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Running Batch Jobs
To launch a DNAnexus application or workflow on many files automatically, one may write a short script to loop over the desired files in a project and launch jobs or analyses. Alternatively, the DNAnexus SDK provides a few handy utilities for batch processing. To use the GUI to run in batch mode, see these instructions.
In this tutorial, we'll batch process a series of sample FASTQs (forward and reverse reads). We'll use the
dx generate_batch_inputs command to generate a batch file -- a tab-delimited (TSV) file where each row corresponds to a single run in our batch. Then we'll process our batch using the dx run command with the --batch-tsv options.In the project My Research Project we have the following files in our root directory:
$ dx select "My Research Project"
Selected project My Research Project
$ dx ls /
RP10B_S1_R1_001.fastq.gz
RP10B_S1_R2_001.fastq.gz
RP10T_S5_R1_001.fastq.gz
RP10T_S5_R2_001.fastq.gz
RP15B_S4_R1_002.fastq.gz
RP15B_S4_R2_002.fastq.gz
RP15T_S8_R1_002.fastq.gz
RP15T_S8_R2_002.fastq.gz
We want to batch process these read pairs using BWA-MEM (link requires platform login). For a single execution of the BWA-MEM app, we need to specify the following inputs:
reads_fastqgzs- FASTQ containing the left matesreads2_fastqgzs- FASTQ containing the right matesgenomeindex_targz- BWA reference genome index
We'll use the BWA reference genome index from the public Reference Genome (requires platform login) project for all runs; however, for the forward and reverse reads we want read pairs used to vary from run to run. To generate a batch file that pairs our input reads:
$ dx generate_batch_inputs -ireads_fastqgzs='RP(.*)_R1_(.*).fastq.gz' -ireads2_fastqgzs='RP(.*)_R2_(.*).fastq.gz'
Found 4 valid batch IDs matching desired pattern.
Created batch file dx_batch.0000.tsv
CREATED 1 batch files each with at most 500 batch IDs.
You can optionally provide a
--path argument and provide a specific file and folder to search for recursively within your project. Specifically, the value for --path must be a directory specified as:/path/to/directory or project-xxxx:/path/to/directoryAny file present within this directory or recursively within any subdirectory of this directory will be considered a candidate for a batch run.
The
(.*) are regular expression groups. You can provide arbitrary regular expressions as input. The first match in the group will be the pattern used to group pairs in the batch, these matches are called batch identifiers (batch IDs). To explain this behavior in more detail, We will use the output of the dx generate_batch_inputs command above:The
dx generate_batch_inputs command creates the dx_batch.0000.tsv that looks like:$ cat dx_batch.0000.tsv
batch ID reads_fastqgzs reads2_fastqgzs pair1 ID pair2 ID
10B_S1 RP10B_S1_R1_001.fastq.gz RP10B_S1_R2_001.fastq.gz file-aaa file-bbb
10T_S5 RP10T_S5_R1_001.fastq.gz RP10T_S5_R2_001.fastq.gz file-ccc file-ddd
15B_S4 RP15B_S4_R1_002.fastq.gz RP15B_S4_R2_002.fastq.gz file-eee file-fff
15T_S8 RP15T_S8_R1_002.fastq.gz RP15T_S8_R2_002.fastq.gz file-ggg file-hhh
Recall the regular expression was
RP(.*)_R1_(.*).fastq.gz. Although there are two grouped matches in this example, only the first one is used as the pattern for the batch ID. For example, the pattern identified for RP10B_S1_R1_001.fastq.gz is 10B_S1 which corresponds to the first grouped match while the second one is ignored.Examining the TSV file above, the files are grouped as expected, with the first match labeling the identifier of the group within the batch. The next two columns show the file names. The last two columns contain the IDs of the files on the DNAnexus platform. You can either edit this file directly or import it into a spreadsheet to make any subsequent changes.
Note that if an input for the app is an array, the input file IDs within the batch.tsv file need to be in square brackets in order to work. The following bash command will add brackets to the file IDs to column 4 and 5. You may need to change the variables in the below command ("$4" and "$5") to match the correct columns in your file. The command's output file, "new.tsv", is ready for the
dx run --batch-tsv command.head -n 1 dx_batch.0000.tsv > temp.tsv && tail -n +2 dx_batch.0000.tsv | awk '{sub($4, "[&]"); print}' | awk '{sub($5, "[&]"); print}' >> temp.tsv; tr -d '\r' < temp.tsv > new.tsv; rm temp.tsvNote that the example above is for a case where all files have been paired properly.
dx generate_batch_inputs will create a TSV for all files that can be successfully matched for a particular batch ID. There are two classes of errors for batch IDs that are not successfully matched:- A particular input is missing (e.g.
reads_fastqgzshas a pattern but no corresponding match can be found forreads2_fastqgzs) - More than one file ID matches the exact same name
For both of these cases,
dx generate_batch_inputs returns a description of these errors to STDERR.If you match more than 500 files, multiple batch files will be generated in groups of 500 to limit the number of jobs in a single batch run.
We have our batch file so now we can execute our BWA-MEM batch process:
$ dx run bwa_mem_fastq_read_mapper -igenomeindex_targz="Reference Genome Files":"/H. Sapiens - GRCh38/GRCh38.no_alt_analysis_set.bwa-index.tar.gz" --batch-tsv dx_batch.0000.tsv
# Output
Here,
genomeindex_targz is a parameter set at execution time that is common to all groups in the batch and --batch-tsv corresponds to the input file generated above.To monitor a batch job, simply use the 'Monitor' tab like you normally would for jobs you launch.
In order to direct the output of each run into a separate folder, the
--batch-folders flag can be used, for example:$ dx run bwa_mem_fastq_read_mapper -igenomeindex_targz="project-BQpp3Y804Y0xbyG4GJPQ01xv:file-BFBy4G805pXZKqV1ZVGQ0FG8" --batch-tsv dx_batch.0000.tsv --batch-folders
# Output
This will output the results for each sample in folders named after batch IDs, in our case the folders: "/10B_S1/", "/10T_S5/", "/15B_S4/", and "/15T_S8/". If the folders do not exist, they will be created.
The output folders are created under a path defined with
--destination, which by default is set to current project and the "/" folder. For example, this command will output the result files in "/run_01/10B_S1/", "/run_01/10T_S5/", etc.:$ dx run bwa_mem_fastq_read_mapper -igenomeindex_targz="project-BQpp3Y804Y0xbyG4GJPQ01xv:file-BFBy4G805pXZKqV1ZVGQ0FG8" --batch-tsv dx_batch.0000.tsv --batch-folders --destination=My_project:/run_01
# Output
dx generate_batch_inputs is limited to starting runs that differ only in input fields of type file. Use a more flexible for loop construct if you want batch runs that differ in string, file array or other non-file type inputs.Additionally, a
for loop allows you to specify other dx run arguments such as name for every run: for i in 1 2; do
dx run swiss-army-knife -icmd="wc *>${i}.out" -iin="fileinput_batch${i}a" -iin="file_input_batch${i}b" --name "sak_batch${i}"
done
You can also use the
dx run command in order to use stage_id . For example, if you create a workflow called "Trio Exome Workflow - Jan 1st 2020 9:00am" in your project, you can run it from the command line:dx login
dx run "Trio Exome Workflow - Jan 1st 2020 9\:00am"
Note the
\ that is needed to escape the : in the workflow name.Inputs to the workflow can be specified using
dx run <workflow> --input name=stage_id:value, where stage_id is a numeric ID starting at 0. More help can be found by running the commands dx run --help and dx run <workflow> --help.To batch multiple inputs then, do the following:
dx cd /path/to/inputs
for i in $(dx ls); do
dx run "Trio Exome Workflow - Jan 1st 2020 9\:00am" --input 0.reads="$i"
done
For additional information and examples of how to run batch jobs, Chapter 6 of this reference guide may be useful. Note that this material is not a part of the official DNAnexus documentation and is for reference only.
Last modified 9mo ago