }}.fa.gz',
bam='{output_dir}/tbam/{sample_id}/{{ rna_type }}.bam'
params:
{% if rna_type in ['univec', 'rRNA', 'miRNA', 'circRNA'] %}
index=genome_dir + '/index/{{ aligner }}/{{ rna_type }}'
{% elif rna_type == 'spikein' %}
index=config['spikein_dir'] + '/index/{{ aligner }}/{{ rna_type }}'
{% else %}
index=genome_dir + '/rsem_index/{{ aligner }}/{{ rna_type }}'
{% endif %}
threads:
config['threads_mapping']
shell:
'''pigz -d -c {input.reads} \
| bowtie2 -f -p {threads} --norc --sensitive --no-unal \
--un-gz {output.unmapped} -x {params.index} - -S - \
| samtools view -b -o {output.bam}
'''
{% endfor %}
rule map_other:
input:
{% if (rna_types|length) == 0 %}
reads='{output_dir}/unmapped/{sample_id}/clean.fa.gz',
{% else %}
reads='{output_dir}/unmapped/{sample_id}/{{ rna_types[-1] }}.fa.gz',
{% endif %}
index=genome_dir + '/genome_index/{{ aligner }}/genome.1.bt2'
output:
unmapped='{output_dir}/unmapped/{sample_id}/other.fa.gz',
bam='{output_dir}/gbam/{sample_id}/other.bam'
params:
index=genome_dir + '/genome_index/{{ aligner }}/genome'
shell:
'''pigz -d -c {input.reads} \
| bowtie2 -f -p {threads} --sensitive --no-unal \
--un-gz {output.unmapped} -x {params.index} - -S - \
| samtools view -b -o {output.bam}
'''