FVC as an adaptive and accurate method for filtering variants from popular NGS analysis pipelines
FVC is a method for calling specific gene variants from whole genome data, for potential use in clinical diagnosis and human genetics research.
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2022-09-01
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| Series: | Communications Biology |
| Online Access: | https://doi.org/10.1038/s42003-022-03397-7 |