nch-igm/VarRNA: Initial release - v1.0.0
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| Autores principales: | , |
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| Formato: | Recurso digital |
| Publicado: |
Zenodo
2025
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| _version_ | 1866902065248206848 |
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| author | audrey-bollas Grant Lammi |
| author_facet | audrey-bollas Grant Lammi |
| contents | <p>This is the first release of VarRNA, which accompanies the manuscript submission titled "Variant calling from RNA-Seq data reveals allele-specific differential expression of pathogenic cancer variants". Features include:</p> <ul> <li>RNA-Seq data processing (STAR alignment, GATK variant calling);</li> <li>Feature annotation with ANNOVAR; and</li> <li>Our model to classify variants as germline, somatic, or artifact.</li> </ul> |
| format | Recurso digital |
| id | zenodo_https___doi_org_10_5281_zenodo_14699945 |
| institution | Zenodo |
| language | |
| publishDate | 2025 |
| publisher | Zenodo |
| record_format | zenodo |
| spellingShingle | nch-igm/VarRNA: Initial release - v1.0.0 audrey-bollas Grant Lammi <p>This is the first release of VarRNA, which accompanies the manuscript submission titled "Variant calling from RNA-Seq data reveals allele-specific differential expression of pathogenic cancer variants". Features include:</p> <ul> <li>RNA-Seq data processing (STAR alignment, GATK variant calling);</li> <li>Feature annotation with ANNOVAR; and</li> <li>Our model to classify variants as germline, somatic, or artifact.</li> </ul> |
| title | nch-igm/VarRNA: Initial release - v1.0.0 |
| url | https://doi.org/10.5281/zenodo.14699945 |