name: "spaceranger_count" namespace: "mapping" version: "build_main" authors: - name: "Jakub Majercik" roles: - "author" info: role: "Contributor" links: email: "jakub@data-intuitive.com" github: "jakubmajercik" linkedin: "jakubmajercik" organizations: - name: "Data Intuitive" href: "https://www.data-intuitive.com" role: "Bioinformatics Engineer" argument_groups: - name: "Inputs" arguments: - type: "file" name: "--gex_reference" description: "Path of folder containing 10x-compatible reference" info: null example: - "/path/to/refdata-gex-GRCh38-2020-A" must_exist: true create_parent: true required: true direction: "input" multiple: false multiple_sep: ";" - type: "file" name: "--input" description: "Path to a directory containing input FASTQ data. Individual FASTQ\ \ files should follow the naming convention of 10x Genomics:\n[Sample Name]_S[Sample\ \ Number]_L[Lane Number]_[Read Type]_001.fastq.gz\n\nWhere:\n[Sample Name] is\ \ the name assigned during sample preparation/sequencing\nS[Sample Number] is\ \ the sample index (usually S1, S2, etc.)\nL[Lane Number] identifies the sequencing\ \ lane (L001, L002, etc.)\n\n[Read Type] will be one of:\nR1 - Read 1 (contains\ \ the spatial barcode and UMI)\nR2 - Read 2 (contains the actual cDNA sequence)\n\ I1 - Index Read 1 (if applicable)\nI2 - Index Read 2 (if applicable)\n" info: null example: - "/path/to/fastq_folder" must_exist: true create_parent: true required: true direction: "input" multiple: false multiple_sep: ";" - type: "file" name: "--probe_set" description: "CSV file specifying the probe set used" info: null example: - "Visium_Human_Transcriptome_Probe_Set_v2.0_GRCh38-2020-A.csv" must_exist: true create_parent: true required: true direction: "input" multiple: false multiple_sep: ";" - type: "file" name: "--cytaimage" description: "Brightfield image generated by the CytAssist instrument. \nWhen\ \ using CytAssist workflow, either this or --image must be provided.\n" info: null example: - "cyta_image.tif" must_exist: true create_parent: true required: false direction: "input" multiple: false multiple_sep: ";" - type: "file" name: "--image" description: "H&E or fluorescence microscope image in TIFF or JPG format. \nRequired\ \ for standard Visium workflow, optional when using --cytaimage for CytAssist\ \ workflow.\n" info: null example: - "brightfield.tif" must_exist: true create_parent: true required: false direction: "input" multiple: false multiple_sep: ";" - name: "Outputs" arguments: - type: "file" name: "--output" description: "The folder to store the alignment results" info: null example: - "/path/to/output" must_exist: true create_parent: true required: true direction: "output" multiple: false multiple_sep: ";" - name: "Slide Information" arguments: - type: "string" name: "--slide" description: "Visium slide serial number (e.g., 'V10J25-015')" info: null example: - "V10J25-015" required: false direction: "input" multiple: false multiple_sep: ";" - type: "string" name: "--area" description: "Visium capture area identifier (e.g., 'A1')" info: null example: - "A1" required: false direction: "input" multiple: false multiple_sep: ";" - type: "string" name: "--unknown_slide" description: "Use this option if the slide serial number and area were entered\ \ incorrectly on the CytAssist \ninstrument and the correct values are unknown.\ \ Not compatible with --slide, --area, or \n--slide-file options\n" info: null required: false choices: - "visium-1" - "visium-2" - "visium-2-large" - "visium-hd" direction: "input" multiple: false multiple_sep: ";" - type: "file" name: "--slidefile" description: "Slide design file for offline use" info: null example: - "slide_design.gpr" must_exist: true create_parent: true required: false direction: "input" multiple: false multiple_sep: ";" - type: "boolean_true" name: "--override_id" description: "Overrides the slide serial number and capture area provided in the\ \ Cytassist image metadata" info: null direction: "input" - name: "Image Options" arguments: - type: "file" name: "--darkimage" description: "Multi-channel, dark-background fluorescence image" info: null example: - "fluorescence.tif" must_exist: true create_parent: true required: false direction: "input" multiple: false multiple_sep: ";" - type: "file" name: "--colorizedimage" description: "Color image representing pre-colored dark-background fluorescence\ \ images" info: null example: - "colored_fluorescence.tif" must_exist: true create_parent: true required: false direction: "input" multiple: false multiple_sep: ";" - type: "integer" name: "--dapi_index" description: "Index of DAPI channel (1-indexed) of fluorescence image" info: null example: - 1 required: false min: 1 direction: "input" multiple: false multiple_sep: ";" - type: "double" name: "--image_scale" description: "Microns per microscope image pixel" info: null example: - 0.65 required: false min: 0.01 max: 10.0 direction: "input" multiple: false multiple_sep: ";" - type: "boolean" name: "--reorient_images" description: "Whether to rotate and mirror image to align fiducial pattern" info: null default: - true required: false direction: "input" multiple: false multiple_sep: ";" - name: "Processing Options" arguments: - type: "boolean" name: "--create_bam" description: "Enable or disable BAM file generation" info: null default: - true required: true direction: "input" multiple: false multiple_sep: ";" - type: "boolean_true" name: "--nosecondary" description: "Disable secondary analysis (e.g., clustering)" info: null direction: "input" - type: "integer" name: "--r1_length" description: "Hard trim the input Read 1 to this length before analysis" info: null required: false min: 1 direction: "input" multiple: false multiple_sep: ";" - type: "integer" name: "--r2_length" description: "Hard trim the input Read 2 to this length before analysis" info: null required: false min: 1 direction: "input" multiple: false multiple_sep: ";" - type: "boolean" name: "--filter_probes" description: "Whether to filter the probe set using the \"included\" column" info: null default: - true required: false direction: "input" multiple: false multiple_sep: ";" - type: "integer" name: "--custom_bin_size" description: "Bin Visium HD data to specified size in microns (4-100, even values\ \ only) in addition to the standard binning size (2 µm, 8 µm, 16 µm)" info: null required: false min: 4 max: 100 direction: "input" multiple: false multiple_sep: ";" - name: "Input Selection" arguments: - type: "string" name: "--project" description: "Project folder name within mkfastq output" info: null required: false direction: "input" multiple: false multiple_sep: ";" - type: "string" name: "--sample" description: "Prefix of FASTQ filenames to select" info: null required: false direction: "input" multiple: false multiple_sep: ";" - type: "integer" name: "--lanes" description: "Only use FASTQs from selected lanes" info: null example: - 1 - 2 - 3 required: false direction: "input" multiple: true multiple_sep: ";" resources: - type: "bash_script" path: "script.sh" is_executable: true - type: "file" path: "nextflow_labels.config" dest: "nextflow_labels.config" description: "Count gene expression and protein expression reads from a single capture\ \ area." test_resources: - type: "bash_script" path: "test.sh" is_executable: true - type: "file" path: "visium" - type: "file" path: "GRCh38" info: null status: "enabled" scope: image: "public" target: "public" repositories: - type: "github" name: "openpipeline" repo: "openpipelines-bio/openpipeline" tag: "2.1.2" - type: "github" name: "openpipeline_incubator" repo: "openpipelines-bio/openpipeline_incubator" tag: "main" keywords: - "spaceranger" links: repository: "https://github.com/openpipelines-bio/openpipeline_spatial" docker_registry: "ghcr.io" documentation: "https://www.10xgenomics.com/support/software/space-ranger/latest/analysis/running-pipelines/space-ranger-count" runners: - type: "executable" id: "executable" docker_setup_strategy: "ifneedbepullelsecachedbuild" - type: "nextflow" id: "nextflow" directives: tag: "$id" auto: simplifyInput: true simplifyOutput: false transcript: false publish: false config: labels: mem1gb: "memory = 1000000000.B" mem2gb: "memory = 2000000000.B" mem5gb: "memory = 5000000000.B" mem10gb: "memory = 10000000000.B" mem20gb: "memory = 20000000000.B" mem50gb: "memory = 50000000000.B" mem100gb: "memory = 100000000000.B" mem200gb: "memory = 200000000000.B" mem500gb: "memory = 500000000000.B" mem1tb: "memory = 1000000000000.B" mem2tb: "memory = 2000000000000.B" mem5tb: "memory = 5000000000000.B" mem10tb: "memory = 10000000000000.B" mem20tb: "memory = 20000000000000.B" mem50tb: "memory = 50000000000000.B" mem100tb: "memory = 100000000000000.B" mem200tb: "memory = 200000000000000.B" mem500tb: "memory = 500000000000000.B" mem1gib: "memory = 1073741824.B" mem2gib: "memory = 2147483648.B" mem4gib: "memory = 4294967296.B" mem8gib: "memory = 8589934592.B" mem16gib: "memory = 17179869184.B" mem32gib: "memory = 34359738368.B" mem64gib: "memory = 68719476736.B" mem128gib: "memory = 137438953472.B" mem256gib: "memory = 274877906944.B" mem512gib: "memory = 549755813888.B" mem1tib: "memory = 1099511627776.B" mem2tib: "memory = 2199023255552.B" mem4tib: "memory = 4398046511104.B" mem8tib: "memory = 8796093022208.B" mem16tib: "memory = 17592186044416.B" mem32tib: "memory = 35184372088832.B" mem64tib: "memory = 70368744177664.B" mem128tib: "memory = 140737488355328.B" mem256tib: "memory = 281474976710656.B" mem512tib: "memory = 562949953421312.B" cpu1: "cpus = 1" cpu2: "cpus = 2" cpu5: "cpus = 5" cpu10: "cpus = 10" cpu20: "cpus = 20" cpu50: "cpus = 50" cpu100: "cpus = 100" cpu200: "cpus = 200" cpu500: "cpus = 500" cpu1000: "cpus = 1000" script: - "includeConfig(\"nextflow_labels.config\")" debug: false container: "docker" engines: - type: "docker" id: "docker" image: "ghcr.io/data-intuitive/spaceranger:3.1" target_registry: "images.viash-hub.com" target_tag: "build_main" namespace_separator: "/" setup: - type: "docker" run: - "DEBIAN_FRONTEND=noninteractive apt update && \\\napt upgrade -y && apt install\ \ -y procps && rm -rf /var/lib/apt/lists/*\n" entrypoint: [] cmd: null - type: "native" id: "native" build_info: config: "src/mapping/spaceranger_count/config.vsh.yaml" runner: "nextflow" engine: "docker|native" output: "target/nextflow/mapping/spaceranger_count" executable: "target/nextflow/mapping/spaceranger_count/main.nf" viash_version: "0.9.3" git_commit: "6ae6ad193664a12a39c23f20030ebf03d9e886c6" git_remote: "https://github.com/openpipelines-bio/openpipeline_spatial" package_config: name: "openpipeline_spatial" version: "build_main" info: test_resources: - type: "s3" path: "s3://openpipelines-bio/openpipeline_spatial/resources_test" dest: "resources_test" repositories: - type: "github" name: "openpipeline" repo: "openpipelines-bio/openpipeline" tag: "2.1.2" - type: "github" name: "openpipeline_incubator" repo: "openpipelines-bio/openpipeline_incubator" tag: "main" viash_version: "0.9.3" source: "src" target: "target" config_mods: - ".resources += {path: '/src/labels.config', dest: 'nextflow_labels.config'}\n\ .runners[.type == 'nextflow'].config.script := 'includeConfig(\"nextflow_labels.config\"\ )'" - ".engines += { type: \"native\" }" - ".engines[.type == 'docker'].target_registry := 'images.viash-hub.com'" - ".engines[.type == 'docker'].target_tag := 'build_main'" organization: "vsh" links: repository: "https://github.com/openpipelines-bio/openpipeline_spatial" docker_registry: "ghcr.io"