59,525 research outputs found
Cartesian Certainty and the Infinity of the Will
This paper interprets Descartes\u27 conception of certainty as most fundamentally a function of the human will, controlling the cognitive encounter with the world
Simone Weil\u27s Spiritual Critique of Modern Science: An Historical-Critical Assessment
This paper evaluates Simone Weil\u27s philosophy and theology of science from the perspective of an historical phenomenology of science
Large time behaviour of solutions of a system of generalized Burgers equation
In this paper we study the asymptotic behaviour of solutions of a system of
partial differential equations. When the equation reduces to the
Burgers equation and was studied by Hopf. We consider both the inviscid and
viscous case and show a new feature in the asymptotic behaviour.Comment: 9 page
Joint analysis of functional genomic data and genome-wide association studies of 18 human traits
Annotations of gene structures and regulatory elements can inform genome-wide
association studies (GWAS). However, choosing the relevant annotations for
interpreting an association study of a given trait remains challenging. We
describe a statistical model that uses association statistics computed across
the genome to identify classes of genomic element that are enriched or depleted
for loci that influence a trait. The model naturally incorporates multiple
types of annotations. We applied the model to GWAS of 18 human traits,
including red blood cell traits, platelet traits, glucose levels, lipid levels,
height, BMI, and Crohn's disease. For each trait, we evaluated the relevance of
450 different genomic annotations, including protein-coding genes, enhancers,
and DNase-I hypersensitive sites in over a hundred tissues and cell lines. We
show that the fraction of phenotype-associated SNPs that influence protein
sequence ranges from around 2% (for platelet volume) up to around 20% (for LDL
cholesterol); that repressed chromatin is significantly depleted for SNPs
associated with several traits; and that cell type-specific DNase-I
hypersensitive sites are enriched for SNPs associated with several traits (for
example, the spleen in platelet volume). Finally, by re-weighting each GWAS
using information from functional genomics, we increase the number of loci with
high-confidence associations by around 5%.Comment: Fixed typos, included minor clarification
Computational Geometry Column 34
Problems presented at the open-problem session of the 14th Annual ACM
Symposium on Computational Geometry are listed
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