Workflows

What is a Workflow?
738 Workflows visible to you, out of a total of 793

This workflow take as input a collection of paired fastq. Remove adapters with cutadapt, map pairs with bowtie2 allowing dovetail. Keep MAPQ30 and concordant pairs. BAM to BED. MACS2 with "ATAC" parameters.

Type: Galaxy

Creators: Lucille Delisle, Lucille Delisle

Submitter: WorkflowHub Bot

This workflow take as input a collection of paired fastq. It uses HiCUP to go from fastq to validPair file. The pairs are filtered for MAPQ and sorted by cooler to generate a tabix dataset. Cooler is used to generate a balanced cool file to the desired resolution.

Type: Galaxy

Creator: Lucille Delisle

Submitter: WorkflowHub Bot

Stable

TronFlow BAM preprocessing pipeline

GitHub tag (latest SemVer) Automated tests DOI ...

Type: Nextflow

Creators: None

Submitter: Pablo Riesgo Ferreiro

Stable

TronFlow alignment pipeline

GitHub tag (latest SemVer) Run tests DOI ...

Type: Nextflow

Creators: None

Submitter: Pablo Riesgo Ferreiro

Stable

CoVigator logo

CoVigator pipeline: variant detection pipeline for Sars-CoV-2

DOI Run tests [![Powered by ...

Type: Nextflow

Creators: Pablo Riesgo Ferreiro, Thomas Bukur, Patrick Sorn

Submitter: Pablo Riesgo Ferreiro

This workflow take as input a collection of paired fastq. It will remove bad quality and adapters with cutadapt. Map with Bowtie2 end-to-end. Will remove reads on MT and unconcordant pairs and pairs with mapping quality below 30 and PCR duplicates. Will compute the pile-up on 5' +- 100bp. Will call peaks and count the number of reads falling in the 1kb region centered on the summit. Will plot the number of reads for each fragment length.

Type: Galaxy

Creators: Lucille Delisle, Lucille Delisle

Submitter: WorkflowHub Bot

This workflow takes as input a list of single-read fastqs. Adapters and bad quality bases are removed with cutadapt. Reads are mapped with STAR with ENCODE parameters and genes are counted simultaneously. The counts are reprocess to be similar to HTSeq-count output. FPKM are computed with cufflinks. Coverage (per million mapped reads) are computed with bedtools on uniquely mapped reads.

Type: Galaxy

Creators: Lucille Delisle, Lucille Delisle

Submitter: WorkflowHub Bot

This workflow takes as input a list of paired-end fastqs. Adapters and bad quality bases are removed with cutadapt. Reads are mapped with STAR with ENCODE parameters and genes are counted simultaneously. The counts are reprocess to be similar to HTSeq-count output. FPKM are computed with cufflinks. Coverage (per million mapped reads) are computed with bedtools on uniquely mapped reads (with R2 orientation inverted).

Type: Galaxy

Creators: Lucille Delisle, Lucille Delisle

Submitter: WorkflowHub Bot

Github: https://github.com/Lcornet/GENERA

BCCM GEN-ERA tools repository

Please visit the wiki for tutorials and access to the tools: https://github.com/Lcornet/GENERA/wiki

NEWS

Mantis is now installed in a singularity container for the Metabolic workflow (install is no longer necessary).

Information about the GEN-ERA project

Please visit https://bccm.belspo.be/content/bccm-collections-genomic-era

Publications

  1. ToRQuEMaDA: tool for retrieving queried Eubacteria, metadata and dereplicating ...

Type: Nextflow

Creator: Luc Cornet

Submitter: Luc Cornet

DOI: 10.48546/workflowhub.workflow.416.1

Work-in-progress
No description specified

Type: Common Workflow Language

Creator: Denys Savchenko

Submitter: Volodymyr Savchenko

DOI: 10.48546/workflowhub.workflow.415.1

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