اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدCausal Discovery in the Presence of Measurement Error: Identifiability Conditions
80
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Measurement error in the observed values of the variables can greatly change the output of various causal discovery methods. This problem has received much attention in multiple fields, but it is not clear to what extent the causal model for the measurement-error-free variables can be identified in the presence of measurement error with unknown variance. In this paper, we study precise sufficient identifiability conditions for the measurement-error-free causal model and show what information of the causal model can be recovered from observed data. In particular, we present two different sets of identifiability conditions, based on the second-order statistics and higher-order statistics of the data, respectively. The former was inspired by the relationship between the generating model of the measurement-error-contaminated data and the factor analysis model, and the latter makes use of the identifiability result of the over-complete independent component analysis problem.
قيم البحث
اقرأ أيضاً
Many real-world decision-making tasks require learning casual relationships between a set of variables. Typical causal discovery methods, however, require that all variables are observed, which might not be realistic in practice. Unfortunately, in th
e presence of latent confounding, recovering casual relationships from observational data without making additional assumptions is an ill-posed problem. Fortunately, in practice, additional structure among the confounders can be expected, one such example being pervasive confounding, which has been exploited for consistent causal estimation in the special case of linear causal models. In this paper, we provide a proof and method to estimate causal relationships in the non-linear, pervasive confounding setting. The heart of our procedure relies on the ability to estimate the pervasive confounding variation through a simple spectral decomposition of the observed data matrix. We derive a DAG score function based on this insight, and empirically compare our method to existing procedures. We show improved performance on both simulated and real datasets by explicitly accounting for both confounders and non-linear effects.
Our goal is to estimate causal interactions in multivariate time series. Using vector autoregressive (VAR) models, these can be defined based on non-vanishing coefficients belonging to respective time-lagged instances. As in most cases a parsimonious
causality structure is assumed, a promising approach to causal discovery consists in fitting VAR models with an additional sparsity-promoting regularization. Along this line we here propose that sparsity should be enforced for the subgroups of coefficients that belong to each pair of time series, as the absence of a causal relation requires the coefficients for all time-lags to become jointly zero. Such behavior can be achieved by means of l1-l2-norm regularized regression, for which an efficient active set solver has been proposed recently. Our method is shown to outperform standard methods in recovering simulated causality graphs. The results are on par with a second novel approach which uses multiple statistical testing.
Unobserved confounding presents a major threat to causal inference from observational studies. Recently, several authors suggest that this problem may be overcome in a shared confounding setting where multiple treatments are independent given a commo
n latent confounder. It has been shown that under a linear Gaussian model for the treatments, the causal effect is not identifiable without parametric assumptions on the outcome model. In this paper, we show that the causal effect is indeed identifiable if we assume a general binary choice model for the outcome with a non-probit link. Our identification approach is based on the incongruence between Gaussianity of the treatments and latent confounder, and non-Gaussianity of a latent outcome variable. We further develop a two-step likelihood-based estimation procedure.
Causal discovery from observational data is a challenging task to which an exact solution cannot always be identified. Under assumptions about the data-generative process, the causal graph can often be identified up to an equivalence class. Proposing
new realistic assumptions to circumscribe such equivalence classes is an active field of research. In this work, we propose a new set of assumptions that constrain possible causal relationships based on the nature of the variables. We thus introduce typed directed acyclic graphs, in which variable types are used to determine the validity of causal relationships. We demonstrate, both theoretically and empirically, that the proposed assumptions can result in significant gains in the identification of the causal graph.
In time-to-event settings, the presence of competing events complicates the definition of causal effects. Here we propose the new separable effects to study the causal effect of a treatment on an event of interest. The separable direct effect is the
treatment effect on the event of interest not mediated by its effect on the competing event. The separable indirect effect is the treatment effect on the event of interest only through its effect on the competing event. Similar to Robins and Richardsons extended graphical approach for mediation analysis, the separable effects can only be identified under the assumption that the treatment can be decomposed into two distinct components that exert their effects through distinct causal pathways. Unlike existing definitions of causal effects in the presence of competing events, our estimands do not require cross-world contrasts or hypothetical interventions to prevent death. As an illustration, we apply our approach to a randomized clinical trial on estrogen therapy in individuals with prostate cancer.
الأسئلة المقترحة
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
