scispace - formally typeset
Search or ask a question
Institution

École Polytechnique Fédérale de Lausanne

FacilityLausanne, Switzerland
About: École Polytechnique Fédérale de Lausanne is a facility organization based out in Lausanne, Switzerland. It is known for research contribution in the topics: Population & Catalysis. The organization has 44041 authors who have published 98296 publications receiving 4372092 citations. The organization is also known as: EPFL & ETHL.


Papers
More filters
Journal ArticleDOI
TL;DR: This work shows that systematic adjustment of pump conditions for low phase noise enables coherent data transmission with advanced modulation formats that pose stringent requirements on the spectral purity of the comb and offers an attractive solution towards chip-scale terabit/s transceivers.
Abstract: Optical frequency combs have the potential to revolutionize terabit communications1. Generation of Kerr combs in nonlinear microresonators2 represents a particularly promising option3 enabling line spacings of tens of GHz. However, such combs may exhibit strong phase noise4-6, which has made high-speed data transmission impossible up to now. Here we demonstrate that systematic adjustment of pump conditions for low phase noise4,7-9 enables coherent data transmission with advanced modulation formats that pose stringent requirements on the spectral purity of the comb. In a first experiment, we encode a data stream of 392 Gbit/s on a Kerr comb using quadrature phase shift keying (QPSK) and 16-state quadrature amplitude modulation (16QAM). A second experiment demonstrates feedback-stabilization of the comb and transmission of a 1.44 Tbit/s data stream over up to 300 km. The results show that Kerr combs meet the highly demanding requirements of coherent communications and thus offer an attractive solution towards chip-scale terabit/s transceivers.

606 citations

Journal ArticleDOI
TL;DR: This document reviews phenomenological models of short-term and long-term synaptic plasticity, in particular spike-timing dependent plasticity (STDP), and focuses on phenomenological synaptic models that are compatible with integrate-and-fire type neuron models where each neuron is described by a small number of variables.
Abstract: Synaptic plasticity is considered to be the biological substrate of learning and memory. In this document we review phenomenological models of short-term and long-term synaptic plasticity, in particular spike-timing dependent plasticity (STDP). The aim of the document is to provide a framework for classifying and evaluating different models of plasticity. We focus on phenomenological synaptic models that are compatible with integrate-and-fire type neuron models where each neuron is described by a small number of variables. This implies that synaptic update rules for short-term or long-term plasticity can only depend on spike timing and, potentially, on membrane potential, as well as on the value of the synaptic weight, or on low-pass filtered (temporally averaged) versions of the above variables. We examine the ability of the models to account for experimental data and to fulfill expectations derived from theoretical considerations. We further discuss their relations to teacher-based rules (supervised learning) and reward-based rules (reinforcement learning). All models discussed in this paper are suitable for large-scale network simulations.

606 citations

Journal ArticleDOI
03 Apr 2008-Nature
TL;DR: A population of cells in early epidermal tumours characterized by phenotypic and functional similarities to normal bulge skin stem cells is identified and β-catenin signalling is described as being essential in sustaining the CSC phenotype.
Abstract: Continuous turnover of epithelia is ensured by the extensive self-renewal capacity of tissue-specific stem cells. Similarly, epithelial tumour maintenance relies on cancer stem cells (CSCs), which co-opt stem cell properties. For most tumours, the cellular origin of these CSCs and regulatory pathways essential for sustaining stemness have not been identified. In murine skin, follicular morphogenesis is driven by bulge stem cells that specifically express CD34. Here we identify a population of cells in early epidermal tumours characterized by phenotypic and functional similarities to normal bulge skin stem cells. This population contains CSCs, which are the only cells with tumour initiation properties. Transplants derived from these CSCs preserve the hierarchical organization of the primary tumour. We describe beta-catenin signalling as being essential in sustaining the CSC phenotype. Ablation of the beta-catenin gene results in the loss of CSCs and complete tumour regression. In addition, we provide evidence for the involvement of increased beta-catenin signalling in malignant human squamous cell carcinomas. Because Wnt/beta-catenin signalling is not essential for normal epidermal homeostasis, such a mechanistic difference may thus be targeted to eliminate CSCs and consequently eradicate squamous cell carcinomas.

606 citations

Journal ArticleDOI
TL;DR: This tutorial overview outlines the main challenges of the emerging field of signal processing on graphs, discusses different ways to define graph spectral domains, which are the analogs to the classical frequency domain, and highlights the importance of incorporating the irregular structures of graph data domains when processing signals on graphs.
Abstract: In applications such as social, energy, transportation, sensor, and neuronal networks, high-dimensional data naturally reside on the vertices of weighted graphs. The emerging field of signal processing on graphs merges algebraic and spectral graph theoretic concepts with computational harmonic analysis to process such signals on graphs. In this tutorial overview, we outline the main challenges of the area, discuss different ways to define graph spectral domains, which are the analogues to the classical frequency domain, and highlight the importance of incorporating the irregular structures of graph data domains when processing signals on graphs. We then review methods to generalize fundamental operations such as filtering, translation, modulation, dilation, and downsampling to the graph setting, and survey the localized, multiscale transforms that have been proposed to efficiently extract information from high-dimensional data on graphs. We conclude with a brief discussion of open issues and possible extensions.

606 citations

Journal ArticleDOI
TL;DR: This work describes how it has produced a consensus metabolic network reconstruction for S. cerevisiae, and places special emphasis on referencing molecules to persistent databases or using database-independent forms, such as SMILES or InChI strings, as this permits their chemical structure to be represented unambiguously and in a manner that permits automated reasoning.
Abstract: Genomic data allow the large-scale manual or semi-automated assembly of metabolic network reconstructions, which provide highly curated organism-specific knowledge bases. Although several genome-scale network reconstructions describe Saccharomyces cerevisiae metabolism, they differ in scope and content, and use different terminologies to describe the same chemical entities. This makes comparisons between them difficult and underscores the desirability of a consolidated metabolic network that collects and formalizes the 'community knowledge' of yeast metabolism. We describe how we have produced a consensus metabolic network reconstruction for S. cerevisiae. In drafting it, we placed special emphasis on referencing molecules to persistent databases or using database-independent forms, such as SMILES or InChI strings, as this permits their chemical structure to be represented unambiguously and in a manner that permits automated reasoning. The reconstruction is readily available via a publicly accessible database and in the Systems Biology Markup Language (http://www.comp-sys-bio.org/yeastnet). It can be maintained as a resource that serves as a common denominator for studying the systems biology of yeast. Similar strategies should benefit communities studying genome-scale metabolic networks of other organisms.

605 citations


Authors

Showing all 44420 results

NameH-indexPapersCitations
Michael Grätzel2481423303599
Ruedi Aebersold182879141881
Eliezer Masliah170982127818
Richard H. Friend1691182140032
G. A. Cowan1592353172594
Ian A. Wilson15897198221
Johan Auwerx15865395779
Menachem Elimelech15754795285
A. Artamonov1501858119791
Melody A. Swartz1481304103753
Henry J. Snaith146511123155
Kurt Wüthrich143739103253
Richard S. J. Frackowiak142309100726
Jean-Paul Kneib13880589287
Kevin J. Tracey13856182791
Network Information
Related Institutions (5)
ETH Zurich
122.4K papers, 5.1M citations

98% related

Massachusetts Institute of Technology
268K papers, 18.2M citations

96% related

Georgia Institute of Technology
119K papers, 4.6M citations

96% related

Centre national de la recherche scientifique
382.4K papers, 13.6M citations

96% related

University of Illinois at Urbana–Champaign
225.1K papers, 10.1M citations

94% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023234
2022704
20215,247
20205,644
20195,432
20185,094