Tag: Singularity
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No More Command-Line Only: Run Jupyter Lab, RStudio, and VS Code Interactively in Your Browser on Any HPC Cluster with Pixi
This tutorial is contributed by Giang Nguyen, founder of G Labs, providing consulting, software development, infrastructure engineering, and bioinformatics services to support scalable research and production workflows. He helps teams design, build, and optimize cloud/HPC platforms, develop custom tools and pipelines, and deliver reproducible, production-ready solutions for data-intensive science. You have your scRNA-seq environment set…
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Build Once, Run Anywhere: Creating Portable NGS Analysis Environments with Docker
Never worry about “it works on my machine” again – create portable, reproducible NGS analysis environments Introduction: The Reproducibility Challenge in NGS Analysis Picture this scenario: you’ve spent weeks perfecting your ChIP-seq analysis pipeline on your local workstation. The results are beautiful, the workflow is smooth, and everything runs flawlessly. Then comes the moment of…
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Categories
- ATAC-seq (2)
- bulk RNA-seq (27)
- chromatin accessibility (14)
- Database (4)
- Epigenetics (14)
- Genomics (11)
- HPC (6)
- Metagenomics (1)
- Quick Tips (1)
- RNA-seq (20)
- Scientific Programming (6)
- Single Cell Sequencing (22)
- Transcriptomics (28)
Recent Posts
- How to Analyze Single-Cell ATAC-seq Data — A Complete Beginner’s Guide Part 2: Thorough Quality Control with Signac
- How to Analyze Single-Cell ATAC-seq Data — A Complete Beginner’s Guide Part 1: From FASTQ to Peaks
- How to Choose the Best Genome Aligner for a Specific NGS Dataset — A Beginner’s Guide to Read Mapping Tools
- How to Set Up a Bulk RNA-seq Pipeline on an HPC Cluster — A Complete Beginner’s Guide to Nextflow and nf-core/rnaseq
Tags
Alternative Splicing Analysis ATAC-seq BAM ChIP-seq chromatin accessibility CNV DESeq2 Differential Expression edgeR FASTQ GATK Mutect2 gene expression heatmap HOMER HPC Isoform limma MACS2 MAF miRNA miRNA-seq MSigDB Normalization peak calling RNA-seq SLURM somatic mutations Transcript VCF whole genome sequencing