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Read count-based method for high-throughput allelic genotyping of transposable elements and structural variants
BACKGROUND: Like other structural variants, transposable element insertions can be highly polymorphic across individuals. Their functional impact, however, remains poorly understood. Current genome-wide approaches for genotyping insertion-site polymorphisms based on targeted or whole-genome sequenci...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMC Genomics |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4494700/ https://ncbi.nlm.nih.gov/pubmed/26153459 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-1700-4 |
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