bioRxiv Science⌕ Search

Biology subjects

Zöllner, S.

Publications and source records attributed to Zöllner, S..

3 recordsLinked to original sources

LoGicAl: Local Ancestry and Genotype Calling Uncertainty-aware Ancestry-specific Allele Frequency Estimation from Admixed Samples

In admixed groups, it is of interest to estimate allele frequencies of their ancestral contributing populations. These ancestry-specific allele frequencies inform genetic drivers of disease etiologies, facilitate genome-wide association study interpretations, enhance polygenic risk prediction and portability, and provide insights into demographic history. Their estimation leverages inferred locus-specific ancestry background, i.e., local ancestry, generated by tools like RFMix. However, existing estimation methods lose accuracy and incur biases by failing to model uncertainty from upstream local ancestry inference and genotype calling. Here, we introduce LoGicAl, a novel likelihood-based method for estimating ancestry-specific allele frequencies from admixed samples, simultaneously accommodating uncertainty from ancestry calling, genotyping, and statistical phasing. We demonstrate that modeling these uncertainties substantially reduces estimation errors, resulting in superior accuracy for both sequence-based and array-based genotyping with different levels of local ancestry inference quality. By integrating an accelerated fixed-point algorithm, LoGicAl achieves high scalability and enhanced computational efficiency compared with existing approaches. Applying LoGicAl to admixed cohorts in the 1000 Genomes Project, we illustrate the benefits of local-ancestry-based allele frequency estimates. Together, LoGicAl contributes to genomic analyses of admixed samples by providing precise and rapid ancestry-specific allele frequency estimates, and to constructing the spatial landscape and dynamics of genetic variations in admixed populations at a finer scale.

genetics↗

Gene-Set Enrichment with Mathematical Biology (GEMB)

Gene-set analyses measure the association between a disease of interest and a set of genes related to a biological pathway. These analyses often incorporate gene network properties to account for the differential contributions of each gene. Extending this concept further, mathematical models of biology can be leveraged to define gene interactions based on biophysical principles by predicting the effects of genetic perturbations on a particular downstream function. We present a method that combines gene weights from model predictions and gene ranks from genome-wide association studies into a weighted gene-set test. Using publicly-available summary data from the Psychiatric Genetics Consortium (n=41,653; ~9) million SNPs), we examine an a priori hypothesis that intracellular calcium ion concentrations contribute to bipolar disorder. In this case study, we are able to strengthen inferences from a P-value of 0.081 to 1.7x10-4 by moving from a general calcium signaling pathway to a specific model-predicted function.

genetics↗

Helmsman: fast and efficient generation of input matrices for mutation signature analysis

MotivationThe spectrum of somatic single-nucleotide variants in cancer genomes often reflects the signatures of multiple distinct mutational processes, which can provide clinically actionable insights into cancer etiology. Existing software tools for identifying and evaluating these mutational signatures do not scale to analyze large datasets containing thousands of individuals or millions of variants.\n\nResultsWe introduce Helmsman, a program designed to rapidly generate mutation spectra matrices from arbitrarily large datasets. Helmsman is up to 300 times faster than existing methods and can provide more than a 100-fold reduction in memory usage, making mutation signature analysis tractable for any collection of single nucleotide variants, no matter how large.\n\nAvailabilityHelmsman is freely available for download at https://github.com/carjed/helmsman under the MIT license. Detailed documentation can be found at https://www.jedidiahcarlson.com/docs/helmsman/, and an interactive Jupyter notebook containing a guided tutorial can be accessed at https://mybinder.org/v2/gh/carjed/helmsman/master.\n\nContactjedidiah@umich.edu\n\nSupplementary informationSupplementary information for this article is available.

bioinformatics↗