The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research [version 1; peer review: 2 approved] von Salgado, David, Armean, Irina M, Baudis, Michael, Beltran, Sergi, Capella-Gutierrez, Salvador, Carvalho-Silva, Denise, Dominguez Del Angel, Victoria, Dopazo, Joaquin, Furlong, Laura I, Gao, Bo, Garcia, Leyla, Gerloff, Dietlind, Gut, Ivo, Gyenesei, Attila, Habermann, Nina, Hancock, John M, Hanauer, Marc, Hovig, Eivind, Johansson, Lennart F, Keane, Thomas, Korbel, Jan, Lauer, Katharina B, Laurie, Steve, Leskošek, Brane, Lloyd, David, Marques-Bonet, Tomas, Mei, Hailiang, Monostory, Katalin, Piñero, Janet, Poterlowicz, Krzysztof, Rath, Ana, Samarakoon, Pubudu, Sanz, Ferran, Saunders, Gary, Sie, Daoud, Swertz, Morris A, Tsukanov, Kirill, Valencia, Alfonso, Vidak, Marko, Yenyxe González, Cristina, Ylstra, Bauke, Béroud, Christophe

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The Human Phenotype Ontology in 2021 von Köhler, Sebastian, Gargano, Michael, Matentzoglu, Nicolas, Carmody, Leigh C, Lewis-Smith, David, Vasilevsky, Nicole A, Danis, Daniel, Balagura, Ganna, Baynam, Gareth, Brower, Amy M, Callahan, Tiffany J, Chute, Christopher G, Est, Johanna L, Galer, Peter D, Ganesan, Shiva, Griese, Matthias, Haimel, Matthias, Pazmandi, Julia, Hanauer, Marc, Harris, Nomi L, Hartnett, Michael J, Hastreiter, Maximilian, Hauck, Fabian, He, Yongqun, Jeske, Tim, Kearney, Hugh, Kindle, Gerhard, Klein, Christoph, Knoflach, Katrin, Krause, Roland, Lagorce, David, McMurry, Julie A, Miller, Jillian A, Munoz-Torres, Monica C, Peters, Rebecca L, Rapp, Christina K, Rath, Ana M, Rind, Shahmir A, Rosenberg, Avi Z, Segal, Michael M, Seidel, Markus G, Smedley, Damian, Talmy, Tomer, Thomas, Yarlalu, Wiafe, Samuel A, Xian, Julie, Yüksel, Zafer, Helbig, Ingo, Mungall, Christopher J, Haendel, Melissa A, Robinson, Peter N

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Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources von Köhler, Sebastian, Carmody, Leigh, Vasilevsky, Nicole, Jacobsen, Julius O B, Danis, Daniel, Gourdine, Jean-Philippe, Gargano, Michael, Harris, Nomi L, Matentzoglu, Nicolas, McMurry, Julie A, Osumi-Sutherland, David, Cipriani, Valentina, Balhoff, James P, Conlin, Tom, Blau, Hannah, Baynam, Gareth, Palmer, Richard, Gratian, Dylan, Dawkins, Hugh, Segal, Michael, Jansen, Anna C, Muaz, Ahmed, Chang, Willie H, Bergerson, Jenna, Laulederkind, Stanley J F, Yüksel, Zafer, Beltran, Sergi, Freeman, Alexandra F, Sergouniotis, Panagiotis I, Durkin, Daniel, Storm, Andrea L, Hanauer, Marc, Brudno, Michael, Bello, Susan M, Sincan, Murat, Rageth, Kayli, Wheeler, Matthew T, Oegema, Renske, Lourghi, Halima, Della Rocca, Maria G, Thompson, Rachel, Castellanos, Francisco, Priest, James, Cunningham-Rundles, Charlotte, Hegde, Ayushi, Lovering, Ruth C, Hajek, Catherine, Olry, Annie, Notarangelo, Luigi, Similuk, Morgan, Zhang, Xingmin A, Gómez-Andrés, David, Lochmüller, Hanns, Dollfus, Hélène, Rosenzweig, Sergio, Marwaha, Shruti, Rath, Ana, Sullivan, Kathleen, Smith, Cynthia, Milner, Joshua D, Leroux, Dorothée, Boerkoel, Cornelius F, Klion, Amy, Carter, Melody C, Groza, Tudor, Smedley, Damian, Haendel, Melissa A, Mungall, Chris, Robinson, Peter N

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The Human Phenotype Ontology in 2024: phenotypes around the world von Gargano, Michael A, Matentzoglu, Nicolas, Coleman, Ben, Bagley, Anita M, Balhoff, James P, Bertram, Holli, Botas, Pablo, Cameron, Rhiannon, Caufield, J Harry, Chute, Christopher G, Dahan-Oliel, Noémi, Davids, Jon R, de Dieuleveult, Maud, de Souza, Vinicius, Derfalvi, Beata, Diaz-Byrd, Claudia, Dingemans, Alexander J M, Fabrizzi, Carolina, Fico, Giovanna, Firth, Helen V, Fullerton, Janice M, Gabriel, Davera L, Goes, Fernando S, Moses, Rachel Gore, Griese, Matthias, Gu, Weihong, Guthrie, Julia, Hamosh, Ada, Hanauer, Marc, Hanušová, Kateřina, He, Yongqun (Oliver), Hegde, Harshad, Helbig, Ingo, Holasová, Kateřina, Hurwitz, Eric, Jiang, Xiaofeng, Joseph, Lisa, King, Bryan, Knoflach, Katrin, Koolen, David A, Ladewig, Markus S, Lagorce, David, Lai, Meng-Chuan, Lapunzina, Pablo, Lewis-Smith, David, Li, Xiarong, Lucano, Caterina, Majd, Marzieh, Marazita, Mary L, Millett, Caitlin E, Mitchell, Philip B, Narutomi, Kenji, Nematollahi, Shahrzad, Ogishima, Soichi, Ortiz, Abigail, Pachajoa, Harry, Peters, Amy, Putman, Tim, Rapp, Christina K, Rath, Ana, Rekerle, Lauren, Roy, Suzy, Sanders, Stephan J, Schuetz, Catharina, Schulte, Eva C, Schulze, Thomas G, Seelow, Dominik, Seitz, Berthold, Similuk, Morgan N, Simon, Eric S, Singh, Balwinder, Smith, Cynthia L, Smolinsky, Jake T, Sperry, Sarah, Steinhaus, Robin, Sundaramurthi, Jagadish Chandrabose, Tenorio Castano, Jair A, Tesner, Pavel, Thomas, Rhys H, Thurm, Audrey, Turnovec, Marek, van Gijn, Marielle E, Vlčková, Markéta, Walden, Anita, Wiafe, Samuel A, Wiggins, Lisa D, Wu, Chen, Xiong, Hui, Yalin, Nefize, Yamamoto, Yasunori, Yatham, Lakshmi N, Young, Allan H, Yüksel, Zafer, Zankl, Andreas, Toro, Sabrina, Carmody, Leigh C, Harris, Nomi L, Munoz-Torres, Monica C, Köhler, Sebastian, Robinson, Peter N

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The ELIXIR Core Data Resources: fundamental infrastructure for the life sciences von Drysdale, Rachel, Cook, Charles E, Petryszak, Robert, Baillie-Gerritsen, Vivienne, Barlow, Mary, Gasteiger, Elisabeth, Gruhl, Franziska, Haas, Jürgen, Lanfear, Jerry, Lopez, Rodrigo, Redaschi, Nicole, Stockinger, Heinz, Teixeira, Daniel, Venkatesan, Aravind, Blomberg, Niklas, Durinx, Christine, McEntyre, Johanna

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Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases von Zurek, Birte, Ellwanger, Kornelia, Vissers, Lisenka E L M, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, de Voer, Richarda M, Laurie, Steven, Matalonga, Leslie, Gilissen, Christian, Ossowski, Stephan, 't Hoen, Peter A C, Vitobello, Antonio, Schulze-Hentrich, Julia M, Riess, Olaf, Brunner, Han G, Brookes, Anthony J, Rath, Ana, Bonne, Gisèle, Gumus, Gulcin, Verloes, Alain, Hoogerbrugge, Nicoline, Evangelista, Teresinha, Harmuth, Tina, Swertz, Morris, Spalding, Dylan, Hoischen, Alexander, Beltran, Sergi, Graessner, Holm

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Solving patients with rare diseases through programmatic reanalysis of genome-phenome data von Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E L M, de Voer, Richarda, Tonda, Raul, Laurie, Steven, Fernandez-Callejo, Marcos, Picó, Daniel, Garcia-Linares, Carles, Papakonstantinou, Anastasios, Corvó, Alberto, Joshi, Ricky, Diez, Hector, Gut, Ivo, Hoischen, Alexander, Graessner, Holm, Beltran, Sergi

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Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report von Lagorce, David, Lebreton, Emeline, Matalonga, Leslie, Hongnat, Oscar, Chahdil, Maroua, Piscia, Davide, Paramonov, Ida, Ellwanger, Kornelia, Köhler, Sebastian, Robinson, Peter, Graessner, Holm, Beltran, Sergi, Lucano, Caterina, Hanauer, Marc, Rath, Ana

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Phenotypic similarity-based approach for variant prioritization for unsolved rare disease: a preliminary methodological report von Lagorce, David, Lebreton, Emeline, Matalonga, Leslie, Hongnat, Oscar, Chahdil, Maroua, Piscia, Davide, Paramonov, Ida, Ellwanger, Kornelia, Köhler, Sebastian, Robinson, Peter N, Graessner, Holm, Beltran, Sergi, Lucano, Caterina, Hanauer, Marc, Rath, Ana

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Solving unsolved rare neurological diseases-a Solve-RD viewpoint von Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E, Reichbauer, Jennifer, Wayand, Melanie, van de Warrenburg, Bart, Schöls, Ludger, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis

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Harmonising phenomics information for a better interoperability in the rare disease field von Maiella, Sylvie, Olry, Annie, Hanauer, Marc, Lanneau, Valérie, Lourghi, Halima, Donadille, Bruno, Rodwell, Charlotte, Köhler, Sebastian, Seelow, Dominik, Jupp, Simon, Parkinson, Helen, Groza, Tudor, Brudno, Michael, Robinson, Peter N., Rath, Ana

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Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data von Matalonga, Leslie, Hernández-Ferrer, Carles, Piscia, Davide, Cohen, Enzo, Cuesta, Isabel, Danis, Daniel, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Gilissen, Christian, Johari, Mridul, Laurie, Steven, Li, Shuang, Nelson, Isabelle, Peters, Sophia, Paramonov, Ida, Prasanth, Sivakumar, Robinson, Peter, Sablauskas, Karolis, Savarese, Marco, Steyaert, Wouter, van der Velde, Joeri K., Vitobello, Antonio, Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, Vissers, Lisenka E. L. M., de Voer, Richarda, Aretz, Stefan, Capella, Gabriel, de Voer, Richarda M., Evans, Gareth, Pelaez, Jose Garcia, Holinski-Feder, Elke, Hoogerbrugge, Nicoline, Laner, Andreas, Oliveira, Carla, Rump, Andreas, Schröck, Evelin, Sommer, Anna Katharina, Steinke-Lange, Verena, Paske, Iris te, Tischkowitz, Marc, Valle, Laura, Banka, Siddharth, Benetti, Elisa, Casari, Giorgio, Ciolfi, Andrea, Clayton-Smith, Jill, Dallapiccola, Bruno, de Boer, Elke, Ellwanger, Kornelia, Faivre, Laurence, Graessner, Holm, Haack, Tobias B., Hammarsjö, Anna, Havlovicova, Marketa, Hoischen, Alexander, Hugon, Anne, Jackson, Adam, Kleefstra, Tjitske, Lindstrand, Anna, López-Martín, Estrella, Macek, Milan, Morleo, Manuela, Nigro, Vicenzo, Nordgren, Ann, Pettersson, Maria, Pinelli, Michele, Pizzi, Simone, Posada, Manuel, Radio, Francesca Clementina, Renieri, Alessandra, Rooryck, Caroline, Ryba, Lukas, Schwarz, Martin, Tartaglia, Marco, Thauvin, Christel, Torella, Annalaura, Trimouille, Aurélien, Verloes, Alain, Vissers, Lisenka, Votypka, Pavel, Vyshka, Klea, Zurek, Birte, Baets, Jonathan, Beijer, Danique, Bonne, Gisèle, Cossins, Judith, Evangelista, Teresinha, Ferlini, Alessandra, Hackman, Peter, Hanna, Michael G., Horvath, Rita, Houlden, Henry, Lau, Jarred, Lochmüller, Hanns, Macken, William L., Musacchia, Francesco, Nascimento, Andres, Natera-de Benito, Daniel

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Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases von Zurek, Birte, Ellwanger, Kornelia, Vissers, Lisenka E. L. M., Schüle, Rebecca, Synofzik, Matthis, Töpf, Ana, de Voer, Richarda M., Laurie, Steven, Matalonga, Leslie, Gilissen, Christian, Ossowski, Stephan, ’t Hoen, Peter A. C., Vitobello, Antonio, Schulze-Hentrich, Julia M., Riess, Olaf, Brunner, Han G., Brookes, Anthony J., Rath, Ana, Bonne, Gisèle, Gumus, Gulcin, Verloes, Alain, Hoogerbrugge, Nicoline, Evangelista, Teresinha, Harmuth, Tina, Swertz, Morris, Spalding, Dylan, Hoischen, Alexander, Beltran, Sergi, Graessner, Holm, Haack, Tobias B., Zurek, Birte, Ellwanger, Kornelia, Demidov, German, Sturm, Marc, Kessler, Christoph, Wayand, Melanie, Wilke, Carlo, Traschütz, Andreas, Schöls, Ludger, Hengel, Holger, Heutink, Peter, Brunner, Han, Scheffer, Hans, Steyaert, Wouter, Sablauskas, Karolis, de Voer, Richarda M., Kamsteeg, Erik-Jan, van de Warrenburg, Bart, van Os, Nienke, te Paske, Iris, Janssen, Erik, de Boer, Elke, Steehouwer, Marloes, Yaldiz, Burcu, Kleefstra, Tjitske, Veal, Colin, Gibson, Spencer, Wadsley, Marc, Mehtarizadeh, Mehdi, Riaz, Umar, Warren, Greg, Dizjikan, Farid Yavari, Shorter, Thomas, Straub, Volker, Bettolo, Chiara Marini, Specht, Sabine, Clayton-Smith, Jill, Banka, Siddharth, Alexander, Elizabeth, Jackson, Adam, Faivre, Laurence, Thauvin, Christel, Vitobello, Antonio, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Tisserant, Emilie, Bruel, Ange-Line, Peyron, Christine, Pélissier, Aurore, Beltran, Sergi, Gut, Ivo Glynne, Laurie, Steven, Piscia, Davide, Papakonstantinou, Anastasios, Bullich, Gemma, Corvo, Alberto, Garcia, Carles, Fernandez-Callejo, Marcos, Hernández, Carles, Picó, Daniel, Paramonov, Ida, Lochmüller, Hanns, Bros-Facer, Virginie, Hanauer, Marc, Olry, Annie, Lagorce, David, Havrylenko, Svitlana, Izem, Katia, Rigour, Fanny, Stevanin, Giovanni

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Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint von Schüle, Rebecca, Timmann, Dagmar, Erasmus, Corrie E., Reichbauer, Jennifer, Wayand, Melanie, Baets, Jonathan, Balicza, Peter, Chinnery, Patrick, Dürr, Alexandra, Haack, Tobias, Hengel, Holger, Horvath, Rita, Houlden, Henry, Kamsteeg, Erik-Jan, Kamsteeg, Christoph, Lohmann, Katja, Macaya, Alfons, Marcé-Grau, Anna, Maver, Ales, Molnar, Judit, Münchau, Alexander, Peterlin, Borut, Riess, Olaf, Schöls, Ludger, Stevanin, Giovanni, Synofzik, Matthis, Timmerman, Vincent, van de Warrenburg, Bart, van Os, Nienke, Vandrovcova, Jana, Wilke, Carlo, Wilke, Carlo, Bevot, Andrea, Zuchner, Stephan, Beltran, Sergi, Laurie, Steven, Matalonga, Leslie, Graessner, Holm, Synofzik, Matthis, Graessner, Holm, Zurek, Birte, Ellwanger, Kornelia, Ossowski, Stephan, Demidov, German, Sturm, Marc, Schulze-Hentrich, Julia M., Heutink, Peter, Brunner, Han, Scheffer, Hans, Hoogerbrugge, Nicoline, Hoischen, Alexander, ’t Hoen, Peter A. C., Vissers, Lisenka E. L. M., Gilissen, Christian, Steyaert, Wouter, Sablauskas, Karolis, de Voer, Richarda M., Janssen, Erik, de Boer, Elke, Steehouwer, Marloes, Yaldiz, Burcu, Kleefstra, Tjitske, Brookes, Anthony J., Veal, Colin, Gibson, Spencer, Wadsley, Marc, Mehtarizadeh, Mehdi, Riaz, Umar, Warren, Greg, Dizjikan, Farid Yavari, Shorter, Thomas, Töpf, Ana, Straub, Volker, Bettolo, Chiara Marini, Specht, Sabine, Clayton-Smith, Jill, Banka, Siddharth, Alexander, Elizabeth, Jackson, Adam, Faivre, Laurence, Thauvin, Christel, Vitobello, Antonio, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Tisserant, Emilie, Bruel, Ange-Line, Peyron, Christine, Pélissier, Aurore, Beltran, Sergi, Gut, Ivo Glynne, Laurie, Steven, Piscia, Davide, Papakonstantinou, Anastasios, Bullich, Gemma, Corvo, Alberto, Garcia, Carles, Fernandez-Callejo, Marcos, Hernández, Carles, Picó, Daniel, Paramonov, Ida

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Twist exome capture allows for lower average sequence coverage in clinical exome sequencing von Yaldiz, Burcu, Kucuk, Erdi, Hampstead, Juliet, Hofste, Tom, Pfundt, Rolph, Corominas Galbany, Jordi, Rinne, Tuula, Yntema, Helger G, Hoischen, Alexander, Nelen, Marcel, Gilissen, Christian

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Twist exome capture allows for lower average sequence coverage in clinical exome sequencing von Hampstead, Juliet, Yntema, Helger G, Nelen, Marcel, Haack, Tobias B, Graessner, Holm, Zurek, Birte, Demidov, German, Schulze-Hentrich, Julia M, Wayand, Melanie, Synofzik, Matthis, Traschütz, Andreas, Schöls, Ludger, Lerche, Holger, Scheffer, Hans, Vissers, Lisenka E. L. M, Steyaert, Wouter, de Voer, Richarda M, Kamsteeg, Erik-Jan, van Os, Nienke, te Paske, Iris, Steehouwer, Marloes, Kleefstra, Tjitske, Mehtarizadeh, Mehdi, Shorter, Thomas, Töpf, Ana, Engelhardt, Karin, Clayton-Smith, Jill, Banka, Siddharth, Denommé-Pichon, Anne-Sophie, Bruel, Ange-Line, Peyron, Christine, Gut, Ivo Glynne, Matalonga, Leslie, Bullich, Gemma, Corvo, Alberto, Hongnat, Oscar, Chahdil, Maroua, Stevanin, Giovanni, Davoine, Claire-Sophie, Heinzmann, Anna, Metay, Corinne, Cohen, Enzo, Stojkovic, Tanya, Thomasová, Dana, Parkinson, Helen, Keane, Thomas, Freeberg, Mallory, Thomas, Coline, Robinson, Peter, Costa, Alessia, Reilly, Mary, Cali, Elisa, Muntoni, Francesco, Timmerman, Vincent, Beijer, Danique, Weckhuysen, Sarah, Morleo, Manuela, Varavallo, Alessandra, Ferlini, Alessandra, Bigoni, Stefania, Spier, Isabel, Sommer, Anna Katharina, Peters, Sophia, Gullo, Irene, Swertz, Morris A, Johansson, Lennart, Neerincx, Pieter B, Ruvolo, David, Abbott, Kristin M, Frederikse, Wilhemina SKerstjens, Roelofs-Prins, Dieuwke, Keren, Boris, Lacombe, Didier, De la Paz, Manuel Posada, Ciolfi, Andrea, Pizzi, Simone, Radio, Francesca Clementina, Furini, Simone, Münchau, Alexander, Lohmann, Katja, Macaya, Alfons, Cazurro-Gutiérrez, Ana, Osorio, Andrés Nascimento, Udd, Bjarne, Chinnery, Patrick F, Ratnaike, Thiloka, Schon, Katherine, Başak, Ayşe Nazlı, Dermaut, Bart, Balestrini, Simona, Claeys, Kristl, Bijlsma, Emilia K, Ruivenkamp, Claudia A. L, Haimel, Matthias, Zaganas, Ioannis, Riva, Antonella, Uva, Paolo, Scala, Marcello, Scudieri, Paolo, Solve-RD consortium, [missing]

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An interconnected data infrastructure to support large-scale rare disease research von Johansson, Lennart F, Laurie, Steve, Spalding, Dylan, Gibson, Spencer, Ruvolo, David, Thomas, Coline, Piscia, Davide, de Andrade, Fernanda, Been, Gerieke, Bijlsma, Marieke, Brunner, Han, Cimerman, Sandi, Dizjikan, Farid Yavari, Ellwanger, Kornelia, Fernandez, Marcos, Freeberg, Mallory, van de Geijn, Gert-Jan, Kanninga, Roan, Maddi, Vatsalya, Mehtarizadeh, Mehdi, Neerincx, Pieter, Ossowski, Stephan, Rath, Ana, Roelofs-Prins, Dieuwke, Stok-Benjamins, Marloes, van der Velde, K Joeri, Veal, Colin, van der Vries, Gerben, Wadsley, Marc, Warren, Gregory, Zurek, Birte, Keane, Thomas, Graessner, Holm, Beltran, Sergi, Swertz, Morris A, Brookes, Anthony J

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Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources von Köhler, Sebastian, Carmody, Leigh, Vasilevsky, Nicole, Jacobsen, Julius O.B, Danis, Daniel, Gourdine, Jean Philippe, Gargano, Michael, Harris, Nomi L, Matentzoglu, Nicolas, McMurry, Julie A, Osumi-Sutherland, David, Cipriani, Valentina, Balhoff, James P, Conlin, Tom, Blau, Hannah, Baynam, Gareth, Palmer, Richard, Gratian, Dylan, Dawkins, Hugh, Segal, Michael, Jansen, Anna C, Muaz, Ahmed, Chang, Willie H, Bergerson, Jenna, Laulederkind, Stanley J.F, Yüksel, Zafer, Beltran, Sergi, Freeman, Alexandra F, Sergouniotis, Panagiotis I, Durkin, Daniel, Storm, Andrea L, Hanauer, Marc, Brudno, Michael, Bello, Susan M, Sincan, Murat, Rageth, Kayli, Wheeler, Matthew T, Oegema, Renske, Lourghi, Halima, Della Rocca, Maria G, Thompson, Rachel, Castellanos, Francisco, Priest, James, Cunningham-Rundles, Charlotte, Hegde, Ayushi, Lovering, Ruth C, Hajek, Catherine, Olry, Annie, Notarangelo, Luigi, Similuk, Morgan, Zhang, Xingmin A, Gómez-Andrés, David, Lochmüller, Hanns, Dollfus, Hélène, Rosenzweig, Sergio, Marwaha, Shruti, Rath, Ana, Sullivan, Kathleen, Smith, Cynthia, Milner, Joshua D, Leroux, Dorothée, Boerkoel, Cornelius F, Klion, Amy, Carter, Melody C, Groza, Tudor, Smedley, Damian, Haendel, Melissa A, Mungall, Chris, Robinson, Peter N

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Building Expertise on FAIR Through Evolving Bring Your Own Data (BYOD) Workshops: Describing the Data, Software, and Management-focused Approaches and Their Evolution von Bernabé, César H, Thielemans, Lieze, Kaliyaperumal, Rajaram, Carta, Claudio, Zhang, Shuxin, van Gelder, Celia W.G, Benis, Nirupama, Santos, Luiz Olavo Bonino da Silva, Cornet, Ronald, Vieira, Bruna Dos Santos, Lalout, Nawel, Henriques, Ines, Ballesteros, Alberto Cámara, Burger, Kees, Kersloot, Martijn G, Ehrhart, Friederike, Enckevort, Esther van, Evelo, Chris T, Gray, Alasdair J.G, Hanauer, Marc, Hettne, Kristina, Ligt, Joep de, Pereira, Arnaldo, Queralt-Rosinach, Núria, Schultes, Erik, Taruscio, Domenica, Waagmeester, Andra, Wilkinson, Mark D, Willighagen, Egon L, Jansen, Mascha, Mons, Barend, Roos, Marco, Jacobsen, Annika

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Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources von Köhler, Sebastian, Carmody, Leigh, Vasilevsky, Nicole, Jacobsen, Julius O B, Danis, Daniel, Gourdine, Jean-Philippe, Gargano, Michael, Harris, Nomi L., Matentzoglu, Nicolas, McMurry, Julie A., Osumi-Sutherland, David, Cipriani, Valentina, Balhoff, James P., Conlin, Tom, Blau, Hannah, Baynam, Gareth, Palmer, Richard, Gratian, Dylan, Dawkins, Hugh, Segal, Michael, Jansen, Anna C., Muaz, Ahmed, Chang, Willie H., Bergerson, Jenna, Laulederkind, Stanley J F, Yüksel, Zafer, Beltran, Sergi, Freeman, Alexandra F., Sergouniotis, Panagiotis I., Durkin, Daniel, Storm, Andrea L., Hanauer, Marc, Brudno, Michael, Bello, Susan M., Sincan, Murat, Rageth, Kayli, Wheeler, Matthew T., Oegema, Renske, Lourghi, Halima, Della Rocca, Maria G., Thompson, Rachel, Castellanos, Francisco, Priest, James, Cunningham-Rundles, Charlotte, Hegde, Ayushi, Lovering, Ruth C., Hajek, Catherine, Olry, Annie, Notarangelo, Luigi, Similuk, Morgan, Zhang, Xingmin A., Gómez-Andrés, David, Lochmüller, Hanns, Dollfus, Hélène, Rosenzweig, Sergio, Marwaha, Shruti, Rath, Ana, Sullivan, Kathleen, Smith, Cynthia, Milner, Joshua D., Leroux, Dorothée, Boerkoel, Cornelius F., Klion, Amy, Carter, Melody C., Groza, Tudor, Smedley, Damian, Haendel, Melissa A., Mungall, Chris, Robinson, Peter N.

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