scatter-gather multiple paired-end alignment (bwa)

NicoBxl

Hi,

I've a bunch of samples that are described for now in a json like the one below. Each samples is split in multiple R1-R2 fastq pairs i.e. one pair per sequencing lane. I want to align each lane separately and add an RG tag. Than merge all lanes in one merge bam file. What will be the best way to do that using wdl. I already wrote the different tasks for alignment and sam to bam. And the downstream analysis using the merged bam (markduplicates, base quality recalibration, etc..). So some help to bridge the gap woul be great!

Thank you

{
    "sample": [
        {
        "sample_name": "Sample_1",
        "reads":[
            {
                "R1": "S1_l1_R1.fastq.gz",
                "R2": "S1_l1_R2.fastq.gz",
                "lane": "l1"
            },
            {
                "R1": "S1_l2_R1.fastq.gz",
                "R2": "S1_l2_R2.fastq.gz",
                "lane": "l2"
            },
            {
                "R1": "S1_l3_R1.fastq.gz",
                "R2": "S1_l3_R2.fastq.gz",
                "lane": "l3"
            }
            ]
        },
        {
        "sample_name": "Sample_2",
        "reads":[
            {
                "R1": "S2_l1_R1.fastq.gz",
                "R2": "S2_l1_R2.fastq.gz",
                "lane": "l1"
            },
            {
                "R1": "S2_l2_R1.fastq.gz",
                "R2": "S2_l2_R2.fastq.gz",
                "lane": "l2"
            },
            {
                "R1": "S3_l3_R1.fastq.gz",
                "R2": "S3_l3_R2.fastq.gz",
                "lane": "l3"
            }
            ]
        }]
}

NicoBxl

Here's a figure to explain what I want to do :

oskarv

You might be looking for the batch function for cromwell, with it you can submit several different jobs with one command. I've never used it myself so I cannot show how to do it, but hopefully the documentation is helpful: http://cromwell.readthedocs.io/en/develop/api/RESTAPI/#submit-a-batch-of-workflows-for-execution

I also want to toot my own horn and suggest that you can perhaps use my pipeline as inspiration for your solution, it definitely cannot handle exactly what you want, but there's an easy way of defining the input files and creating the scatter gather operation.
To begin with, here's the repository with the code: https://github.com/oskarvid/wdl_germline_pipeline/

Take a look at the sample input file here: https://github.com/oskarvid/wdl_germline_pipeline/blob/master/intervals/template_sample_manifest.tsv
I've pasted the relevant line below:

SAMPLE FLOWCELL LANE FILE1 FILE2 LIBRARY PLATFORM
sample01 H7LJGBBXX 1 /wdl_pipeline/data/test_R1.fastq.gz /wdl_pipeline/data/test_R2.fastq.gz LIB1 ILLUMINA

As you can see you define the read group and file paths in this file, and if you look at the scatter code here: https://github.com/oskarvid/wdl_germline_pipeline/blob/master/germlinevarcall.wdl#L49 you'll understand how the read group information in the sample file is used in the wdl script. But the pipeline isn't designed to handle multiple samples, only multiple input files for one sample, so it doesn't do everything you want it to. And I think that if you want to be able to handle multiple samples, you'll be better off using the batch execution function.