流程管理工具snakemake学习笔记杂记

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发布于 2022-05-23 15:53:03

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发布于 2022-05-23 15:53:03

文章被收录于专栏：小明的数据分析笔记本

snakemake学习笔记001：使用fastp对原始数据过滤

参考

1 https://www.jianshu.com/p/14b9eccc0c0e
2 https://stackoverflow.com/questions/56271154/use-snakemake-pair-end-bwa-alignment
3 https://bioinformaticsonline.com/snippets/view/43590/rules-to-run-fastp-snakemake
4 https://xizhihui.github.io/2018/10/28/%E6%B5%81%E7%A8%8B%E6%9E%84%E5%BB%BA-Snakemake%E4%BD%BF%E7%94%A8%E5%88%9D%E6%AD%A5/
5 https://www.youtube.com/watch?v=_wUGzqEjg6A&t=996s
6 https://www.youtube.com/watch?v=Bdxh0fSBOSA
7 https://www.youtube.com/watch?v=aZ0QlqtR2KM&t=279s

import os
import glob

input_folder = "/home/myan/scratch/private/pome_WGS/huoyan_14_variety/"
output_folder = "/home/myan/scratch/private/practice_data/snakemake/20220412/fastp.results/"

SRA,FRR = glob_wildcards(input_folder+"{sra}_{frr}.fq.gz")

rule all:
    input:
        expand(output_folder+"{sra}.html",sra=SRA),
        expand(output_folder+"{sra}.json",sra=SRA)


rule fastp:
    input:
        read01 = input_folder + "{sra}_1.fq.gz",
        read02 = input_folder + "{sra}_2.fq.gz"
    output:
        read01 = output_folder + "{sra}_1.clean.fq.gz",
        read02 = output_folder + "{sra}_2.clean.fq.gz",
        html = output_folder + "{sra}.html",
        json = output_folder + "{sra}.json"
    threads:
        8
    shell:
        """
        fastp -i {input.read01} -I {input.read02} -o {output.read01} -O {output.read02} --thread {threads} --html {output.html} --json {output.json}
        """

这里rule all的作用还是没有搞明白，看有的文档说是最终保留的文件，我这里rule all 只写了了最终的html和json，但是最终的结果里是有过滤后的fastq文件的

还有好多基础知识需要看

路径里的文件夹如果不存在会新建一个文件夹

snakemake学习笔记002：hisat2+samtools+stringtie流程转录组分析

今天的内容增加了config文件

input_folder:
    "/home/myan/scratch/private/practice_data/RNAseq/chrX_data/"
output_folder:
    "/home/myan/scratch/private/practice_data/RNAseq/snakemake.rnaseq/"

index_folder:
    "/mnt/shared/scratch/myan/private/practice_data/RNAseq/chrX_data/indexes/"

index_name:
    "chrX_tran"

samples_folder:
    "/mnt/shared/scratch/myan/private/practice_data/RNAseq/chrX_data/samples/"

gtf_folder:
    "/mnt/shared/scratch/myan/private/practice_data/RNAseq/chrX_data/genes/chrX.gtf"

config文件主要用来指定文件的存贮路径

snakemake文件的内容

configfile: "config.yaml"

import os
import glob
print(config)
print(config['input_folder'])
print(config['output_folder'])

SRR,FRR = glob_wildcards(config['samples_folder']+"{srr}_chrX_{frr}.fastq.gz")

rule all:
    input:
        expand(config["output_folder"] + "output.sam/{srr}.sam",srr=SRR),
        expand(config['output_folder'] + "output.bam/{srr}.bam",srr=SRR),
        expand(config['output_folder'] + "output.gtf/{srr}.gtf",srr=SRR)

rule hisat2:
    input:
        read01 = config['samples_folder'] + "{srr}_chrX_1.fastq.gz",
        read02 = config['samples_folder'] + "{srr}_chrX_2.fastq.gz",

    output:
        sam = config['output_folder'] + "output.sam/{srr}.sam"
    threads:
        8
    params:
        index_file = config['index_folder']+config['index_name']
    shell:
        """
        hisat2 -p {threads} --dta -x {params.index_file} -1 {input.read01} -2 {input.read02} -S {output.sam}
        """

rule samtools:
    input:
        sam = rules.hisat2.output.sam
    output:
        bam = config['output_folder'] + "output.bam/{srr}.bam"
    threads:
        8
    shell:
        """
        samtools sort -@ {threads} -o {output.bam} {input.sam}
        """

rule stringtie:
    input:
        gtf = config['gtf_folder'],
        bam = rules.samtools.output.bam
    output:
        gtf = config['output_folder'] + "output.gtf/{srr}.gtf"
    params:
        l = "{srr}"
    threads:
        8
    shell:
        """
        stringtie -p {threads} -G {input.gtf} -o {output.gtf} -l {params.l} {input.bam}
        """

后面转录本定量的步骤还没有写完，好像还可以把差异表达分析的脚本嵌入进来

未完待续

示例数据用到的是论文

Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie, and Ballgown

中的数据

snakemake学习笔记003：stringtie合并转录本

SRR, = glob_wildcards("output.gtf/"+"{srr}.gtf")
#SRR = ["ERR188401","ERR204916"]
#rule all:
#    input:
#        expand("output.gtf/"+"{srr}.gtf",srr=SRR),

rule gtflist:
    input:
        gtffiles = expand("output.gtf/"+"{srr}.gtf",srr=SRR)
    output:
        output_txt = "MergedList.txt"
    run:
        with open(output.output_txt,'w') as f:
            for gtf in input.gtffiles:
                print(gtf,file=f)

第一行SRR后面有一个逗号

最开始没写这个逗号，一直遇到报错

image.png

Building DAG of jobs... MissingInputException in line 3 of /mnt/shared/scratch/myan/private/practice_data/RNAseq/snakemake.rnaseq/gtf_list.py: Missing input files for rule all: output.gtf/['ERR188337', 'ERR188245', 'ERR188428', 'ERR188401', 'ERR204916', 'ERR188383', 'ERR188104', 'ERR188257', 'ERR188273', 'ERR188044', 'ERR188234', 'ERR188454'].gtf

snakemake学习笔记004:前后两个rule为啥连不起来呢？

SRR, = glob_wildcards("output.gtf/"+"{srr}.gtf")
#SRR = ["ERR188401","ERR204916"]
rule all:
    input:
        #expand("output.gtf/"+"{srr}.gtf",srr=SRR),
        "MergedList.txt",

rule gtflist:
    input:
        gtffiles = expand("output.gtf/"+"{srr}.gtf",srr=SRR)
    output:
        output_txt = "MergedList.txt"
    run:
        with open(output.output_txt,'w') as f:
            for gtf in input.gtffiles:
                print(gtf,file=f)



rule stringtieMerge:
    input:
        refgtf = "/mnt/shared/scratch/myan/private/practice_data/RNAseq/chrX_data/genes/chrX.gtf",
        gtflist = "MergedList.txt"
    output:
        gtf = "output.merged.gtf/StringtieMerged.gtf"
    log:
        "output.merged.gtf/StringtieMerge.logs"
    threads:
        1
    params:
        "-m 200 -c 3"
    shell:
        """
        stringtie --merge {params} -p {threads} -G {input.refgtf} -o {output.gtf} {input.gtflist}
        """

第二个rule就是不运行

原来是在rule all 代码里少写了第二个rule的输出文件

正确写法是

SRR, = glob_wildcards("output.gtf/"+"{srr}.gtf")
#SRR = ["ERR188401","ERR204916"]
rule all:
    input:
        #expand("output.gtf/"+"{srr}.gtf",srr=SRR),
        "MergedList.txt",
        "output.merged.gtf/StringtieMerged.gtf"

rule gtflist:
    input:
        gtffiles = expand("output.gtf/"+"{srr}.gtf",srr=SRR)
    output:
        output_txt = "MergedList.txt"
    run:
        with open(output.output_txt,'w') as f:
            for gtf in input.gtffiles:
                print(gtf,file=f)



rule stringtieMerge:
    input:
        refgtf = "/mnt/shared/scratch/myan/private/practice_data/RNAseq/chrX_data/genes/chrX.gtf",
        gtflist = "MergedList.txt"
    output:
        gtf = "output.merged.gtf/StringtieMerged.gtf"
    log:
        "output.merged.gtf/StringtieMerge.logs"
    threads:
        1
    params:
        "-m 200 -c 3"
    shell:
        """
        stringtie --merge {params} -p {threads} -G {input.refgtf} -o {output.gtf} {input.gtflist}
        """

rule all 的作用是啥我还是不懂

snakemake学习笔记005：流程里使用R脚本

rule useRscriptinsnakemake:
    input:
        ballgown_folder = "ballgown",
        pheno = "geuvadis_phenodata.csv"
    output:
        rdat = "bg_chrX_1.Rdata"
    #conda:
        #"envs/ballgown.yaml"
    script:
        "scripts/ballgown_1.R"

尝试嵌入conda的时候遇到报错，暂时不知道是什么原因我的ballgown.yaml文件

name: rnaseq_pra
channels:
  - conda-forge
  - biocondas
dependencies:
  - r=4.0=r40hd8ed1ab_1004
  - bioconductor-ballgown=2.22.0=r40hdfd78af_1

我的ballgown_1.R文件

library(ballgown)
library(genefilter)

pheno_data = read.csv(snakemake@input[["pheno"]])
bg_chrX = ballgown(dataDir = snakemake@input[["ballgown_folder"]],samplePattern = "ERR",pData = pheno_data)
bg_chrX_filt = subset(bg_chrX,"rowVars(texpr(bg_chrX)) > 1",genomesubset=TRUE)
results_transcripts = stattest(bg_chrX_filt,feature="transcript",covariate="sex",adjustvars=c("population"),getFC=TRUE,meas="FPKM")
save(bg_chrX,results_transcripts,file=snakemake@output[["rdat"]])

这里有一个问题是snakemake流程里怎么样使用已经存在的conda环境，看这个流程的时候 https://github.com/Alipe2021/NLncCirSmk/blob/master/NLncCirSmk.smk

他的写法是

rule Part06_CircRNA_Analysis_06_Bam2Anchors:
    input:
        bam = OUTPUTDIR + "./CircRNA/05.UnmappedBam/{sample}.unmapped.bam",
        bai = OUTPUTDIR + "./CircRNA/05.UnmappedBam/{sample}.unmapped.bai"
    output:
        fq = OUTPUTDIR + "./CircRNA/06.Bam2Anchors/{sample}/unmapped_anchors.fq.gz"
    params:
        DIR = OUTPUTDIR + "./CircRNA/06.Bam2Anchors/{sample}"
    run:
        import os
        import subprocess
        if not os.path.exists(params.DIR):
            os.makedirs(params.DIR)

        cmd = ("source activate find_circ_env && unmapped2anchors.py {bam} | "
        " gzip > {fq} && conda deactivate").format(bam=input.bam, fq=output.fq)

        print(cmd)
        subprocess.call(cmd, shell=True)

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原始发表：2022-05-06，如有侵权请联系 cloudcommunity@tencent.com 删除

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