Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata
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Updated
Feb 17, 2022 - HTML
Multi-sample genome coverage viewer to observe large, coverage-based anomalies alongside annotations and sample metadata
compare sequences to a shared root reference sequence.
Workflow to download, process, and explore microbial RNA-seq data from NCBI SRA
A Reproducible Untargeted Metabolomics Data Processing Pipeline
Nextflow Workshop at Rocky Mountain Genomics HackCon 2018
This is a demo about how to develop and deploy a pipeline using nextflow, scif, a container (Singularity and Docker) and its posterior deployment.
Nextflow Tutorial - Variant Calling Edition
SPEAQeasy: portable LIBD RNA-seq pipeline using Nextflow. Check https://research.libd.org/SPEAQeasy-example/ for an example on how to use this pipeline and analyze the resulting output files.
Nextflow workflow for basic HiC data processing
Excel report from bioinformatics analysis of viral seq data with nf-core/viralrecon and other Nextflow workflows
Working through NextFlow tutorials. See https://github.com/nextflow-io/training
Using uncertainty in multiple sequence alignments for phylogenetic trees and bootstrap support values
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