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Mentions
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Stars | Project | Description | |
|---|---|---|---|---|
| We couldn't find any libraries for the selected period | ||||
Popular Nextflow Topics
Latest Mentions
Latest mentioned Nextflow repos
| Stars | Project |
|---|---|
| 770 | rnaseq |
| 0 | MSAR-core_bulkRNAseq |
| 333 | sarek |
| 160 | atacseq |
| 169 | chipseq |
| 3 | dragen-variant-calling |
| 182 | mag |
| 11 | GATK |
| 56 | rare-disease-wf |
| 52 | hlatyping |
| 125 | eager |
| 77 | configs |
| 28 | rnatoy |
| 62 | rnaseq-nf |
| 316 | patterns |
Latest Discoveries
Latest discovered Nextflow repos
| Stars | Project |
|---|---|
| 0 | MSAR-core_bulkRNAseq |
| 169 | chipseq |
| 3 | dragen-variant-calling |
| 160 | atacseq |
| 11 | GATK |
| 56 | rare-disease-wf |
| 52 | hlatyping |
| 770 | rnaseq |
| 182 | mag |
| 125 | eager |
| 77 | configs |
| 28 | rnatoy |
| 333 | sarek |
| 62 | rnaseq-nf |
| 316 | patterns |
Recently updated posts
- 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??