- Point of using Hisat2 build to index reference genomes when working with known genomes mouse/human?
- I used featureCounts to quantify RNA-seq reads and got a low successful alignment percentage. Is this a problem?
- mRNA-seq Read Length Selection
- Recommendations for software or online resources
- How to know where to align if I have RNAseq data??
- Semi Budget-Friendly High-Thread Count Options?
- Best somatic variant callers?
- How to get NGS programming experience?
- Illumina: can I use it on my laptop?
- Nextflow issue
- What is the preferred way of documenting a Nextflow pipeline?
- Software repository and hackathons
- GATK4 automated pipelines in existence?
- Introduction to RNAseq and microRNA?
- Ask HN: How to be my own genetic disease researcher for my partner?
- Generate consensus FASTA files pipeline
- Workflow Question
- Why does it feels impossible to set up github nextflow pipeline without a root?
- Nextflow RNA-seq pipeline
- aws batch keeps the "Desired vCPUs" high long after they should be reduced
- Snakemake vs. nf vs. CWL
- Nextflow question config