Molecular sequence data from rapidly evolving organisms are often sampled at different points in time. Sampling times can then be used for molecular clock calibration. The root-to-tip (RTT) regression is an essential tool to assess the degree to which the data behave in a clock-like fashion. Here, we introduce Clockor2, a client-side web application for conducting RTT regression. Clockor2 allows users to quickly fit local and global molecular clocks, thus handling the increasing complexity of genomic datasets that sample beyond the assumption of homogeneous host populations. Clockor2 is efficient, handling trees of up to the order of 104 tips, with significant speed increases compared with other RTT regression applications. Although clockor2 is written as a web application, all data processing happens on the client-side, meaning that data never leave the user's computer. Clockor2 is freely available at https://clockor2.github.io/.
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http://dx.doi.org/10.1093/sysbio/syae003 | DOI Listing |
Sci Rep
December 2024
Departemnt of Pediatrics and Child Health, School of Medicine, University of Gondar, P.O.Box: 196, Gondar, Ethiopia.
Neonatal hypothermia is a significant global problem of neonates with huge contribution of neonatal morbidity and mortality. Recognizing major contributors of neonatal hypothermia is very important in designing preventing methods which was the objective of our study. This was an institution-based cross-sectional study conducted on 339 neonates admitted to Neonatal Intensive Care Unit of University of Gondar Comprehensive Specialized Hospital over 6months.
View Article and Find Full Text PDFFront Endocrinol (Lausanne)
November 2024
Unit of Pediatrics, Department of Human Pathology of Adulthood and Childhood, University of Messina, Messina, Italy.
Background: Rett syndrome (RTT) is an X-linked progressive neurodevelopmental disorder that involves mainly girls and is the second most frequent cause of genetic intellectual disability. RTT leads to neurological regression between 6 and 18 months of life and could be associated with a variable neurological impairment. However, RTT affects not only neurological function but also wide aspects of non-neurological organs.
View Article and Find Full Text PDFNat Rev Dis Primers
November 2024
Department of Neurology, Boston Children's Hospital, Boston, MA, USA.
Rett syndrome (RTT) is a severe, progressive, neurodevelopmental disorder, which affects predominantly females. In most cases, RTT is associated with pathogenic variants in MECP2. MeCP2, the protein product of MECP2, is known to regulate gene expression and is highly expressed in the brain.
View Article and Find Full Text PDFJ Neurodev Disord
October 2024
Centre for Child Health Research, The Kids Research Institute Australia, University of Western Australia, 15 Hospital Avenue, Nedlands, WA, 6009, Australia.
Introduction: Rett syndrome (RTT) is a rare neurodevelopmental disorder with developmental impairments, comorbidities, and abnormal behaviours such as hand stereotypies and emotional features. The Rett Syndrome Behaviour Questionnaire (RSBQ) was developed to describe the behavioural and emotional features of RTT. Little is known how RSBQ scores are associated with genetic and clinical characteristics in RTT.
View Article and Find Full Text PDFCommun Biol
October 2024
Medical Microbiology and Immunology, School of Medicine, University of California, Davis, CA, USA.
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