Comparing the performance of selected variant callers using synthetic data and genome segmentation
Abstract Background High-throughput sequencing has rapidly become an essential part of precision cancer medicine. But validating results obtained from analyzing and interpreting genomic data remains a rate-limiting factor. The gold standard, of course, remains manual validation by expert panels, whi...
| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2018-11-01
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| Series: | BMC Bioinformatics |
| Online Access: | http://link.springer.com/article/10.1186/s12859-018-2440-7 |