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continuous_integration.yml
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name: CI
on:
push:
branches:
- dev
pull_request:
workflow_dispatch:
jobs:
build_and_publish_image:
name: Build and Publish Image
runs-on: ubuntu-latest
steps:
- uses: actions/checkout@v3
with:
token: ${{ secrets.GH_TOKEN }}
- name: Set up Docker Buildx
uses: docker/setup-buildx-action@v2
- name: Docker meta
id: meta
uses: docker/metadata-action@v4
with:
images: pgc-images.sbgenomics.com/d3b-bixu/open-pedcan
tags: |
type=raw,value=analysisjob
# Only tag the image with latest if we're building on the default
# branch (e.g., dev).
type=raw,value=latest,enable={{is_default_branch}}
- name: Login to DockerHub
uses: docker/login-action@v2
with:
registry: pgc-images.sbgenomics.com
username: ${{ secrets.DOCKER_HUB_USERNAME }}
password: ${{ secrets.DOCKER_HUB_ACCESS_TOKEN }}
- name: Build and push
uses: docker/build-push-action@v3
with:
context: .
push: true
tags: ${{ steps.meta.outputs.tags }}
cache-from: type=gha
cache-to: type=gha,mode=max
build-args: github_pat=${{ secrets.GITHUB_TOKEN }}
run_analysis:
name: Run Analysis
needs: build_and_publish_image
runs-on: ubuntu-latest
strategy:
fail-fast: false
matrix:
include:
# Molecular subtyping modules
- name: Molecular Subtyping - MB
entrypoint: molecular-subtyping-MB/run-molecular-subtyping-mb.sh
openpbta_subset: 0
- name: Molecular Subtyping - CRANIO
entrypoint: molecular-subtyping-CRANIO/run-molecular-subtyping-cranio.sh
openpbta_subset: 0
- name: Molecular Subtyping - EPN
entrypoint: molecular-subtyping-EPN/run-molecular-subtyping-EPN.sh
- name: Molecular Subtyping - EMBRYONAL
entrypoint: molecular-subtyping-embryonal/run-embryonal-subtyping.sh
openpbta_testing: 1
- name: Molecular Subtyping - CHORDOMA
entrypoint: molecular-subtyping-chordoma/run-molecular-subtyping-chordoma.sh
openpbta_subset: 0
- name: Molecular Subtyping - EWS
entrypoint: molecular-subtyping-EWS/run_subtyping.sh
- name: Molecular Subtyping - NEUROCYTOMA
entrypoint: molecular-subtyping-neurocytoma/run_subtyping.sh
- name: Molecular Subtyping - HGG
entrypoint: molecular-subtyping-HGG/run-molecular-subtyping-HGG.sh
- name: Molecular Subtyping - LGG
entrypoint: molecular-subtyping-LGAT/run_subtyping.sh
openpbta_subset: 0
- name: Molecular Subtyping - NBL
entrypoint: molecular-subtyping-NBL/run-molecular-subtyping-NBL.sh
- name: Molecular Subtyping - PATHOLOGY/COMPILE
entrypoint: molecular-subtyping-pathology/run-subtyping-aggregation.sh
openpbta_testing: 1
- name: Molecular Subtyping - INTEGRATE (+ add cancer groups)
entrypoint: molecular-subtyping-integrate/run-subtyping-integrate.sh
- name: Molecular Subtyping - ATRT
entrypoint: molecular-subtyping-ATRT/run-molecular-subtyping-ATRT.sh
# Analysis modules
- name: Independent Specimens
entrypoint: independent-samples/run-independent-samples.sh
- name: Independent Specimens pre-release
entrypoint: independent-samples/run-independent-samples.sh
run_for_subtyping: 1
- name: TP53/NF1 scores
entrypoint: tp53_nf1_score/run_classifier.sh
openpedcan_polya_strand: 0
- name: Fusion filtering
entrypoint: fusion_filtering/run_fusion_merged.sh
- name: Fusion summary
entrypoint: fusion-summary/run-new-analysis.sh
openpbta_subset: 0
- name: Consensus CN Manta
entrypoint: copy_number_consensus_call_manta/run_consensus_call.sh
- name: Consensus CN
entrypoint: copy_number_consensus_call/run_consensus_call.sh
- name: Consensus CN annotation
entrypoint: focal-cn-file-preparation/run-prepare-cn.sh
openpbta_testing: 1
- name: TMB calculation
entrypoint: tmb-calculation/run_tmb_calculation.sh
#- name: Immune Deconvolution
# entrypoint: immune-deconv/run-immune-deconv.sh
#- name: EFO/MONDO annotation
# entrypoint: efo-mondo-mapping/run_search_and_qc.sh
- name: ENSEMBL Gene matching
entrypoint: gene_match/run-gene-mapping.sh
#- name: Update table annotation data
# entrypoint: long-format-table-utils/run-update-long-format-table-utils.sh
- name: RNA-Seq Expression Summary stats
entrypoint: rna-seq-expression-summary-stats/run-rna-seq-expression-summary-stats.sh
# MTP-specific modules
- name: Fusion frequency tables
entrypoint: fusion-frequencies/run-frequencies.sh
- name: SNV frequency tables
entrypoint: snv-frequencies/run-snv-frequencies.sh
- name: CNV frequency tables
entrypoint: cnv-frequencies/run-cnv-frequencies-analysis.sh
- name: RNA-Seq batch correction
entrypoint: rnaseq-batch-correct/run_ruvseq.sh
steps:
- uses: actions/checkout@v3
- name: Download Data
uses: docker://pgc-images.sbgenomics.com/d3b-bixu/open-pedcan:analysisjob
with:
entrypoint: ./download-data.sh
env:
OPENPEDCAN_URL: https://s3.amazonaws.com/d3b-openaccess-us-east-1-prd-pbta/open-targets
OPENPEDCAN_RELEASE: testing
- name: Run Analysis
uses: docker://pgc-images.sbgenomics.com/d3b-bixu/open-pedcan:analysisjob
with:
entrypoint: analyses/${{ matrix.entrypoint }}
env:
OPENPBTA_SUBSET: ${{ matrix.openpbta_subset }}
OPENPBTA_TESTING: ${{ matrix.openpbta_testing }}
RUN_FOR_SUBTYPING: ${{ matrix.run_for_subtyping }}
OPENPEDCAN_POLYA_STRAND: ${{ matrix.openpedcan_polya_strand }}