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🐬 Fan Zhang, et al, 2017. BMC Bioinformatics. A variational Bayesian model to identify rare variants in heterogeneous NGS clinical samples.

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rvd2-variational

Introduction

We developed a variational EM algorithm for a hierarchical Bayesian model to identify rare variants in heterogeneous next-generation sequencing data. Our algorithm is able to identify variants in a broad range of read depths and non-reference allele frequencies with high sensitivity and specificity. In an analysis of a directed evolution longitudinal yeast data set, we are able to identify a time-series trend in non-reference allele frequency and detect novel variants that have not yet been reported. Our model also detects the emergence of a beneficial variant earlier than was previously shown, and a pair of concomitant variants.

Citation

  • Zhang, F. and Flaherty, P. Variational inference for rare variant detection in deep, heterogeneous next-generation sequencing data. BMC bioinformatics, 18(1), 45, 2017
  • He, Y., Zhang, F., and Flaherty, P. RVD2: an ultra-sensitive variant detection model for low-depth heterogeneous next-generation sequencing data. Bioinformatics, 31(17), 2785-2793, 2015

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🐬 Fan Zhang, et al, 2017. BMC Bioinformatics. A variational Bayesian model to identify rare variants in heterogeneous NGS clinical samples.

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