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SV-Bay: structural variant detection in cancer genomes using a Bayesian approach with correction for GC-content and read mappability
Motivation: Whole genome sequencing of paired-end reads can be applied to characterize the landscape of large somatic rearrangements of cancer genomes. Several methods for detecting structural variants with whole genome sequencing data have been developed. So far, none of these methods has combined...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Bioinformatics |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Oxford University Press
2016
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4896370/ https://ncbi.nlm.nih.gov/pubmed/26740523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv751 |
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