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germline-variant-calling-pipeline
germline-variant-calling-pipeline PublicA workflow for germline variant calling from raw sequencing data. Covers quality control, alignment, variant calling, filtering, and annotation.
Python
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RNASeq-Analysis-Pipeline
RNASeq-Analysis-Pipeline PublicA complete RNA-Seq analysis workflow, from raw FASTQ files to Differential Gene Expression (DGE) analysis. Includes quality control, read alignment, quantification, normalization, statistical testi…
R
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scRNA-seq-Seurat-Workflow
scRNA-seq-Seurat-Workflow PublicA modular and reproducible Snakemake workflow for single-cell RNA-seq analysis using the Seurat R package. This pipeline processes 10x Genomics PBMC3k data from quality control through clustering a…
R 1
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somatic-variant-calling-pipeline
somatic-variant-calling-pipeline PublicA workflow for somatic variant calling in tumor-normal paired samples. Includes quality control, alignment, variant detection, filtering, annotation, and downstream analysis.
Python
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rnaseq-atacseq-integration-workflow
rnaseq-atacseq-integration-workflow PublicThis Snakemake-based workflow provides a modular and reproducible pipeline for processing and integrating bulk RNA-seq and ATAC-seq datasets. It covers raw data preprocessing, quality control, alig…
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GermlineSNPs-NF
GermlineSNPs-NF PublicNextflow pipeline for germline SNP analysis using BWA, GATK, and SnpEff in a Singularity container.
Nextflow
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