Biology subjects

Erdmann-Pham, D. D.

Publications and source records attributed to Erdmann-Pham, D. D..

5 recordsLinked to original sources

bioRxiv2025

Robust and Adaptive Non-Parametric Tests for Detecting General Distributional Shifts in Gene Expression

Differential expression analysis is crucial in genomics, yet existing methods primarily focus on detecting mean shifts. Variance shifts in gene expression are well-documented in studies of cellular signaling pathways, and more recently they have characterized aging, thus motivating the need for flexible detection approaches that include tests of expression variance changes. In this work, we present QRscore (Quantile Rank Score), a general method for detecting distributional shifts in gene expression by extending the Mann-Whitney test into a flexible family of rank-based tests. Here, we focus on implementing QRscore to detect shifts in mean and variance in gene expression, using weights designed from negative binomial (NB) and zero-inflated negative binomial (ZINB) models to combine the strengths of parametric and non-parametric approaches. We show through simulations that QRscore not only achieves high statistical power while controlling the false discovery rate (FDR), but also outperforms existing methods in detecting variance shifts and mean shifts. Applying QRscore to bulk RNA-seq data from the Genotype-Tissue Expression (GTEx) project, we identified numerous differentially dispersed genes and differentially expressed genes across 33 tissues. Notably, many genes have significant variance shifts but non-significant mean shifts. QRscore augments the genome bioinformatics toolkit by offering a powerful and flexible approach for differential expression analysis. QRscore is available in R, at https://github.com/songlab-cal/QRscore.

bioinformatics↗

bioRxiv2023

Tracing cancer evolution and heterogeneity using Hi-C

Chromosomal rearrangements can initiate and drive cancer progression, yet it has been challenging to evaluate their impact, especially in genetically heterogeneous solid cancers. To address this problem we developed HiDENSEC, a new computational framework for analyzing chromatin conformation capture in heterogeneous samples, which can infer somatic copy number alterations, characterize large-scale chromosomal rearrangements, and estimate cancer cell fractions. We validated HiDENSEC with in silico and in vitro controls, and then characterized chromosome-scale evolution during melanoma progression in formalin-fixed tumor samples from three patients. The resulting comprehensive annotation of the genomic events includes copy number neutral translocations that disrupt tumor suppressor genes such as NF1, whole chromosome arm exchanges that result in loss of CDKN2A, and whole-arm copy-number neutral loss of homozygosity involving PTEN. These findings show that large-scale chromosomal rearrangements occur throughout cancer evolution and characterizing these events yields insights into drivers of melanoma progression.

genomics↗

bioRxiv2021

Transferability of Geometric Patterns from Protein Self-Interactions to Protein-Ligand Interactions

There is significant interest in developing machine learning methods to model protein-ligand interactions but a scarcity of experimentally resolved protein-ligand structures to learn from. Protein self-contacts are a much larger source of structural data that could be leveraged, but currently it is not well understood how this data source differs from the target domain. Here, we characterize the 3D geometric patterns of protein self-contacts as probability distributions. We then present a flexible statistical framework to assess the transferability of these patterns to protein-ligand contacts. We observe that the level of transferability from protein self-contacts to protein-ligand contacts depends on contact type, with many contact types exhibiting high transferability. We then demonstrate the potential of leveraging information from these geometric patterns to aid in ligand pose-selection problems in protein-ligand docking. We publicly release our extracted data on geometric interaction patterns to enable further exploration of this problem.

biophysics↗

bioRxiv2020

RNA-Sieve: A likelihood-based deconvolution of bulk gene expression data using single-cell references

Direct comparison of bulk gene expression profiles is complicated by distinct cell type mixtures in each sample which obscure whether observed differences are actually due to changes in expression levels themselves or simply due to differing cell type compositions. Single-cell technology has made it possible to measure gene expression in individual cells, achieving higher resolution at the expense of increased noise. If carefully incorporated, such single-cell data can be used to deconvolve bulk samples to yield accurate estimates of the true cell type proportions, thus enabling one to disentangle the effects of differential expression and cell type mixtures. Here, we propose a generative model and a likelihood-based inference method that uses asymptotic statistical theory and a novel optimization procedure to perform deconvolution of bulk RNA-seq data to produce accurate cell type proportion estimates. We demonstrate the effectiveness of our method, called RNA-Sieve, across a diverse array of scenarios involving real data and discuss extensions made uniquely possible by our probabilistic framework, including a demonstration of well-calibrated confidence intervals.

genomics↗

bioRxiv2018

The key parameters that govern translation efficiency

Translation of mRNA into protein is a fundamental yet complex biological process with multiple factors that can potentially affect its efficiency. In particular, different genes can have quite different initiation rates, while site-specific elongation rates can vary substantially along a given transcript. Here, we analyze a stochastic model of translation dynamics to identify the key parameters that govern the overall rate of protein synthesis and the efficiency of ribosome usage. The mathematical model we study is an interacting particle system that generalizes the Totally Asymmetric Simple Exclusion Process (TASEP), where particles correspond to ribosomes. While the TASEP and its variants have been studied for the past several decades through simulations and mean field approximations, a general analytic solution has remained challenging to obtain. By analyzing the so-called hydrodynamic limit, we here obtain exact closed-form expressions for stationary currents and particle densities that agree well with Monte Carlo simulations. In addition, we provide a complete characterization of phase transitions in the system. Surprisingly, phase boundaries depend on only four parameters: the particle size, and the first, last and minimum particle jump rates. Relating these theoretical results to translation, we formulate four design principles that detail how to tune these parameters to optimize translation efficiency in terms of protein production rate and resource usage. We then analyze ribosome profiling data of S. cerevisiae and demonstrate that its translation system is generally efficient, consistent with the design principles we found. We discuss implications of our findings on evolutionary constraints and codon usage bias.

genomics↗