在执行以下规则之前,我正在拼命尝试让一个规则下载我的fastq文件。我尝试了很多方法,包括这里建议的:http://ivory.idyll.org/blog/tag/snakemake.html
下面是我的snakemake的简化版本:
######### functions
def read_samplesTable(inputTable):
data = pandas.read_csv(inputTable)
# Verify column names
if not {'run', 'organism', 'name', 'experiment_title', 'cell_line', 'rep', 'study_name', 'library_strategy', 'library_layout', 'study_title'}.issubset(data.columns.values):
raise KeyError("The samples file must contain the following named columns: 'run', 'organism', 'name', 'experiment_title', 'cell_line', 'rep', 'study_name', 'library_strategy', 'library_layout', 'study_title'")
return data
def retrieveName(description):
result = []
for items in description.iteritems():
result.append(items[1].split(":")[0])
return result
######### Variables
input_table = config["samples"]["summaryFile"]
samplesData = read_samplesTable(input_table)
index_single = samplesData['library_layout'] == 'SINGLE - '
samplesData_single = samplesData[index_single]
gsm_single = retrieveName(samplesData_single["experiment_title"])
outputName_single = samplesData_single['name'] + "_" + samplesData_single['run'] + "_" + gsm_single + "_" + samplesData_single['study_name'] + "_" + samplesData_single['cell_line'] + "_" + samplesData_single['rep']
single_samples = outputName_single.tolist()
names_srrID_single = samplesData_single['run']
############ Rule
rule all:
input:
expand("data/single/{singleEndName}.fastq.gz", singleEndName = single_samples)
rule download_fastq_single:
output:
singleFastq = "data/single/{singleEndName}.fastq.gz"
params:
outputdirectory = config["rawdata"]["fastqrootfolder"]
ssridsingle = lambda wildcards: samplesData_single.loc[wildcards.names_srrID_single, "run"]
shell:
"fastq-dump --accession {params.srridsingle} --defline-seq '@$sn[_$rn]/$ri' --defline-qual \'+\' --gzip --outdir {params.outputdirectory}"规则在一个单独的文件'download-fastq-snakefile‘中,我得到了错误SyntaxError in line 6 of download-fastq-snakefile。
正如我所料,问题来自ssridsingle = lambda wildcards: samplesData_single.loc[wildcards.names_srrID_single, "run"]行
如果你能帮我,那就太好了!
谢谢
发布于 2020-03-17 21:48:26
我猜问题只是缺少了一个逗号:
params:
outputdirectory = config["rawdata"]["fastqrootfolder"], <-- add this comma
ssridsingle = lambda wildcards: samplesData_single.loc[wildcards.names_srrID_single, "run"] 发布于 2020-03-18 04:49:33
是的,这是第一个问题,谢谢!
对于第二个问题,我必须修改对srr id的访问,如下所示:
rule download_fastq_single:
output:
singleFastq = "data/single/{singleEndName}.fastq.gz"
params:
outputdirectory = config["rawdata"]["fastqrootfolder"],
ssridsingle = lambda wildcards: names_srrID_single
shell:
"fastq-dump --accession {params.ssridsingle} --defline-seq '@$sn[_$rn]/$ri' --defline-qual \'+\' --gzip --outdir {params.outputdirectory}"https://stackoverflow.com/questions/60720998
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