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Using genotype array data to compare multi- and single-sample variant calls and improve variant call sets from deep coverage whole-genome sequencing data
MOTIVATION: Variant calling from next-generation sequencing (NGS) data is susceptible to false positive calls due to sequencing, mapping and other errors. To better distinguish true from false positive calls, we present a method that uses genotype array data from the sequenced samples, rather than p...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Bioinformatics |
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| Κύριοι συγγραφείς: | , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Oxford University Press
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5408850/ https://ncbi.nlm.nih.gov/pubmed/28035032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btw786 |
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