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