Background: At any particular location, frequencies of alleles that are associated with adaptive traits are expected to change in future climates through local adaption and migration, including assisted migration (human-implemented when climate change is more rapid than natural migration rates). Making the assumption that the baseline frequencies of alleles across environmental gradients can act as a predictor of patterns in changed climates (typically future but possibly paleo-climates), a methodology is provided by of predicting changes in allele frequencies at the population level.
Methods: The prediction procedure involves a first calibration and prediction step through redundancy analysis (RDA), and a second calibration and prediction step through a generalized additive model (GAM) with a binomial family. As such, the procedure is fundamentally different to an alternative approach recently proposed to predict changes in allele frequencies from canonical correspondence analysis (CCA). The RDA step is based on the Euclidean distance that is also the typical distance used in Analysis of Molecular Variance (AMOVA). Because the RDA step or CCA approach sometimes predict negative allele frequencies, the GAM step ensures that allele frequencies are in the range of 0 to 1.
Results: provides data sets with predicted frequencies and several visualization methods to depict the predicted shifts in allele frequencies from baseline to changed climates. These visualizations include 'dot plot' graphics (function ), pie diagrams (), moon diagrams (), 'waffle' diagrams () and smoothed surface diagrams of allele frequencies of baseline or future patterns in geographical space (). As these visualizations were generated through the package, methods of generating animations for a climate change time series are straightforward, as shown in the documentation of and in the supplemental videos.
Availability: is available as an open-source R package from https://cran.r-project.org/package=AlleleShift and https://github.com/RoelandKindt/AlleleShift. Genetic input data is expected to be in the format, which can be generated from the format. Climate data is available from various resources such as and .
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http://dx.doi.org/10.7717/peerj.11534 | DOI Listing |
Pharmacogenet Genomics
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Reproductive Medicine, Instituto Bernabeu of Fertility and Gynaecology.
The research question is as follows: Are estrogen and progesterone receptor genotypes associated with thin endometrium? We performed a prospective cohort study of 129 patients who underwent preimplantation genetic testing for aneuploidies. These patients were categorized according to endometrial thickness: >7 mm control group (n = 94) and ≤7 mm study group (n = 35). Polymorphisms in the genes ESR1 (rs9340799 and rs3138774), ESR2 (rs1256049 and rs4986938), and PGR (rs1042838) were analyzed.
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1st Department of Neurology, Eginition Hospital, National and Kapodistrian University of Athens, Athens, Greece.
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View Article and Find Full Text PDFIran J Basic Med Sci
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Department of Medical Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
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Front Immunol
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Department of Rheumatology, Oslo University Hospital, Oslo, Norway.
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Eur J Haematol
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Hematology, St. Paul's Hospital and The University of British Columbia, Vancouver, British Columbia, Canada.
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