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Origins and characterization of variants shared between databases of somatic and germline human mutations
BACKGROUND: Mutations arise in the human genome in two major settings: the germline and the soma. These settings involve different inheritance patterns, time scales, chromatin structures, and environmental exposures, all of which impact the resulting distribution of substitutions. Nonetheless, many...
Uloženo v:
| Vydáno v: | BMC Bioinformatics |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7273669/ https://ncbi.nlm.nih.gov/pubmed/32498674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-3508-8 |
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