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AGE: defining breakpoints of genomic structural variants at single-nucleotide resolution, through optimal alignments with gap excision
Motivation: Defining the precise location of structural variations (SVs) at single-nucleotide breakpoint resolution is an important problem, as it is a prerequisite for classifying SVs, evaluating their functional impact and reconstructing personal genome sequences. Given approximate breakpoint loca...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2011
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3042181/ https://ncbi.nlm.nih.gov/pubmed/21233167 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq713 |
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