7 research outputs found
In-depth analysis of music structure as a self-organized network
Words in a natural language not only transmit information but also evolve
with the development of civilization and human migration. The same is true for
music. To understand the complex structure behind the music, we introduced an
algorithm called the Essential Element Network (EEN) to encode the audio into
text. The network is obtained by calculating the correlations between scales,
time, and volume. Optimizing EEN to generate Zipfs law for the frequency and
rank of the clustering coefficient enables us to generate and regard the
semantic relationships as words. We map these encoded words into the
scale-temporal space, which helps us organize systematically the syntax in the
deep structure of music. Our algorithm provides precise descriptions of the
complex network behind the music, as opposed to the black-box nature of other
deep learning approaches. As a result, the experience and properties
accumulated through these processes can offer not only a new approach to the
applications of Natural Language Processing (NLP) but also an easier and more
objective way to analyze the evolution and development of music.Comment: 5 page
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)
The Global Parkinson’s Genetics Program (GP2) will genotype over 150,000 participants from around the world, and integrate genetic and clinical data for use in large-scale analyses to dramatically expand our understanding of the genetic architecture of PD. This report details the workflow for cohort integration into the complex arm of GP2, and together with our outline of the monogenic hub in a companion paper, provides a generalizable blueprint for establishing large scale collaborative research consortia
Multi-ancestry genome-wide association meta-analysis of Parkinson?s disease
Although over 90 independent risk variants have been identified for Parkinson’s disease using genome-wide association studies, most studies have been performed in just one population at a time. Here we performed a large-scale multi-ancestry meta-analysis of Parkinson’s disease with 49,049 cases, 18,785 proxy cases and 2,458,063 controls including individuals of European, East Asian, Latin American and African ancestry. In a meta-analysis, we identified 78 independent genome-wide significant loci, including 12 potentially novel loci (MTF2, PIK3CA, ADD1, SYBU, IRS2, USP8, PIGL, FASN, MYLK2, USP25, EP300 and PPP6R2) and fine-mapped 6 putative causal variants at 6 known PD loci. By combining our results with publicly available eQTL data, we identified 25 putative risk genes in these novel loci whose expression is associated with PD risk. This work lays the groundwork for future efforts aimed at identifying PD loci in non-European populations
Light triggering goldsomes enable local NO-generation and alleviate pathological vasoconstriction
Performance Characterization of Dye-Sensitized Photovoltaics under Indoor Lighting
Indoor
utilization of emerging photovoltaics is promising; however,
efficiency characterization under room lighting is challenging. We
report the first round-robin interlaboratory study of performance
measurement for dye-sensitized photovoltaics (cells and mini-modules)
and one silicon solar cell under a fluorescent dim light. Among 15
research groups, the relative deviation in power conversion efficiency
(PCE) of the samples reaches an unprecedented 152%. On the basis of
the comprehensive results, the gap between photometry and radiometry
measurements and the response of devices to the dim illumination are
identified as critical obstacles to the correct PCE. Therefore, we
use an illuminometer as a prime standard with a spectroradiometer
to quantify the intensity of indoor lighting and adopt the reverse-biased
current–voltage (<i>I</i>–<i>V</i>) characteristics as an indicator to qualify the <i>I</i>–<i>V</i> sampling time for dye-sensitized photovoltaics.
The recommendations can brighten the prospects of emerging photovoltaics
for indoor applications
Recommended from our members
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
The Global Parkinson’s Genetics Program (GP2) will genotype over 150,000 participants from around the world, and integrate genetic and clinical data for use in large-scale analyses to dramatically expand our understanding of the genetic architecture of PD. This report details the workflow for cohort integration into the complex arm of GP2, and together with our outline of the monogenic hub in a companion paper, provides a generalizable blueprint for establishing large scale collaborative research consortia
Recommended from our members
Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease
Although over 90 independent risk variants have been identified for Parkinson’s disease using genome-wide association studies, most studies have been performed in just one population at a time. Here we performed a large-scale multi-ancestry meta-analysis of Parkinson’s disease with 49,049 cases, 18,785 proxy cases and 2,458,063 controls including individuals of European, East Asian, Latin American and African ancestry. In a meta-analysis, we identified 78 independent genome-wide significant loci, including 12 potentially novel loci (MTF2, PIK3CA, ADD1, SYBU, IRS2, USP8, PIGL, FASN, MYLK2, USP25, EP300 and PPP6R2) and fine-mapped 6 putative causal variants at 6 known PD loci. By combining our results with publicly available eQTL data, we identified 25 putative risk genes in these novel loci whose expression is associated with PD risk. This work lays the groundwork for future efforts aimed at identifying PD loci in non-European populations