24 research outputs found
Age at first birth in women is genetically associated with increased risk of schizophrenia
Prof. Paunio on PGC:n jäsenPrevious studies have shown an increased risk for mental health problems in children born to both younger and older parents compared to children of average-aged parents. We previously used a novel design to reveal a latent mechanism of genetic association between schizophrenia and age at first birth in women (AFB). Here, we use independent data from the UK Biobank (N = 38,892) to replicate the finding of an association between predicted genetic risk of schizophrenia and AFB in women, and to estimate the genetic correlation between schizophrenia and AFB in women stratified into younger and older groups. We find evidence for an association between predicted genetic risk of schizophrenia and AFB in women (P-value = 1.12E-05), and we show genetic heterogeneity between younger and older AFB groups (P-value = 3.45E-03). The genetic correlation between schizophrenia and AFB in the younger AFB group is -0.16 (SE = 0.04) while that between schizophrenia and AFB in the older AFB group is 0.14 (SE = 0.08). Our results suggest that early, and perhaps also late, age at first birth in women is associated with increased genetic risk for schizophrenia in the UK Biobank sample. These findings contribute new insights into factors contributing to the complex bio-social risk architecture underpinning the association between parental age and offspring mental health.Peer reviewe
Discovery of widespread transcription initiation at microsatellites predictable by sequence-based deep neural network
Using the Cap Analysis of Gene Expression (CAGE) technology, the FANTOM5 consortium provided one of the most comprehensive maps of transcription start sites (TSSs) in several species. Strikingly, ~72% of them could not be assigned to a specific gene and initiate at unconventional regions, outside promoters or enhancers. Here, we probe these unassigned TSSs and show that, in all species studied, a significant fraction of CAGE peaks initiate at microsatellites, also called short tandem repeats (STRs). To confirm this transcription, we develop Cap Trap RNA-seq, a technology which combines cap trapping and long read MinION sequencing. We train sequence-based deep learning models able to predict CAGE signal at STRs with high accuracy. These models unveil the importance of STR surrounding sequences not only to distinguish STR classes, but also to predict the level of transcription initiation. Importantly, genetic variants linked to human diseases are preferentially found at STRs with high transcription initiation level, supporting the biological and clinical relevance of transcription initiation at STRs. Together, our results extend the repertoire of non-coding transcription associated with DNA tandem repeats and complexify STR polymorphism
Right Honorable Herb Gray, P.S., C.C., Q.C., The Session 8: Canada and U.S. Approaches to the Great Lakes
environmental law--Canada, environmental law--United States, Great Lake
Molecular Epidemiology of H5N1 Avian Influenza Virus: Correlations between Antigenic Drift, Geographical Migration and Expansion of Viral Diversity
Performance Analysis of Least Load Multicast Routing for Single Rate Loss Networks
In this paper, we investigate a state dependent multicast routing algorithm called Least Load Multicast Routing (LLMR), for single rate loss networks. The algorithm is based on Least Load Routing (LLR) concept and the approach is to select the least load links for establishing connections. The networks considered are assumed fully connected. In addition, connection requests are Poisson arrival and the holding times of accepted calls are exponentially distributed. The analytical model that we developed for calculating blocking probabilities is based on the link independence assumption and the Reduced Load Approximation (RLA). Analytical results are compared with simulation results and the agreement is surprisingly good. We find that the effect of link independence assumption is insignificant for the analytical model
Exome sequencing in paediatric patients with movement disorders
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230163.pdf (publisher's version ) (Open Access