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The evolutionary history of 2,658 cancers (vol 578, pg 122, 2020)

NATURE 2023年第7948期614卷 E42-E42页

作者： Gerstung, Moritz Jolly, Clemency Leshchiner, Ignaty Dentro, Stefan C. Gonzalez, Santiago Rosebrock, Daniel Mitchell, Thomas J. Rubanova, Yulia Anur, Pavana Yu, Kaixian Tarabichi, Maxime Deshwar, Amit Wintersinger, Jeff Kleinheinz, Kortine Vazquez-Garcia, Ignacio Haase, Kerstin Jerman, Lara Sengupta, Subhajit Macintyre, Geoff Malikic, Salem Donmez, Nilgun Livitz, Dimitri G. Cmero, Marek Demeulemeester, Jonas Schumacher, Steven Fan, Yu Yao, Xiaotong Lee, Juhee Schlesner, Matthias Boutros, Paul C. Bowtell, David D. Zhu, Hongtu Getz, Gad Imielinski, Marcin Beroukhim, Rameen Sahinalp, S. Cenk Ji, Yuan Peifer, Martin Markowetz, Florian Mustonen, Ville Yuan, Ke Wang, Wenyi Morris, Quaid D. Spellman, Paul T. Wedge, David C. Van Loo, Peter European Molecular Biology Laboratory European Bioinformatics Institute (EMBL-EBI) Cambridge UK European Molecular Biology Laboratory Genome Biology Unit Heidelberg Germany Wellcome Sanger Institute Cambridge UK Genome Biology Unit European Molecular Biology Laboratory (EMBL) Heidelberg Germany University of Ljubljana Ljubljana Slovenia The Francis Crick Institute London UK Big Data Institute University of Oxford Oxford UK Wellcome Sanger Institute Wellcome Genome Campus Hinxton UK Big Data Institute Li Ka Shing Centre University of Oxford Oxford UK University of Cambridge Cambridge UK Cambridge University Hospitals NHS Foundation Trust Cambridge UK Department of Applied Mathematics and Theoretical Physics Centre for Mathematical Sciences University of Cambridge Cambridge UK Department of Epidemiology and Biostatistics Memorial Sloan Kettering Cancer Center New York NY USA Department of Statistics Columbia University New York NY USA Department of Haematology University of Cambridge Cambridge UK University of Leuven Leuven Belgium Broad Institute of MIT and Harvard Cambridge MA USA Center for Cancer Research Massachusetts General Hospital Charlestown MA USA Department of Pathology Massachusetts General Hospital Boston MA USA Harvard Medical School Boston MA USA Center for Cancer Research Massachusetts General Hospital Boston MA USA Dana-Farber Cancer Institute Boston MA USA Department of Medical Oncology Dana-Farber Cancer Institute Boston MA USA Department of Cancer Biology Dana-Farber Cancer Institute Boston MA USA Oxford NIHR Biomedical Research Centre Oxford UK Oxford NIHR Biomedical Research Centre University of Oxford Oxford UK University of Toronto Toronto Ontario Canada Vector Institute Toronto Ontario Canada Vector Institute Toronto ON Canada Department of Computer Science University of Toronto Toronto ON Canada Ontario Institute for Cancer Research Toronto Ontario Canada University of California Los Angeles

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Ecological Show Cave and Wild Cave: Negative Binomial Gllvm’s Arthropod Community Modelling

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Procedia Computer Science 2018年 135卷 377-384页

作者： Rezzy Eko Caraka Shamarina Shohaimi Isma Dwi Kurniawan Riki Herliansyah Arif Budiarto Shinta Purnama Sari Bens Pardamean Bioinformatics and Data Science Research Center Bina Nusantara University Department of Statistics Padjadjaran University Indonesia Department of Biology UIN Sunan Gunung Djati Bandung Department of Mathematics Kalimantan Institute of Technology (ITK) Kalimantan Computer Science Department School of Computer Science Bina Nusantara University Jakarta Indonesia 11480 Computer Science Department BINUS Graduate Program – Master of Computer Science Bina Nusantara University Jakarta Indonesia 11480

Ecology is a branch of biology that studies the interaction and relationship between organisms and their environment. Abundance, distribution of organisms and patterns of biodiversity are great interests for many ecologists. One of interesting ecosystems to be studied is a cave. A cave has a typical environment character with a vulnerable ecosystem. Many caves in Indonesia, particularly in Gunungsewu karst area have been developed into tourist objects (show caves) and managed imprudently. Such cave management has potential to harm the environment and leads to ecosystem destruction. Arthropods are the most abundance fauna in cave that play critical roles in maintaining cave ecosystems equilibrium. In the heart of statistical ecology, we need to analyze the differences on Arthropods community and abiotic (climatic-edaphic) parameters among show caves and wild caves. Statistical techniques are needed for the extraction of such information. GLLVM is one method that is able to explain spatial-based information and is particularly suitable for ecology. In this paper, we use negative binomial models to see the differences on spatial patterns of predator and decomposer Arthropods, also characteristic of edaphic and climatic in each cave.

关键词： Ecology GLLVM Negative Binomial Show cave Wild Cave

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Modeling the causal regulatory network by integrating chromatin accessibility and transcriptome data

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National Science Review 2016年第2期3卷 240-251页

作者： Yong Wang Rui Jiang Wing Hung Wong Department of Statistics Department of Biomedical Data ScienceBio-X ProgramStanford University Academy of Mathematics and Systems Science National Center for Mathematics and Interdisciplinary SciencesChinese Academy of Sciences MOE Key Laboratory of Bioinformatics Bioinformatics Division and Center for Synthetic and Systems BiologyTNLISTDepartment of AutomationTsinghua University

Cell packs a lot of genetic and regulatory information through a structure known as chromatin,*** is wrapped around histone proteins and is tightly packed in a remarkable *** express a gene in a specific coding region,the chromatin would open up and DNA loop may be formed by interacting enhancers and ***,the mediator and cohesion complexes,sequence-specific transcription factors,and RNA polymerase Ⅱ are recruited and work together to elaborately regulate the expression *** is in pressing need to understand how the information,about when,where,and to what degree genes should be expressed,is embedded into chromatin structure and gene regulatory *** to large consortia such as Encyclopedia of DNA Elements(ENCODE) and Roadmap Epigenomic projects,extensive data on chromatin accessibility and transcript abundance are available across many tissues and cell *** rich data offer an exciting opportunity to model the causal regulatory ***,we will review the current experimental approaches,foundational data,computational problems,interpretive frameworks,and integrative models that will enable the accurate interpretation of regulatory ***,we will discuss the efforts to organize,analyze,model,and integrate the DNA accessibility data,transcriptional data,and functional genomic regions *** believe that these efforts will eventually help us understand the information flow within the cell and will influence research directions across many fields.

关键词： gene regulatory network open chromatin DNA accessibility transcription factor colocalization statistical model data integration

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Modeling global dynamics from local snapshots with deep generative neural networks

arXiv

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arXiv 2018年

作者： Gigante, Scott Van Dijk, David Moon, Kevin R. Strzalkowski, Alexander Wolf, Guy Krishnaswamy, Smita Computational Biology and Bioinformatics Program Yale University New HavenCT United States Department of Genetics Yale University New HavenCT United States Department of Computer Science Yale University New HavenCT United States Department of Mathematics and Statistics Utah State University LoganUT United States Department of Computer Science Princeton University PrincetonNJ United States Department of Mathematics and Statistics Universitéde Montreacuteal MontéalQC Canada

Complex high dimensional stochastic dynamic systems arise in many applications in the natural sciences and especially biology. However, while these systems are difficult to describe analytically, "snapshot" measurements that sample the output of the system are often available. In order to model the dynamics of such systems given snapshot data, or local transitions, we present a deep neural network framework we call Dynamics Modeling Network or DyMoN. DyMoN is a neural network framework trained as a deep generative Markov model whose next state is a probability distribution based on the current state. DyMoN is trained using samples of current and nextstate pairs, and thus does not require longitudinal measurements. We show the advantage of DyMoN over shallow models such as Kalman filters and hidden Markov models, and other deep models such as recurrent neural networks in its ability to embody the dynamics (which can be studied via perturbation of the neural network) and generate longitudinal hypothetical trajectories. We perform three case studies in which we apply DyMoN to different types of biological systems and extract features of the dynamics in each case by examining the learned model. Copyright © 2018, The Authors. All rights reserved.

关键词： Deep neural networks

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Unsupervised extraction of phenotypes from cancer clinical notes for association studies

arXiv

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arXiv 2019年

作者： Stark, Stefan G. Hyland, Stephanie L. Pradier, Melanie F. Lehmann, Kjong-Van Wicki, Andreas Perez-Cruz, Fernando Vogt, Julia E. Rätsch, Gunnar Computational Biology Program Memorial Sloan Kettering Cancer Center New York United States Tri-Institutional Ph.D. Program in Computational Biology and Medicine Weill Cornell Medicine New York United States Department of Computer Science ETH Zürich Zürich Switzerland Medical Informatics Group University Hospital Zürich Zürich Switzerland Swiss Institute for Bioinformatics Zurich Switzerland Department of Biology ETH Zürich Zürich Switzerland Department of Signal Processing and Information Theory University Carlos III in Madrid Leganés Spain School of Engineering and Applied Sciences Harvard University CambridgeMA United States Department of Biomedicine University of Basel Basel Switzerland Tumorzentrum University Hospital Basel Basel Switzerland Swiss Data Science Center ETH Zürich and EPFL Lausanne Switzerland Department of Mathematics and Computer Science University of Basel Basel Switzerland

The recent adoption of Electronic Health Records (EHRs) by healthcare providers has introduced an important source of data that provides detailed and highly specific insights into patient phenotypes over large cohorts. These datasets, in combination with machine learning and statistical approaches, generate new opportunities for research and clinical care. However, many methods require the patient representations to be in structured formats, while the information in the EHR is often locked in unstructured text designed for human readability. In this work, we develop the methodology to automatically extract clinical features from clinical narratives from large EHR corpora without the need for prior knowledge. We consider medical terms and sentences appearing in clinical narratives as atomic information units. We propose an efficient clustering strategy suitable for the analysis of large text corpora and utilize the clusters to represent information about the patient compactly. Additionally, we define the sentences on ontologic and natural language vocabularies to automatically detect pertinent combinations of concepts present in the corpus, even when an ontology is not available. To demonstrate the utility of our approach, we perform an association study of clinical features with somatic mutation profiles from 4,007 cancer patients and their tumors. We apply the proposed algorithm to a dataset consisting of .65 thousand documents with a total of .3.2 million sentences. After correcting for cancer type and other confounding factors, we identify a total of 340 significant statistical associations between the presence of somatic mutations and clinical features. We annotated these associations according to their novelty and we report several known associations. We also propose 37 plausible, testable hypothesis for associations where the underlying biological mechanism does not appear to be known. These results illustrate that the automated discovery of clinical features

关键词： Diseases

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The recency and geographical origins of the bat viruses ancestral to SARS-CoV and SARS-CoV-2

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Cell 2025年

作者： Pekar, Jonathan E. Lytras, Spyros Ghafari, Mahan Magee, Andrew F. Parker, Edyth Wang, Yu Ji, Xiang Havens, Jennifer L. Katzourakis, Aris Vasylyeva, Tetyana I. Suchard, Marc A. Hughes, Alice C. Hughes, Joseph Rambaut, Andrew Robertson, David L. Dellicour, Simon Worobey, Michael Wertheim, Joel O. Lemey, Philippe Institute of Ecology and Evolution University of Edinburgh Edinburgh United Kingdom Bioinformatics and Systems Biology Graduate Program University of California San Diego La Jolla 92093 CA United States Department of Biomedical Informatics University of California San Diego La Jolla 92093 CA United States Department of Medicine University of California San Diego La Jolla 92093 CA United States Division of Systems Virology Department of Microbiology and Immunology The Institute of Medical Science The University of Tokyo Tokyo Japan Medical Research Council University of Glasgow Centre for Virus Research Glasgow United Kingdom Department of Biology University of Oxford Oxford United Kingdom Department of Human Genetics David Geffen School of Medicine University of California Los Angeles Los Angeles 90095 CA United States Department of Immunology and Microbiology The Scripps Research Institute La Jolla 92037 CA United States Institute of Genomics and Global Health Redeemer's University Osun State Ede Nigeria Department of Computer Science and Engineering University of California San Diego La Jolla 92093 CA United States Department of Mathematics School of Science and Engineering Tulane University New Orleans LA United States Department of Population Health and Disease Prevention University of California Irvine Irvine 92617 CA United States Department of Biostatistics Fielding School of Public Health University of California Los Angeles Los Angeles 90095 CA United States Department of Computational Medicine David Geffen School of Medicine University of California Los Angeles Los Angeles 90095 CA United States School of Biological Sciences University of Hong Kong Hong Kong Hong Kong China Biodiversity Green Development Foundation Beijing China Spatial Epidemiology Lab (SpELL) Université Libre de Bruxelles CP160/12 50 av. FD Roosevelt Bruxelles 1050 Belgium Department of Microbiology Immunology and Transplantation Rega Institute

The emergence of SARS-CoV in 2002 and SARS-CoV-2 in 2019 led to increased sampling of sarbecoviruses circulating in horseshoe bats. Employing phylogenetic inference while accounting for recombination of bat sarbecoviruses, we find that the closest-inferred bat virus ancestors of SARS-CoV and SARS-CoV-2 existed less than a decade prior to their emergence in humans. Phylogeographic analyses show bat sarbecoviruses traveled at rates approximating their horseshoe bat hosts and circulated in Asia for millennia. We find that the direct ancestors of SARS-CoV and SARS-CoV-2 are unlikely to have reached their respective sites of emergence via dispersal in the bat reservoir alone, supporting interactions with intermediate hosts through wildlife trade playing a role in zoonotic spillover. These results can guide future sampling efforts and demonstrate that viral genomic regions extremely closely related to SARS-CoV and SARS-CoV-2 were circulating in horseshoe bats, confirming their importance as the reservoir species for SARS viruses. © 2025 The Authors

关键词： molecular epidemiology phylogeography sarbecoviruses virus evolution

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Using species ranges and macroeconomic data to fill the gap in costs of biological invasions

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Nature ecology & evolution 2025年 2025 May 26页

作者： Ismael Soto Pierre Courtois Arman Pili Enrico Tordoni Eléna Manfrini Elena Angulo Céline Bellard Elizabeta Briski Miloš Buřič Ross N Cuthbert Antonín Kouba Melina Kourantidou Rafael L Macêdo Boris Leroy Phillip J Haubrock Franck Courchamp Brian Leung Faculty of Fisheries and Protection of Waters South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses University of South Bohemia in České Budějovice Vodňany Czech Republic. isma-sa@***. CEE-M University of Montpellier CNRS INRAE Instit Agro Montpellier France. School of Biological Sciences Faculty of Science Monash University Clayton Victoria Australia. Institute for Biochemistry and Biology University of Potsdam Potsdam Germany. Department of Botany Institute of Ecology and Earth Science University of Tartu Tartu Estonia. Université Paris-Saclay CNRS AgroParisTech Ecologie Société Evolution Gif sur Yvette France. Unité Biologie des Organismes et Ecosystèmes Aquatiques (BOREA UMR 8067) Muséum national d'Histoire naturelle Sorbonne Université Université de Caen Normandie CNRS IRD Université des Antilles Paris France. Estación Biológica de Doñana CSIC Seville Spain. GEOMAR Helmholtz-Zentrum für Ozeanforschung Kiel Kiel Germany. Faculty of Fisheries and Protection of Waters South Bohemian Research Center of Aquaculture and Biodiversity of Hydrocenoses University of South Bohemia in České Budějovice Vodňany Czech Republic. Institute for Global Food Security School of Biological Sciences Queen's University Belfast Belfast UK. AMURE University of Western Brittany Plouzané France. Department of Sociology Environmental and Business Economics University of Southern Denmark Esbjerg Denmark. Woods Hole Oceanographic Institution Falmouth MA USA. Marine Policy Center Woods Hole MA USA. Graduate Program in Conservation and Ecotourism Federal University of Rio de Janeiro State Rio de Janeiro Brazil. Leibniz Institute of Freshwater Ecology and Inland Fisheries (IGB) Berlin Germany. Institute of Biology Freie Universität Berlin Berlin Germany. Department of River Ecology and Conservation Senckenberg Research Institute and Natural History Museum Frankfurt Gelnhausen Germany. CAMB Center for Applied Mathematics and Bioinformatics Gulf

Biological invasions threaten global biodiversity, human well-being and economies. Many regional and taxonomic syntheses of monetary costs have been produced recently but with important knowledge gaps owing to uneven geographic and taxonomic research intensity. Here we combine species distribution models, macroeconomic data and the InvaCost database to produce the highest resolution spatio-temporal cost estimates currently available to bridge these gaps. From a subset of 162 invasive species with 'highly reliable' documented costs at the national level, our interpolation focuses on countries that have not reported any costs despite the known presence of invasive species. This analysis demonstrates a substantial underestimation, with global costs potentially estimated to be 1,646% higher for these species than previously recorded. This discrepancy was uneven geographically and taxonomically, respectively peaking in Europe and for plants. Our results showed that damage costs were primarily driven by gross domestic product, human population size, agricultural area and environmental suitability, whereas management expenditure correlated with gross domestic product and agriculture areas. We also found a lag time for damage costs of 46 years, but management spending was not delayed. The methodological predictive approach of this study provides a more complete view of the economic dimensions of biological invasions and narrows the global disparity in invasion cost reporting.

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Correction to: Genes associated with survival of female bovine blastocysts produced in vivo

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Cell and tissue research 2020年第3期382卷 679页

作者： A M Zolini J Block M B Rabaglino G Rincon M Hoelker J J Bromfield D Salilew-Wondim P J Hansen Department of Animal Sciences D.H. Barron Reproductive and Perinatal Biology Research Program and Genetics Institute University of Florida PO Box 110910 Gainesville FL 32611-0910 USA. Zoetis Inc. Kalamazoo MI 49007 USA. Instituto de Investigación en Ciencias de La Salud CONICET Córdoba Argentina. Quantitative Genetics Bioinformatics and Computational Biology Group Department of Applied Mathematics and Computer Science Technical University of Denmark Kemitorvet 2800 Kgs. Lyngby Denmark. Institute of Animal Science Animal Breeding and Husbandry University of Bonn Bonn Germany. Teaching and Research Station Frankenforst Faculty of Agriculture University of Bonn Königswinter Germany. Center of Integrated Dairy Research University of Bonn Bonn Germany. Department of Animal Sciences D.H. Barron Reproductive and Perinatal Biology Research Program and Genetics Institute University of Florida PO Box 110910 Gainesville FL 32611-0910 USA. pjhansen@ufl.edu.

The first error is on page 5. A sentence lists two genes as SCNA1A and SCNA2A but they should be SCN1A and SCN2A.

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Clinical response to azacitidine in MDS is associated with distinct DNA methylation changes in HSPCs

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Nature Communications 2025年第1期16卷 1-20页

作者： Thoms, Julie A. I. Yan, Feng Hampton, Henry R. Davidson, Sarah Joshi, Swapna Saw, Jesslyn Sarowar, Chowdhury H. Lim, Xin Ying Nunez, Andrea C. Kakadia, Purvi M. Bhuyan, Golam Sarower Zou, Xiaoheng Nguyen, Mary Ghodousi, Elaheh S. Koch, Forrest C. Vafaee, Fatemeh Thompson, I. Richard Karimi, Mohammad M. Pickford, Russell Raftery, Mark J. Hough, Sally Buckland, Griselda Bailey, Michelle Ghodke, Yuvaraj Absar, Noorul Vaughan, Lachlin Pasalic, Leonardo Fong, Chun Y. Kenealy, Melita Hiwase, Devendra K. Stoddart, Rohanna I. Mohammed, Soma Lee, Linda Passam, Freda H. Larsen, Stephen R. Spring, Kevin J. Skarratt, Kristen K. Rebeiro, Patricia Presgrave, Peter Stevenson, William S. Ling, Silvia Tiley, Campbell Fuller, Stephen J. Roncolato, Fernando Enjeti, Anoop K. Hoenemann, Dirk Lemech, Charlotte Jolly, Christopher J. Bohlander, Stefan K. Curtis, David J. Wong, Jason W. H. Unnikrishnan, Ashwin Hertzberg, Mark Olivier, Jake Polizzotto, Mark N. Pimanda, John E. School of Biomedical Sciences University of New South Wales Sydney NSW Australia Bioinformatics Division Walter and Eliza Hall Institute of Medical Research Parkville VIC Australia ANU Clinical Hub for Interventional Research (CHOIR) John Curtin School of Medical Research Canberra ACT Australia Kirby Institute University of New South Wales Sydney NSW Australia School of Clinical Medicine University of New South Wales Sydney NSW Australia Australian Centre for Blood Diseases Monash University Melbourne VIC Australia Leukaemia & Blood Cancer Research Unit Department of Molecular Medicine and Pathology Faculty of Medical and Health Sciences The University of Auckland Auckland New Zealand School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney NSW Australia UNSW Data Science Hub University of New South Wales Sydney NSW Australia Comprehensive Cancer Centre School of Cancer and Pharmaceutical Sciences King’s College London London United Kingdom Bioanalytical Mass Spectrometry Facility University of New South Wales Sydney NSW Australia Westmead Hospital Sydney NSW Australia ICPMR Department of Haematology Westmead Hospital Sydney NSW Australia Department of Haematology Austin Health Melbourne VIC Australia Cabrini Hospital Melbourne VIC Australia Department of Haematology Royal Adelaide Hospital Adelaide SA Australia University of New South Wales Sydney NSW Australia Royal North Shore Hospital Sydney NSW Australia Haematology Research Group Heart Research Institute Sydney NSW Australia Institute of Haematology Royal Prince Alfred Hospital Sydney NSW Australia Medical Oncology Group Liverpool Clinical School School of Medicine Western Sydney University and Ingham Institute for Applied Medical Research Liverpool NSW Australia South-West Sydney Clinical Campuses UNSW Medicine & Health Sydney NSW Australia Sydney Medical School Nepean Clinical School Faculty of Medicine and Health University of Sydney

Hypomethylating agents are frontline therapies for myelodysplastic neoplasms (MDS), yet clinical responses remain unpredictable. We conducted a phase 2 trial comparing injectable and oral azacitidine (AZA) administered over one or three weeks per four-week cycle, with the primary objective of investigating whether response is linked to in vivo drug incorporation or DNA hypomethylation. Our findings show that injection results in higher drug incorporation, but lower DNA demethylation per cycle, while global DNA methylation levels in mononuclear cells are comparable between responders and non-responders. However, hematopoietic stem and progenitor cells (HSPCs) from responders exhibit distinct baseline and early treatment-induced CpG methylation changes at regulatory regions linked to tissue patterning, cell migration, and myeloid differentiation. By cycle six—when clinical responses typically emerge—further differential hypomethylation in responder HSPCs suggests marrow adaptation as a driver of improved hematopoiesis. These findings indicate that intrinsic baseline and early drug-induced epigenetic differences in HSPCs may underlie the variable clinical response to AZA in MDS. © The Author(s) 2025.

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Author Correction: The European Reference Genome Atlas: piloting a decentralised approach to equitable biodiversity genomics

npj biodiversity

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npj biodiversity 2024年第1期3卷 31页

作者： Ann M Mc Cartney Giulio Formenti Alice Mouton Diego De Panis Luísa S Marins Henrique G Leitão Genevieve Diedericks Joseph Kirangwa Marco Morselli Judit Salces-Ortiz Nuria Escudero Alessio Iannucci Chiara Natali Hannes Svardal Rosa Fernández Tim De Pooter Geert Joris Mojca Strazisar Jonathan M D Wood Katie E Herron Ole Seehausen Phillip C Watts Felix Shaw Robert P Davey Alice Minotto José M Fernández Astrid Böhne Carla Alegria Tyler Alioto Paulo C Alves Isabel R Amorim Jean-Marc Aury Niclas Backstrom Petr Baldrian Laima Baltrunaite Endre Barta Bertrand BedHom Caroline Belser Johannes Bergsten Laurie Bertrand Helena Bilandija Mahesh Binzer-Panchal Iliana Bista Mark Blaxter Paulo A V Borges Guilherme Borges Dias Mirte Bosse Tom Brown Rémy Bruggmann Elena Buena-Atienza Josephine Burgin Elena Buzan Alessia Cariani Nicolas Casadei Matteo Chiara Sergio Chozas Fedor Čiampor Angelica Crottini Corinne Cruaud Fernando Cruz Love Dalen Alessio De Biase Javier Del Campo Teo Delic Alice B Dennis Martijn F L Derks Maria Angela Diroma Mihajla Djan Simone Duprat Klara Eleftheriadi Philine G D Feulner Jean-François Flot Giobbe Forni Bruno Fosso Pascal Fournier Christine Fournier-Chambrillon Toni Gabaldon Shilpa Garg Carmela Gissi Luca Giupponi Jessica Gomez-Garrido Josefa González Miguel L Grilo Björn Grüning Thomas Guerin Nadege Guiglielmoni Marta Gut Marcel P Haesler Christoph Hahn Balint Halpern Peter W Harrison Julia Heintz Maris Hindrikson Jacob Höglund Kerstin Howe Graham M Hughes Benjamin Istace Mark J Cock Franc Janžekovič Zophonias O Jonsson Sagane Joye-Dind Janne J Koskimäki Boris Krystufek Justyna Kubacka Heiner Kuhl Szilvia Kusza Karine Labadie Meri Lähteenaro Henrik Lantz Anton Lavrinienko Lucas Leclère Ricardo Jorge Lopes Ole Madsen Ghislaine Magdelenat Giulia Magoga Tereza Manousaki Tapio Mappes Joao Pedro Marques Gemma I Martinez Redondo Florian Maumus Shane A McCarthy Hendrik-Jan Megens Jose Melo-Ferreira Sofia L Mendes Matteo Montagna Joao Moreno Mai-Britt Mosbech Mónica Moura Zuzana Musilova Eugene Myers Will J N Genomics Institute University of California Santa Cruz CA USA. anmmccar@ucsc.edu. The Vertebrate Genome Laboratory The Rockefeller University New York NY USA. Department of Biology University of Florence Sesto Fiorentino Italy. InBios-Conservation Genetics Laboratory University of Liege Liege Belgium. Leibniz Institut für Zoo und Wildtierforschung Berlin Germany. Berlin Center for Genomics in Biodiversity Research Berlin Germany. Department of Biology University of Antwerp Antwerp Belgium. Institute of Zoology University of Cologne Cologne Germany. Department of Chemistry Life Sciences and Environmental Sustainability University of Parma Parma Italy. Institute of Evolutionary Biology (CSIC-Universitat Pompeu Fabra) Barcelona Spain. Naturalis Biodiversity Center Leiden The Netherlands. Neuromics Support Facility VIB Center for Molecular Neurology VIB Antwerp Belgium. Neuromics Support Facility Department of Biomedical Sciences University of Antwerp Antwerp Belgium. Tree of Life Wellcome Sanger Institute Hinxton Cambridge UK. School of Biology and Environmental Science University College Dublin Belfield Ireland. Aquatic Ecology & Evolution Institute of Ecology & Evolution University of Bern Bern Switzerland. Department of Fish Ecology & Evolution Eawag Kastanienbaum Switzerland. Department of Biological and Environmental Science University of Jyvaskyla Jyvaskyla Finland. The Earlham Institute Norwich Research Park Norwich UK. Digital Science London UK. Barcelona Supercomputing Center Spanish National Bioinformatics Institute ELIXIR Spain Getafe Spain. Leibniz Institute for the Analysis of Biodiversity Change Museum Koenig Bonn Bonn Germany. CE3C-Centre for Ecology Evolution and Environmental Changes & CHANGE-Global Change and Sustainability Institute Faculdade de Ciências Universidade de Lisboa Campo Grande Lisboa Portugal. Centro Nacional de Análisis Genómico (CNAG) Barcelona Spain. Universitat de Barcelona (UB) Barcelona Spain. CIBIO C

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