以下snakemake代码无法生成multiqc输出,尽管它适用于orther RSeQC工具,包括geneBody_覆盖、连接_饱和和读取_分布(为清晰起见,此处删除)
rule rseqc_cliping_profile:
"""
Run RSeQC on merged bam files
"""
input:
bam = "results/mappings/{smp}_mappings.bam"
output:
pdf3 = "results/rseqc2/{smp}.clipping_profile.R1.pdf",
pdf4 = "results/rseqc2/{smp}.clipping_profile.R2.pdf",
xls = "results/rseqc2/{smp}.clipping_profile.xls"
shell: """
mkdir -p intermediate/rseqc2
# Run clipping_profile.py
clipping_profile.py -i {input.bam} \
-q 30 \
-s PE \
-o intermediate/rseqc2/{wildcards.smp} \
&& cp -f intermediate/rseqc2/{wildcards.smp}.clipping_profile.R1.pdf {output.pdf3} \
&& cp -f intermediate/rseqc2/{wildcards.smp}.clipping_profile.R2.pdf {output.pdf4} \
&& cp -f intermediate/rseqc2/{wildcards.smp}.clipping_profile.xls {output.xls}
"""
你知道我做错了什么吗
中间体/rseqc2中的结果属于以下类型(此处仅限S12):
S12.clipping_profile.r
S12.clipping_profile.R1.pdf
S12.clipping_profile.R2.pdf
S12.clipping_profile.xls
multiqc -f -i "RSeQC" -o intermediate/multiqc_rseqc2 -n multiqc_rseqc2 intermediate/rseqc2
[INFO ] multiqc : This is MultiQC v1.6
[INFO ] multiqc : Template : default
[INFO ] multiqc : Report title: RSeQC
[INFO ] multiqc : Searching 'intermediate/rseqc2'
[WARNING] multiqc : No analysis results found. Cleaning up..
[INFO ] multiqc : MultiQC complete
这不是一个蛇形问题
尽管剪裁配置文件在我的multiqc配置yaml中,但似乎不适合查找用于打印的剪裁配置文件数据
xls文件实际上是变相的tsv文件;将它们重命名为.txt或.tsv并不能提高几率
The MultiQC documentation on RSeQC support表明MultiQC不支持该特定工具(
clipping_profile
),但它确实支持您提到的其他工具相关问题 更多 >
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