10 research outputs found

    Large-Scale Automatic Audiobook Creation

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    An audiobook can dramatically improve a work of literature's accessibility and improve reader engagement. However, audiobooks can take hundreds of hours of human effort to create, edit, and publish. In this work, we present a system that can automatically generate high-quality audiobooks from online e-books. In particular, we leverage recent advances in neural text-to-speech to create and release thousands of human-quality, open-license audiobooks from the Project Gutenberg e-book collection. Our method can identify the proper subset of e-book content to read for a wide collection of diversely structured books and can operate on hundreds of books in parallel. Our system allows users to customize an audiobook's speaking speed and style, emotional intonation, and can even match a desired voice using a small amount of sample audio. This work contributed over five thousand open-license audiobooks and an interactive demo that allows users to quickly create their own customized audiobooks. To listen to the audiobook collection visit \url{https://aka.ms/audiobook}

    Blood stem cell PU.1 upregulation is a consequence of differentiation without fast autoregulation

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    Transcription factors (TFs) regulate cell fates, and their expression must be tightly regulated. Autoregulation is assumed to regulate many TFs' own expression to control cell fates. Here, we manipulate and quantify the (auto)regulation of PU.1, a TF controlling hematopoietic stem and progenitor cells (HSPCs), and correlate it to their future fates.We generate transgenic mice allowing both inducible activation of PU.1 and noninvasive quantification of endogenous PU.1 protein expression. The quantified HSPC PU.1 dynamics show that PU.1 up-regulation occurs as a consequence of hematopoietic differentiation independently of direct fast autoregulation. In contrast, inflammatory signaling induces fast PU.1 up-regulation, which does not require PU.1 expression or its binding to its own autoregulatory enhancer. However, the increased PU.1 levels induced by inflammatory signaling cannot be sustained via autoregulation after removal of the signaling stimulus.We conclude that PU.1 overexpression induces HSC differentiation before PU.1 up-regulation, only later generating cell types with intrinsically higher PU.1.ISSN:0022-1007ISSN:1540-0069ISSN:1540-953

    Yosemite Hydroclimate Network: Distributed Stream and Atmospheric Data for the Tuolumne River Watershed and Surroundings

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    Regions of complex topography and remote wilderness terrain have spatially-varying patterns of temperature and streamflow, but due to inherent difficulties of access, are often very poorly sampled. Here we present a dataset of distributed stream stage, streamflow, stream temperature, barometric pressure, air temperature, and relative humidity from the Tuolumne River Watershed in Yosemite National Park, Sierra Nevada, California, U.S.A. for water years 2002 to 2015, as well as a quality-controlled meteorological forcing timeseries for use in hydrologic modeling. Data unique to this paper were collected using low-visibility and low-impact installations for wilderness locations and can be used alone or as a critical supplement to ancillary datasets collected by cooperating agencies, referenced herein. This dataset provides a unique opportunity to understand spatial patterns and scaling of hydroclimatic processes in complex terrain and can be used to evaluate downscaling techniques or distributed modeling. The paper also provides an example methodology of how to conduct hydroclimatic monitoring in remote wilderness.These data are offered without warranty. Use at your own risk. We ask that you send an e-mail to Jessica Lundquist at jdlund_at_uw.edu if you decide to use the data. Also, please let Jessica know if anything looks odd, as we are continuously trying to improve the data quality control.Funding for data processing came from the National Science Foundation, CBET-0729830, and NASA Grant-NNX15AB29G
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