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npInv: accurate detection and genotyping of inversions using long read sub-alignment
BACKGROUND: Detection of genomic inversions remains challenging. Many existing methods primarily target inzversions with a non repetitive breakpoint, leaving inverted repeat (IR) mediated non-allelic homologous recombination (NAHR) inversions largely unexplored. RESULT: We present npInv, a novel too...
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| Publicado no: | BMC Bioinformatics |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6044046/ https://ncbi.nlm.nih.gov/pubmed/30001702 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2252-9 |
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