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Predicting target genes of non-coding regulatory variants with IRT
SUMMARY: Interpreting genetic variants of unknown significance (VUS) is essential in clinical applications of genome sequencing for diagnosis and personalized care. Non-coding variants remain particularly difficult to interpret, despite making up a large majority of trait associations identified in...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7575052/ https://ncbi.nlm.nih.gov/pubmed/32330225 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btaa254 |
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