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c27267ad00
Build pipeline: viash-hub.htrnaseq.v0.14.0-pk2tm
Source commit: eeda989650
Source message: Bump version to v0.14.0
150 lines
6.1 KiB
Plaintext
150 lines
6.1 KiB
Plaintext
---
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format: gfm
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---
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```{r setup, include=FALSE}
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project <- yaml::read_yaml("_viash.yaml")
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license <- paste0(project$links$repository, "/blob/main/LICENSE")
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contributing <- paste0(project$links$repository, "/blob/main/CONTRIBUTING.md")
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```
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# HT-RNAseq
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[](https://www.viash-hub.com/packages/`r project$name`)
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[](`r project$links$repository`)
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[](`r license`)
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[](`r project$links$issue_tracker`)
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[![Viash version](https://img.shields.io/badge/Viash-v`r gsub("-", "--", project$viash_version)`-blue.svg)](https://viash.io)
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## Introduction
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`r project$description`
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```{mermaid lang='mermaid'}
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flowchart TB
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subgraph runner [runner]
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direction TB
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subgraph htrnaseq [HT-RNAseq]
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direction LR
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demultiplex[Well demultiplexing]
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map
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report
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eset
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end
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end
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demultiplex --> map --> report --> eset
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class runner container
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class htrnaseq container
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class demultiplex container-inner
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class map container-inner
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class report container-inner
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class eset container-inner
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class demultiplex node
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class map node
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class report node
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class eset node
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```
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## Example usage
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### Test and example data
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If you want to explore this workflow, it's possible to the use data we use as test data: [a DRUGseq dataset](https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE176150) from the [NCBI Sequence Read Archive](https://www.ncbi.nlm.nih.gov/sra). For the unit and integration tests, this data has been (partly) subsampled to reduce the test runtime. We used [seqtk](https://github.com/lh3/seqtk) for this with a seed of 1, e.g.:
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```bash
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seqtk sample -s1 orig/SRR14730302/VH02001614_S8_R1_001.fastq.gz 10000 > 10k/SRR14730302/VH02001614_S8_R1_001.fastq.gz
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```
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This data is available at: `gs://viash-hub-test-data/htrnaseq/v1/`.
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### Run from Viash Hub
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Open [Viash Hub](https://www.viash-hub.com) and browse to the [htrnaseq component](https://www.viash-hub.com/packages/htrnaseq/v0.3.0/components/workflows/htrnaseq). Press the 'Launch' button and follow the instructions.
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We will start an example run loading just one input and using a barcodes fasta file containing only 2 wells.
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In the first step, we add the `local` profile to the list of profiles in order to limit the cpu and memory requirements of the workflow steps:
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In the next step, we provide the paramters as follows:
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- `input_r1`: `gs://viash-hub-test-data/htrnaseq/v1/100k/SRR14730301/VH02001612_S9_R1_001.fastq`
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- `input_r2`: `gs://viash-hub-test-data/htrnaseq/v1/100k/SRR14730301/VH02001612_S9_R2_001.fastq`
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- `genomeDir`: `gs://viash-hub-test-data/htrnaseq/v1/genomeDir/subset/Homo_sapiens/v0.0.3/`
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- `barcodesFasta`: `gs://viash-hub-test-data/htrnaseq/v1/2-wells-with-ids.fasta`
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- `annotation`: `gs://viash-hub-test-data/htrnaseq/v1/genomeDir/gencode.v41.annotation.gtf.gz`
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Please note that both `input_r1` and `input_r2` can take multiple values. This means that one has to press ENTER after pasting the input path.
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Press the 'Launch' button at the end to get the instructions on how to run the workflow from the CLI.
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### Run using NF-Tower / Seqera Cloud
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It's possible to run the workflow directly from [Seqera Cloud](https://cloud.seqera.io). The necessary [Nextflow schema file](https://nextflow-io.github.io/nf-schema/latest/nextflow_schema/nextflow_schema_specification/) has been built and provided with the workflows in order to use the form-based input. However, Seqera Cloud can not deal with multiple-value parameters when using the form-based input. Therefore, it's better to use Viash Hub also here:
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First, select the option to run the workflow using Seqera Cloud. You will need to create an API token for your account. Once this token is filled in in the corresponding field, you will get the option to select a 'Workspace' and a 'Compute environment'.
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Next, we need to fill in the parameters for the run. This is similar to before:
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In the next screen, pressing the 'Launch' button will actually start the workflow on Seqera Cloud. A message is shown when the submit was successful.
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### Run from the CLI
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Running from the CLI directly without using Viash hub is possible. The easiest is to just use the integrated help functionality, for instance using the following:
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```bash
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nextflow run https://packages.viash-hub.com/vsh/htrnaseq.git \
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-revision v0.8.1 \
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-main-script target/nextflow/workflows/runner/main.nf \
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--help
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```
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### (Optional) Resource usage tuning
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Nextflow's labels can be used to specify the amount of resources a process can use. This workflow uses the following labels for CPU and memory:
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* `verylowmem`, `lowmem`, `midmem`, `highmem`
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* `verylowcpu`, `lowcpu`, `midcpu`, `highcpu`
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The defaults for these labels can be found at `src/config/labels.config`. Nextflow checks that the specified resources for a process do not exceed what is available on the machine and will not start if it does. Create your own config file to tune the labels to your needs, for example:
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```
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// Resource labels
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withLabel: verylowcpu { cpus = 2 }
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withLabel: lowcpu { cpus = 8 }
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withLabel: midcpu { cpus = 16 }
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withLabel: highcpu { cpus = 32 }
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withLabel: verylowmem { memory = { get_memory( 4.GB * task.attempt ) } }
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withLabel: lowmem { memory = { get_memory( 8.GB * task.attempt ) } }
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withLabel: midmem { memory = { get_memory( 16.GB * task.attempt ) } }
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withLabel: highmem { memory = { get_memory( 64.GB * task.attempt ) } }
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```
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When starting nextflow using the CLI, you can use `-c` to provide the file to nextflow and overwrite the defaults.
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## Contributions
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Developed in collaboration with Data Intuitive and Open Analytics.
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Other contributions are welcome.
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