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An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome
BACKGROUND: Small insertions and deletions (indels) have a significant influence in human disease and, in terms of frequency, they are second only to single nucleotide variants as pathogenic mutations. As the majority of mutations associated with complex traits are located outside the exome, it is c...
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| Veröffentlicht in: | BMC Bioinformatics |
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| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5955213/ https://ncbi.nlm.nih.gov/pubmed/28985712 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1862-y |
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