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Bauer, M. J.

Publications and source records attributed to Bauer, M. J..

4 recordsLinked to original sources

Causal inference for multiple risk factors and diseases from genomics data

Statistical causal learning in genome-wide association studies (GWAS) relies on the instrumental variable method of Mendelian Randomization (MR). Currently, an over-whelming number of MR studies purport to show causal relationships among a wide range of risk factors and outcomes. Here, we find that naive application of many recently proposed MR approaches results in numerous null relationships being discovered as highly significant. We show that a well-controlled error rate can be achieved through a graphical inference approach which: (i) selects a set of genetic instrumental variables (IVs) from GWAS summary static controlling for LD, linkage and pleiotropy; (ii) accommodates rare variants and binary outcomes in a principled way; (iii) distinguishes direct from indirect risk factors in very high-dimensional data; and (iv) identifies potential unobserved latent confounding. Only 20 minutes of wall-clock compute time is required for our Causal Inference GWAS (CI-GWAS) approach to jointly analyze a set of 9 common health risk factors, four common complex metabolic disease outcomes and 8.4M genetic variants recorded for 458,747 individuals in the UK Biobank. Genome-wide, we find that very few genetic variants are suitable MR IVs, with only 696 variants remaining when analyzing all traits jointly. While we replicate almost all paths previously found by CAUSE between risk factors and outcomes, we show that only few of these reflect direct adjacencies and that many cannot be distinguished from unmeasured confounding within the UK Biobank data. Our results suggest that well-curated longitudinal records and family data are likely needed to overcome the mixtures of temporal precedence and reverse-causality in biobank data. Our approach provides a first-step toward robust principled screening for potential causal links to understand the underlying nature of phenotypic correlations in biobank data.

genetics↗

Kokiri: Random Forest-Based Cohort Comparison and Characterization

AO_SCPLOWBSTRACTC_SCPLOWWe propose an interactive visual analytics approach to characterizing and comparing patient subgroups (i.e., cohorts). Despite having the same disease and similar demographic characteristics, patients respond differently to therapy. One reason for this is the vast number of variables in the genome that influence a patients outcome. Nevertheless, most existing tools do not offer effective means of identifying the attributes that differ most, or look at them in isolation and thus ignore combinatorial effects. To fill this gap, we present Kokiri, a visual analytics approach that aims to separate cohorts based on user-selected data, ranks attributes by their importance in distinguishing between cohorts, and visualizes cohort overlaps and separability. With our approach, users can additionally characterize the homogeneity and outliers of a cohort. To demonstrate the applicability of our approach, we integrated Kokiri into the Coral cohort analysis tool to compare and characterize lung cancer patient cohorts.

bioinformatics↗

Coral: a web-based visual analysis tool for creating and characterizing cohorts

SummaryA main task in computational cancer analysis is the identification of patient subgroups (i.e., cohorts) based on metadata attributes (patient stratification) or genomic markers of response (biomarkers). Coral is a web-based cohort analysis tool that is designed to support this task: Users can interactively create and refine cohorts, which can then be compared, characterized, and inspected down to the level of single items. Coral visualizes the evolution of cohorts and also provides intuitive access to prevalence information. Furthermore, findings can be stored, shared, and reproduced via the integrated session management. Coral is pre-loaded with data from over 128,000 samples from the AACR Project GENIE, The Cancer Genome Atlas, and the Cell Line Encyclopedia. Availability and ImplementationCoral is publicly available at https://coral.caleydoapp.org. The source code is released at https://github.com/Caleydo/coral. Contactthomas.zichner@boehringer-ingelheim.com Supplementary informationSupplementary data are available at Bioinformatics online.

bioinformatics↗

Topically delivered 22 nt siRNAs enhance RNAi silencing of endogenous genes in two species

22 nt miRNAs or siRNAs have been shown to specifically induce production of transitive (secondary) siRNAs for targeted mRNAs. An abrasion method to deliver dsRNAs into leaf cells of intact plants was used to investigate the activities of 21 and 22 nt siRNAs in silencing genes in Nicotiana benthamiana and Amaranthus cruentus. We confirmed that both 21 and 22 nt siRNAs were able to silence a green fluorescent protein (GFP) transgene in treated leaves of N. benthamiana, but systemic silencing of GFP occurred only when the guide strand contained 22 nt. Silencing in the treated leaves of N. benthamiana was demonstrated for 3 endogenous genes: magnesium cheletase subunit I (CHL-I), magnesium cheletase subunit H (CHL-H), and GUN4. However, systemic silencing of these endogenous genes was not observed. Very high levels of transitive siRNAs were produced for GFP in response to treatment with 22 nt siRNAs, but only low levels were produced in response to a 21 nt siRNA. The endogenous genes tested also had more transitive siRNAs produced in response to 22 nt siRNAs, but the response varied from weak (CHL-I) to strong (CHL-H). 22 nt siRNAs produced greater local silencing phenotypes than 21 nt siRNAs for GFP, CHL-H and GUN4 in N. benthamiana. The special activity of 22 nt siRNAs in producing a greater local phenotype and induction of elevated levels of transitive siRNAs was also shown in A. cruentus for the CHL-H gene. These experiments suggest a functional role for transitive siRNAs in amplifying the RNAi response.

plant biology↗