Institution
Carnegie Mellon University
Education•Pittsburgh, Pennsylvania, United States•
About: Carnegie Mellon University is a education organization based out in Pittsburgh, Pennsylvania, United States. It is known for research contribution in the topics: Population & Robot. The organization has 36317 authors who have published 104359 publications receiving 5975734 citations. The organization is also known as: CMU & Carnegie Mellon.
Papers published on a yearly basis
Papers
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09 Jul 1995TL;DR: The results show that a learning algorithm based on the Minimum Description Length (MDL) principle was able to raise the percentage of interesting articles to be shown to users from 14% to 52% on average.
Abstract: A significant problem in many information filtering systems is the dependence on the user for the creation and maintenance of a user profile, which describes the user's interests. NewsWeeder is a netnews-filtering system that addresses this problem by letting the user rate his or her interest level for each article being read (1-5), and then learning a user profile based on these ratings. This paper describes how NewsWeeder accomplishes this task, and examines the alternative learning methods used. The results show that a learning algorithm based on the Minimum Description Length (MDL) principle was able to raise the percentage of interesting articles to be shown to users from 14% to 52% on average. Further, this performance significantly outperformed (by 21%) one of the most successful techniques in Information Retrieval (IR), term-frequency/inverse-document-frequency (tf-idf) weighting.
2,234 citations
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Icahn School of Medicine at Mount Sinai1, Carnegie Mellon University2, Harvard University3, University of Toronto4, Wellcome Trust Sanger Institute5, University of Pittsburgh6, Nagoya University7, University of Freiburg8, King's College London9, Vanderbilt University10, University of Santiago de Compostela11, King Abdulaziz University12, University of Utah13, Duke University14, Memorial University of Newfoundland15, Trinity College, Dublin16, University of Pennsylvania17, University of Illinois at Chicago18, Boston Children's Hospital19, Columbia University20, German Cancer Research Center21, University College London22, Kaiser Permanente23, Broad Institute24, Cardiff University25, Complutense University of Madrid26, Newcastle University27, Baylor College of Medicine28, University of California, San Francisco29, RWTH Aachen University30, National Health Service31, McMaster University32, Saarland University33, Karolinska Institutet34, National Institutes of Health35, University of Helsinki36, Emory University37
TL;DR: Using exome sequencing, it is shown that analysis of rare coding variation in 3,871 autism cases and 9,937 ancestry-matched or parental controls implicates 22 autosomal genes at a false discovery rate of < 0.05, plus a set of 107 genes strongly enriched for those likely to affect risk (FDR < 0.30).
Abstract: The genetic architecture of autism spectrum disorder involves the interplay of common and rare variants and their impact on hundreds of genes. Using exome sequencing, here we show that analysis of rare coding variation in 3,871 autism cases and 9,937 ancestry-matched or parental controls implicates 22 autosomal genes at a false discovery rate (FDR) < 0.05, plus a set of 107 autosomal genes strongly enriched for those likely to affect risk (FDR < 0.30). These 107 genes, which show unusual evolutionary constraint against mutations, incur de novo loss-of-function mutations in over 5% of autistic subjects. Many of the genes implicated encode proteins for synaptic formation, transcriptional regulation and chromatin-remodelling pathways. These include voltage-gated ion channels regulating the propagation of action potentials, pacemaking and excitability-transcription coupling, as well as histone-modifying enzymes and chromatin remodellers-most prominently those that mediate post-translational lysine methylation/demethylation modifications of histones.
2,228 citations
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TL;DR: DIGE is reproducible, sensitive, and can detect an exogenous difference between two Drosophila embryo extracts at nanogram levels and was detected after 15 min of induction and identified using DIGE preparatively.
Abstract: We describe a modification of two-dimensional (2-D) polyacrylamide gel electrophoresis that requires only a single gel to reproducibly detect differences between two protein samples. This was accomplished by fluorescently tagging the two samples with two different dyes, running them on the same 2-D gel, post-run fluorescence imaging of the gel into two images, and superimposing the images. The amine reactive dyes were designed to insure that proteins common to both samples have the same relative mobility regardless of the dye used to tag them. Thus, this technique, called difference gel electrophoresis (DIGE), circumvents the need to compare several 2-D gels. DIGE is reproducible, sensitive, and can detect an exogenous difference between two Drosophila embryo extracts at nanogram levels. Moreover, an inducible protein from E. coli was detected after 15 min of induction and identified using DIGE preparatively.
2,220 citations
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TL;DR: In this paper, a new method for using the data from Monte Carlo simulations that can increase the efficiency by 2 or more orders of magnitude is presented. But the method is not applicable to statistical models and lattice-gauge theories.
Abstract: We present a new method for using the data from Monte Carlo simulations that can increase the efficiency by 2 or more orders of magnitude. A single Monte Carlo simulation is sufficient to obtain complete thermodynamic information over the entire scaling region near a phase transition. The accuracy of the method is demonstrated by comparison with exact results for the d=2 Ising model. New results for d=2 eight-state Potts model are also presented. The method is generally applicable to statistical models and lattice-gauge theories.
2,219 citations
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TL;DR: In this paper, the authors enumerate a set of discounted utility anomalies analogous to the EU anomalies and propose a model that accounts for the anomalies, as well as other intertemporal choice phenomena incompatible with DU.
Abstract: Research on decision making under uncertainly has been strongly influenced by the documentation of numerous expected utility (EU) anomalies—behaviors that violate the expected utility axioms. The relative lack of progress on the closely related topic of intertemporal choice is partly due to the absence of an analogous set of discounted utility (DU) anomalies. We enumerate a set of DU anomalies analogous to the EU anomalies and propose a model that accounts for the anomalies, as well as other intertemporal choice phenomena incompatible with DU. We discuss implications for savings behavior, estimation of discount rates, and choice framing effects.
2,208 citations
Authors
Showing all 36645 results
Name | H-index | Papers | Citations |
---|---|---|---|
Yi Chen | 217 | 4342 | 293080 |
Rakesh K. Jain | 200 | 1467 | 177727 |
Robert C. Nichol | 187 | 851 | 162994 |
Michael I. Jordan | 176 | 1016 | 216204 |
Jasvinder A. Singh | 176 | 2382 | 223370 |
J. N. Butler | 172 | 2525 | 175561 |
P. Chang | 170 | 2154 | 151783 |
Krzysztof Matyjaszewski | 169 | 1431 | 128585 |
Yang Yang | 164 | 2704 | 144071 |
Geoffrey E. Hinton | 157 | 414 | 409047 |
Herbert A. Simon | 157 | 745 | 194597 |
Yongsun Kim | 156 | 2588 | 145619 |
Terrence J. Sejnowski | 155 | 845 | 117382 |
John B. Goodenough | 151 | 1064 | 113741 |
Scott Shenker | 150 | 454 | 118017 |