activity
20122019
most citedDefining Predictive Probability Functions for Species Sampling Models

49 citations · 181 across the 10 of their papers we have counts for

collaborators

10 papers

stat.AP2019

A Semi-parametric Bayesian Approach to Population Finding with Time-to-Event and Toxicity Data in a Randomized Clinical Trial

Satoshi Morita, Peter Müller, Hiroyasu Abe

A utility-based Bayesian population finding (BaPoFi) method was proposed by Morita and Müller (2017, Biometrics, 1355-1365) to analyze data from a randomized clinical trial with th…

stat.CO2019★ 1 cited

Consensus Monte Carlo for Random Subsets using Shared Anchors

Yang Ni, Yuan Ji, Peter Mueller

We present a consensus Monte Carlo algorithm that scales existing Bayesian nonparametric models for clustering and feature allocation to big data. The algorithm is valid for any pr…

stat.AP2017★ 1 cited

TreeClone: Reconstruction of Tumor Subclone Phylogeny Based on Mutation Pairs using Next Generation Sequencing Data

Tianjian Zhou, Subhajit Sengupta, Peter Mueller +1

We present TreeClone, a latent feature allocation model to reconstruct tumor subclones subject to phylogenetic evolution that mimics tumor evolution. Similar to most current method…

stat.AP2017★ 8 cited

PairClone: A Bayesian Subclone Caller Based on Mutation Pairs

Tianjian Zhou, Peter Mueller, Subhajit Sengupta +1

Tumor cell populations can be thought of as being composed of homogeneous cell subpopulations, with each subpopulation being characterized by overlapping sets of single nucleotide…

stat.ME2016

Heterogeneous Reciprocal Graphical Models

Yang Ni, Peter Mueller, Yitan Zhu +1

We develop novel hierarchical reciprocal graphical models to infer gene networks from heterogeneous data. In the case of data that can be naturally divided into known groups, we pr…

stat.AP2015★ 31 cited

A Bayesian feature allocation model for tumor heterogeneity

Juhee Lee, Peter Müller, Kamalakar Gulukota +1

We develop a feature allocation model for inference on genetic tumor variation using next-generation sequencing data. Specifically, we record single nucleotide variants (SNVs) base…