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Ting Chen

Publications and source records attributed to Ting Chen.

2 recordsLinked to original sources

mLDM: a new hierarchical Bayesian statistical model for sparse microbioal association discovery

Interpretive analysis of metagenomic data depends on an understanding of the underlying associations among microbes from metagenomic samples. Although several statistical tools have been developed for metage-nomic association studies, they suffer from compositional bias or fail to take into account environmental factors that directly affect the composition of a given microbial community. In this paper, we propose metagenomic Lognormal-Dirichlet-Multinomial (mLDM), a hierarchical Bayesian model with sparsity constraints to bypass compositional bias and discover new associations among microbes and between microbes and environmental factors. The mLD-M model can 1) infer both conditionally dependent associations among microbes and direct associations between microbes and environmental factors; 2) consider both compositional bias and variance of metagenomic data; and 3) estimate absolute abundance for microbes. Thus, conditionally dependent association can capture direct relationship underlying microbial pairs and remove the indirect connections induced from other common factors. Empirical studies show the effectiveness of the mLDM model, using both synthetic data and the TARA Oceans eukaryotic data by comparing it with several state-of-the-art methodologies. Finally, mLDM is applied to western English Channel data and finds some interesting associations.

Bioinformatics

ProbAlign: a re-alignment method for long sequencing reads

The incorrect alignments are a severe problem in variant calling, and remain as a challenge computational issue in Bioinformatics field. Although there have been some methods utilizing the re-alignment approach to tackle the misalignments, a standalone re-alignment tool for long sequencing reads is lacking. Hence, we present a standalone tool to correct the misalignments, called ProbAlign. It can be integrated into the pipelines of not only variant calling but also other genomic applications. We demonstrate the use of re-alignment in two diverse and important genomics fields: variant calling and viral quasispecies reconstruction. First, variant calling results in the Pacific Biosciences SMRT re-sequencing data of NA12878 show that false positives can be reduced by 43.5%, and true positives can be increased by 24.8% averagely, after re-alignment. Second, results in reconstructing a 5-virus-mix show that the viral population can be completely unraveled, and also the estimation of quasispecies frequencies has been improved, after re-alignment. ProbAlign is freely available in the PyroTools toolkit (https://github.com/homopolymer/PyroTools).

Bioinformatics