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nextflow
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A DSL for data-driven computational pipelines
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A curated collections of Nextflow implementation patterns -- http://nextflow-io.github.io/patterns/index.html
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Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
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A flexible pipeline for complete analysis of bacterial genomes
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Our VM/Docker sharing infrastructure and management component
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ChIP-seq peak-calling, QC and differential analysis pipeline.
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A graphical user interface for distributed data processing of high throughput genomics
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GATK RNA-Seq Variant Calling in Nextflow
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Methylation (Bisulfite-Sequencing) analysis pipeline using Bismark or bwa-meth + MethylDackel
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16S rRNA amplicon sequencing analysis workflow using QIIME2
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WtP: Phage identification via nextflow and docker or singularity
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RNA-seq analysis pipeline for detection gene-fusions
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Nextflow pipeline for analysis of direct RNA Nanopore reads
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Nextflow RNA-Seq Best Practice analysis pipeline, used at the SciLifeLab National Genomics Infrastructure.
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Aug 20, 2018 - Groovy
ashildv
commented
Jan 7, 2021
Hi there,
I wonder if it would be possible to add a feature in the pipeline allowing libraries made with different adapter sequences to be processed in the same run.
For example, my colleagues and I are often working with a mixture of Illumina and BGI (4 channel) sequencing data and it would be cool to be able run these data together, instead of having to run adapter removal separately for eac
Assembly and binning of metagenomes
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Multi-sample somatic variant caller
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See the main fork of this repository here >>>
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Assembly and intrahost/low-frequency variant calling for viral samples
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It would be nice to add a params to choose the VEP genome assembly.
In most cases it is the
--genomeparams, but I'm assuming it'll be easier to control if we have that as a separate params.For example, it's currently not working with the
--genome customsetting.