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Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs
BACKGROUND: The study of genomic variation has provided key insights into the functional role of mutations. Predominantly, studies have focused on single nucleotide variants (SNV), which are relatively easy to detect and can be described with rich mathematical models. However, it has been observed t...
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| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5043639/ https://ncbi.nlm.nih.gov/pubmed/27687569 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-1258-4 |
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