Workflows
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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.
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.
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).
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
- ToRQuEMaDA: tool for retrieving queried Eubacteria, metadata and dereplicating ...
The Regulatory Mendelian Mutation (ReMM) score was created for relevance prediction of non-coding variations (SNVs and small InDels) in the human genome (GRCh37) in terms of Mendelian diseases. This project updates the ReMM score for the genome build GRCh38 and combines GRCh37 and GRCh38 into one workflow.
Pre-requirements
Conda
We use Conda as software and dependency management tool. Conda installation guidelines can be found here:
https://conda.io/projects/conda/en/latest/user-guide/install/index.html ...
Example workflow which allows the use of Mothra
Accepts (e.g.) these input files, bundled as a collection.