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Updated default versions for several tools to the newest version. Pin the
volatile python container to a specific hash digest.
Changes in Cromwell 48 made it impossible to use the wide array of inputs
in our documentation (such as Germline.sampleWorkflow.QC.Cutadapt.minimumLength). Fixes have been made
upstream and in the pipeline. From Cromwell 52 onwards these options are
available again.
WDL files and import zip packages are now offered with every release to
make downloading and running much easier.
The output directory was restructured to contain less nested folders.
Performance has improved as a result of extensive benchmarking and profiling.
Details can be found here.
Added a bwaThreads option to the input. This sets the number of threads used
by the BWA aligner, and is a major influencer of wall clock time.
Use scatter-regions from the chunked-scatter python package as scattering
tool. The old biopet-scatterregions package did not support scattersizes
larger than 2 billion, making it impossible to have the whole human genome in
one scatter.
Use sambamba markdup for marking duplicates with 2 threads which reduces
wall clock time.
Updated default BWA containers. Both bwa and bwakit now contain 0.7.17
and include samtools 1.10 for fast sorting.
Added bcftools stats to the pipeline for variant
statistics. These stats are reported in the MultiQC report.
Tasks were updated to contain the time_minutes runtime attribute and
associated timeMinutes input, describing the maximum time the task will
take to run.
Document the use of cromwell's final_workflow_outputs_dir feature which
makes the germline and somatic pipelines usable on all of Cromwell's
supported backends. Users are encouraged to use this feature. outputDir references are removed from the documentation.
Make the MultiQC task suitable for use with a final_workflow_outputs_dir
so it can be used on all of Cromwell's supported backends.
Restructure the pipeline so variant calling jobs are scheduled more
efficiently.