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101. JavaGAT Adaptor for UNICORE 6 – Development and Evaluation in the Project AeroGrid

Author

Eifer, Anastasia, Beck-Ratzka, Alexander, Schreiber, Andreas, Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Doug, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Lin, Hai-Xiang, editor, Alexander, Michael, editor, Forsell, Martti, editor, Knüpfer, Andreas, editor, Prodan, Radu, editor, Sousa, Leonel, editor, and Streit, Achim, editor

Published
2010
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102. Requirements for a Provenance Visualization Component

Author

Kunde, Markus, Bergmeyer, Henning, Schreiber, Andreas, Hutchison, David, Series editor, Kanade, Takeo, Series editor, Kittler, Josef, Series editor, Kleinberg, Jon M., Series editor, Mattern, Friedemann, Series editor, Mitchell, John C., Series editor, Naor, Moni, Series editor, Nierstrasz, Oscar, Series editor, Pandu Rangan, C., Series editor, Steffen, Bernhard, Series editor, Sudan, Madhu, Series editor, Terzopoulos, Demetri, Series editor, Tygar, Doug, Series editor, Vardi, Moshe Y., Series editor, Weikum, Gerhard, Series editor, Freire, Juliana, editor, Koop, David, editor, and Moreau, Luc, editor

Published
2008
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103. A Python Library for Provenance Recording and Querying

Author

Bochner, Carsten, Gude, Roland, Schreiber, Andreas, Hutchison, David, Series editor, Kanade, Takeo, Series editor, Kittler, Josef, Series editor, Kleinberg, Jon M., Series editor, Mattern, Friedemann, Series editor, Mitchell, John C., Series editor, Naor, Moni, Series editor, Nierstrasz, Oscar, Series editor, Pandu Rangan, C., Series editor, Steffen, Bernhard, Series editor, Sudan, Madhu, Series editor, Terzopoulos, Demetri, Series editor, Tygar, Doug, Series editor, Vardi, Moshe Y., Series editor, Weikum, Gerhard, Series editor, Freire, Juliana, editor, Koop, David, editor, and Moreau, Luc, editor

Published
2008
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106. miR‐200/375 control epithelial plasticity‐associated alternative splicing by repressing the RNA‐binding protein Quaking

Author

Pillman, Katherine A, Phillips, Caroline A, Roslan, Suraya, Toubia, John, Dredge, B Kate, Bert, Andrew G, Lumb, Rachael, Neumann, Daniel P, Li, Xiaochun, Conn, Simon J, Liu, Dawei, Bracken, Cameron P, Lawrence, David M, Stylianou, Nataly, Schreiber, Andreas W, Tilley, Wayne D, Hollier, Brett G, Khew‐Goodall, Yeesim, Selth, Luke A, Goodall, Gregory J, and Gregory, Philip A

Published
2018
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107. Provenance Implementation in a Scientific Simulation Environment

Author

Kloss, Guy K., Schreiber, Andreas, Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Dough, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Moreau, Luc, editor, and Foster, Ian, editor

Published
2006
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108. Automatic Generation of Wrapper Code and Test Scripts for Problem Solving Environments

Author

Schreiber, Andreas, Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Dough, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Dongarra, Jack, editor, Madsen, Kaj, editor, and Waśniewski, Jerzy, editor

Published
2006
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110. Hypofractionation with simultaneous integrated boost after breast-conserving surgery: Long term results of two phase-II trials

Author

Pfaffendorf, Charlotte, primary, Vonthein, Reinhard, additional, Krockenberger-Ziegler, Katja, additional, Dellas, Kathrin, additional, Schreiber, Andreas, additional, Uhlemann, Dorit, additional, Dinges, Stefan, additional, Würschmidt, Florian, additional, Andreas, Peter, additional, Weinstrauch, Evelyn, additional, Eilf, Kirsten, additional, Rades, Dirk, additional, Höller, Ulrike, additional, Combs, Stephanie E., additional, Kazmierczak, Renata, additional, Fehlauer, Fabian, additional, Schreck, Ulrike, additional, Zimmer, Jörg, additional, Dunst, Jürgen, additional, and Krug, David, additional

Published
2022
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111. RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia

Author

Shanmuganathan, Naranie, primary, Wadham, Carol, additional, Thomson, Daniel, additional, Shahrin, Nur Hezrin, additional, Vignaud, Chloe, additional, Obourn, Vanessa, additional, Chaturvedi, Shalini, additional, Yang, Feng, additional, Feng, Jinghua, additional, Saunders, Verity, additional, Kok, Chung H., additional, Yeung, David, additional, King, Rob M., additional, Kenyon, Rosalie R., additional, Lin, Ming, additional, Wang, Paul, additional, Scott, Hamish, additional, Hughes, Timothy, additional, Schreiber, Andreas W., additional, and Branford, Susan, additional

Published
2022
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114. The Provenance Store prOOst for the Open Provenance Model

Author

Schreiber, Andreas, Ney, Miriam, Wendel, Heinrich, Hutchison, David, editor, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Naor, Moni, editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Doug, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Groth, Paul, editor, and Frew, James, editor

Published
2012
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115. Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations

Author

Drazer, Michael W., Homan, Claire C., Yu, Kai, Cavalcante de Andrade Silva, Marcela, McNeely, Kelsey E., Pozsgai, Matthew J., Acevedo-Mendez, Maria G., Segal, Jeremy P., Wang, Peng, Feng, Jinghua, King-Smith, Sarah L., Kim, Erika, Korotev, Sophia, Lawrence, David M., Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Sood, Raman, Velloso, Elvira D.R.P., Brown, Anna L., Liu, Paul P., and Godley, Lucy A.

Published
2022
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116. The Distributed Engineering Framework TENT

Author

Forkert, Tomas, Kersken, Hans-Peter, Schreiber, Andreas, Strietzel, Martin, Wolf, Klaus, Goos, Gerhard, editor, Hartmanis, Juris, editor, van Leeuwen, Jan, editor, Palma, José M. L. M., editor, Dongarra, Jack, editor, and Hernández, Vicente, editor

Published
2001
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117. Script Wrapper for Software Integration Systems

Author

Fischer, Jochen, Schreiber, Andreas, Strietzel, Martin, Goos, Gerhard, editor, Hartmanis, Juris, editor, van Leeuwen, Jan, editor, Bubak, Marian, editor, Afsarmanesh, Hamideh, editor, Hertzberger, Bob, editor, and Williams, Roy, editor

Published
2000
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118. AMANDA - A Distributed System for Aircraft Design

Author

Kersken, Hans-Peter, Schreiber, Andreas, Strietzel, Martin, Faden, Michael, Ahrem, Regine, Post, Peter, Wolf, Kläus, Beckert, Armin, Gerholt, Thomas, Heinrich, Ralf, Kügeler, Edmund, Goos, Gerhard, editor, Hartmanis, Juris, editor, van Leeuwen, Jan, editor, Bode, Arndt, editor, Ludwig, Thomas, editor, Karl, Wolfgang, editor, and Wismüller, Roland, editor

Published
2000
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123. Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome

Author

Arts, Peer, Garland, Jessica, Byrne, Alicia B., Hardy, Tristan S.E., Babic, Milena, Feng, Jinghua, Wang, Paul, Ha, Thuong, King‐Smith, Sarah L., Schreiber, Andreas W., Crawford, April, Manton, Nick, Moore, Lynette, Barnett, Christopher P., and Scott, Hamish S.

Subjects
Clinical Report, paternal mosaicism, PBX1‐related multisystem congenital anomaly syndrome, phenotype expansion, Clinical Reports, recurrence risk
Abstract

Autosomal dominant (de novo) mutations in PBX1 are known to cause congenital abnormalities of the kidney and urinary tract (CAKUT), with or without extra‐renal abnormalities. Using trio exome sequencing, we identified a PBX1 p.(Arg107Trp) mutation in a deceased one‐day‐old neonate presenting with CAKUT, asplenia, and severe bilateral diaphragmatic thinning and eventration. Further investigation by droplet digital PCR revealed that the mutation had occurred post‐zygotically in the father, with different variant allele frequencies of the mosaic PBX1 mutation in blood (10%) and sperm (20%). Interestingly, the father had subclinical hydronephrosis in childhood. With an expected recurrence risk of one in five, chorionic villus sampling and prenatal diagnosis for the PBX1 mutation identified recurrence in a subsequent pregnancy. The family opted to continue the pregnancy and the second affected sibling was stillborn at 35 weeks, presenting with similar severe bilateral diaphragmatic eventration, microsplenia, and complete sex reversal (46, XY female). This study highlights the importance of follow‐up studies for presumed de novo and low‐level mosaic variants and broadens the phenotypic spectrum of developmental abnormalities caused by PBX1 mutations.

Published
2020

124. Simultaneous Genomic and Metagenomic Analysis for Miscarriage and Stillbirth Further Increases the Diagnostic Utility of Genome Sequencing

Author

Scott, Hamish, primary, Byrne, Alicia, additional, Arriola, Luis, additional, Eshraghi, Leila, additional, Ha, Thuong, additional, Feng, Jinghhua, additional, Babic, Milena, additional, Nguyen, Hung, additional, Ludington, Eleanor, additional, King-Smith, Sarah, additional, Parker, Wendy, additional, Kenyon, Rosalie, additional, Ritchie, Brett, additional, Lipsett, Jillian, additional, Manton, Nick, additional, Khong, T, additional, Moore, Lynette, additional, Arts, Peer, additional, Barnett, Christopher, additional, and Schreiber, Andreas, additional

Published
2022
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126. A genomic autopsy identifies causes of perinatal death and provides options to prevent recurrence

Author

Scott, Hamish, primary, Byrne, Alicia, additional, Arts, Peer, additional, Ha, Thuong, additional, Kassahn, Karin, additional, Pais, Lynn, additional, O’Donnell-Luria, Anne, additional, Babic, Milena, additional, Frank, Mahalia, additional, Feng, Jinghhua, additional, Wang, Paul, additional, Lawrence, David, additional, Eshraghi, Leila, additional, Arriola, Luis, additional, Toubia, John, additional, Nguyen, Hung, additional, Network, Genomic Autopsy Study Research, additional, McGillivray, George, additional, Pinner, Jason, additional, McKenzie, Fiona, additional, Morrow, Rebecca, additional, Lipsett, Jillian, additional, Manton, Nick, additional, Khong, T, additional, Moore, Lynette, additional, Liebelt, Jan, additional, Schreiber, Andreas, additional, King-Smith, Sarah, additional, Hardy, Tristan, additional, Jackson, Matilda, additional, and Barnett, Christopher, additional

Published
2022
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127. Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants

Author

Bournazos, Adam M., primary, Riley, Lisa G., additional, Bommireddipalli, Shobhana, additional, Ades, Lesley, additional, Akesson, Lauren S., additional, Al-Shinnag, Mohammad, additional, Alexander, Stephen I., additional, Archibald, Alison D., additional, Balasubramaniam, Shanti, additional, Berman, Yemima, additional, Beshay, Victoria, additional, Boggs, Kirsten, additional, Bojadzieva, Jasmina, additional, Brown, Natasha J., additional, Bryen, Samantha J., additional, Buckley, Michael F., additional, Chong, Belinda, additional, Davis, Mark R., additional, Dawes, Ruebena, additional, Delatycki, Martin, additional, Donaldson, Liz, additional, Downie, Lilian, additional, Edwards, Caitlin, additional, Edwards, Matthew, additional, Engel, Amanda, additional, Ewans, Lisa J., additional, Faiz, Fathimath, additional, Fennell, Andrew, additional, Field, Michael, additional, Freckmann, Mary-Louise, additional, Gallacher, Lyndon, additional, Gear, Russell, additional, Goel, Himanshu, additional, Goh, Shuxiang, additional, Goodwin, Linda, additional, Hanna, Bernadette, additional, Harraway, James, additional, Higgins, Megan, additional, Ho, Gladys, additional, Hopper, Bruce K., additional, Horton, Ari E., additional, Hunter, Matthew F., additional, Huq, Aamira J., additional, Josephi-Taylor, Sarah, additional, Joshi, Himanshu, additional, Kirk, Edwin, additional, Krzesinski, Emma, additional, Kumar, Kishore R., additional, Lemckert, Frances, additional, Leventer, Richard J., additional, Lindsey-Temple, Suzanna E., additional, Lunke, Sebastian, additional, Ma, Alan, additional, Macaskill, Steven, additional, Mallawaarachchi, Amali, additional, Marty, Melanie, additional, Marum, Justine E., additional, McCarthy, Hugh J., additional, Menezes, Manoj P., additional, McLean, Alison, additional, Milnes, Di, additional, Mohammad, Shekeeb, additional, Mowat, David, additional, Niaz, Aram, additional, Palmer, Elizabeth E., additional, Patel, Chirag, additional, Patel, Shilpan G., additional, Phelan, Dean, additional, Pinner, Jason R., additional, Rajagopalan, Sulekha, additional, Regan, Matthew, additional, Rodgers, Jonathan, additional, Rodrigues, Miriam, additional, Roxburgh, Richard H., additional, Sachdev, Rani, additional, Roscioli, Tony, additional, Samarasekera, Ruvishani, additional, Sandaradura, Sarah A., additional, Savva, Elena, additional, Schindler, Tim, additional, Shah, Margit, additional, Sinnerbrink, Ingrid B., additional, Smith, Janine M., additional, Smith, Richard J., additional, Springer, Amanda, additional, Stark, Zornitza, additional, Strom, Samuel P., additional, Sue, Carolyn M., additional, Tan, Kenneth, additional, Tan, Tiong Y., additional, Tantsis, Esther, additional, Tchan, Michel C., additional, Thompson, Bryony A., additional, Trainer, Alison H., additional, van Spaendonck-Zwarts, Karin, additional, Walsh, Rebecca, additional, Warwick, Linda, additional, White, Stephanie, additional, White, Susan M., additional, Williams, Mark G., additional, Wilson, Meredith J., additional, Wong, Wui Kwan, additional, Wright, Dale C., additional, Yap, Patrick, additional, Yeung, Alison, additional, Young, Helen, additional, Jones, Kristi J., additional, Bennetts, Bruce, additional, Cooper, Sandra T., additional, Abdulrasool, Ghusoon, additional, Al Eryani, Ghamdan, additional, Arts, Peer, additional, Bagnall, Richard, additional, Baker, Naomi L., additional, Barnett, Christopher, additional, Beecroft, Sarah, additional, Berbic, Marina, additional, Black, Michael, additional, Blackburn, Jim, additional, Blombery, Piers, additional, Bournazos, Adam M., additional, Branford, Susan, additional, Breen, Jimmy, additional, Burnett, Leslie, additional, Canson, Daffodil, additional, Cheong, Pak, additional, Chew, Edward, additional, Christodoulou, John, additional, Chung, Seo-Kyung, additional, Clark, Mike, additional, Cliffe, Corrina, additional, Cole, Melissa, additional, Collins, Felicity, additional, Compton, Alison, additional, Cooper, Antony, additional, Corbett, Mark, additional, Cowley, Mark, additional, Dudding, Tracy, additional, Eggers, Stefanie, additional, Eyras, Eduardo, additional, Fernandez, Miriam Fanjul, additional, Fellowes, Andrew, additional, Fleischer, Ron, additional, Folland, Chiara, additional, Fox, Lucy, additional, Gaff, Clara, additional, Galea, Melanie, additional, Ghaoui, Roula, additional, Gornanitis, Ilias, additional, Ha, Thuong, additional, Hayashi, Rippei, additional, Hayes, Ian, additional, Henderson, Alex, additional, Hesson, Luke, additional, Heyer, Erin, additional, Hildebrand, Michael, additional, Hipwell, Michael, additional, Hoskins, Cass, additional, Jackson, Matilda, additional, James, Paul, additional, Wong, Justin Jong-Leong, additional, Kassahn, Karin, additional, Kaub, Peter, additional, Kevin, Lucy, additional, Kumble, Smitha, additional, Kummerfeld, Sarah, additional, Laing, Nigel, additional, Lau, Chiyan, additional, Lee, Eric, additional, Leighton, Sarah, additional, Lundie, Ben, additional, Mayoh, Chelsea, additional, McGaughran, Julie, additional, McPhillips, Mary, additional, Meldrum, Cliff, additional, Middleton, Edwina, additional, Mina, Kym, additional, Nisselle, Amy, additional, Oates, Emily, additional, Oshlack, Alicia, additional, Parasivam, Gayathri, additional, Parsons, Michael, additional, Quinn, Michael, additional, Rasko, John, additional, Ravenscroft, Gina, additional, Ravine, Anja, additional, Recsei, Krista, additional, Rehn, Jacqueline, additional, Robertson, Stephen, additional, Ronan, Anne, additional, Ryland, Georgina, additional, Sadedin, Simon, additional, Schreiber, Andreas, additional, Scott, Hamish, additional, Scott, Rodney, additional, Semsarian, Christopher, additional, Simons, Cas, additional, Singer, Emma, additional, Smyth, Renee, additional, Spurdle, Amanda, additional, Sullivan, Patricia, additional, Sundercombe, Samantha, additional, Thorburn, David, additional, Toubia, John, additional, Trent, Ronald, additional, Tudini, Emma, additional, Voneague, Irina, additional, Waddell, Leigh, additional, Walker, Logan, additional, Wallis, Mathew, additional, Warnock, Nick, additional, Weatheritt, Robert, additional, White, Deborah, additional, Winship, Ingrid, additional, Worgan, Lisa, additional, Wu, Kathy, additional, and Ziolowski, Andrew, additional

Published
2022
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129. Childhood acute myeloid leukemia shows a high level of germline predisposition

Author

Samaraweera, Saumya E., primary, Wang, Paul P. S., additional, Li, Ka Leung, additional, Casolari, Debora A., additional, Feng, Jinghua, additional, Pinese, Mark, additional, Maung, Kyaw Ze Ya, additional, Leo, Paul, additional, Cowley, Mark, additional, Perkins, Kelly, additional, Smith, Amanda M., additional, Ellis, Jonathan, additional, Wee, Amilia, additional, Hiwase, Devendra K., additional, Scott, Hamish S., additional, Schreiber, Andreas W., additional, Brown, Anna L., additional, Deans, Andrew J., additional, Ross, David M., additional, Moore, Andrew S., additional, Gonda, Thomas J., additional, Hahn, Christopher N., additional, and D’Andrea, Richard J., additional

Published
2021
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132. Bots in software engineering: a systematic mapping study

Author

Santhanam, Sivasurya, Hecking, Tobias, Schreiber, Andreas, and Wagner, Stefan

Subjects
Digital assistants, Software engineering, Conversational AI, Bots, BotSE, Electronic computers. Computer science, Human-Computer Interaction Artificial Intelligence Natural Language and Speech Software Engineering, ComputingMilieux_PERSONALCOMPUTING, QA75.5-76.95
Abstract

Bots have emerged from research prototypes to deployable systems due to the recent developments in machine learning, natural language processing and understanding techniques. In software engineering, bots range from simple automated scripts to decision-making autonomous systems. The spectrum of applications of bots in software engineering is so wide and diverse, that a comprehensive overview and categorization of such bots is needed. Existing works considered selective bots to be analyzed and failed to provide the overall picture. Hence it is significant to categorize bots in software engineering through analyzing why, what and how the bots are applied in software engineering. We approach the problem with a systematic mapping study based on the research articles published in this topic. This study focuses on classification of bots used in software engineering, the various dimensions of the characteristics, the more frequently researched area, potential research spaces to be explored and the perception of bots in the developer community. This study aims to provide an introduction and a broad overview of bots used in software engineering. Discussions of the feedback and results from several studies provide interesting insights and prospective future directions.

Published
2021

133. Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy

Author

Ricos, Michael G., Hodgson, Bree L., Pippucci, Tommaso, Saidin, Akzam, Ong, Yeh Sze, Heron, Sarah E., Licchetta, Laura, Bisulli, Francesca, Bayly, Marta A., Hughes, James, Baldassari, Sara, Palombo, Flavia, Santucci, Margherita, Meletti, Stefano, Berkovic, Samuel F., Rubboli, Guido, Thomas, Paul Q., Scheffer, Ingrid E., Tinuper, Paolo, Geoghegan, Joel, Schreiber, Andreas W., and Dibbens, Leanne M.

Published
2016
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145. The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

Author

Homan, Claire C., primary, King-Smith, Sarah L., additional, Lawrence, David M., additional, Arts, Peer, additional, Feng, Jinghua, additional, Andrews, James, additional, Armstrong, Mark, additional, Ha, Thuong, additional, Dobbins, Julia, additional, Drazer, Michael W., additional, Yu, Kai, additional, Bödör, Csaba, additional, Cantor, Alan, additional, Cazzola, Mario, additional, Degelman, Erin, additional, DiNardo, Courtney D., additional, Duployez, Nicolas, additional, Favier, Remi, additional, Fröhling, Stefan, additional, Fitzgibbon, Jude, additional, Klco, Jeffery M., additional, Krämer, Alwin, additional, Kurokawa, Mineo, additional, Lee, Joanne, additional, Malcovati, Luca, additional, Morgan, Neil V., additional, Natsoulis, Georges, additional, Owen, Carolyn, additional, Patel, Keyur P., additional, Preudhomme, Claude, additional, Raslova, Hana, additional, Rienhoff, Hugh, additional, Ripperger, Tim, additional, Schulte, Rachael, additional, Tawana, Kiran, additional, Velloso, Elvira, additional, Yan, Benedict, additional, Liu, Paul, additional, Godley, Lucy A., additional, Schreiber, Andreas W., additional, Hahn, Christopher N., additional, Scott, Hamish S., additional, and Brown, Anna L., additional

Published
2021
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147. Additional file 3 of Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

Author

Angelis, Carla De, Byrne, Alicia B., Morrow, Rebecca, Jinghua Feng, Ha, Thuong, Wang, Paul, Schreiber, Andreas W., Babic, Milena, Taranath, Ajay, Manton, Nick, King-Smith, Sarah L., Quenten Schwarz, Arts, Peer, Scott, Hamish S., and Barnett, Christopher

Abstract

Additional file 3: Figure S3. Conservation of the LAMC3 variants. a The arginine residue at the location of the p.Arg356Cys variant (red box) is highly conserved across 100 species. The introduction of a cysteine at amino acid 356 may disrupt the completely conserved disulphide binding pattern of cysteines (blue boxes) in the region. b The glutamine residue at the location of the p.Gln909Arg variant (red box) is highly conserved across 100 species.

Published
2021
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148. Towards a Collaborative Experimental Environment for Graph Visualization Research in Virtual Reality

Author

Heidrich, David, Meinecke, Annika, and Schreiber, Andreas

Subjects
Collaboration in software development, Collaborative and social computing systems and tools, Collaborative and Social Computing, Collaboration in Software Engineering, Software and its engineering, Human centered computing, Interaction techniques, Virtual reality, Graph drawings
Abstract

Graph visualization benefit from virtual reality (VR) technology and a collaborative environment. However, implementing collaborative graph visualizations can be very resource consuming and existing prototypes cannot be reused easily. We present a work-in-progress collaborative experimental environment for graph visualization research in VR, which is highly modular, contains all fundamental functionality of a collaborative graph visualization, and provides common interaction techniques. Our environment enables researchers to create and evaluate modules in the same environment for a wide range of experiments., EuroVis 2021 - Posters, Posters, 9, 11, David Heidrich, Annika Meinecke, and Andreas Schreiber, CCS Concepts: Human-centered computing --> Virtual reality; Graph drawings; Interaction techniques; Collaborative and social computing systems and tools; Software and its engineering --> Collaboration in software development

Published
2021
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150. Additional file 2 of Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia

Author

Angelis, Carla De, Byrne, Alicia B., Morrow, Rebecca, Jinghua Feng, Ha, Thuong, Wang, Paul, Schreiber, Andreas W., Babic, Milena, Taranath, Ajay, Manton, Nick, King-Smith, Sarah L., Quenten Schwarz, Arts, Peer, Scott, Hamish S., and Barnett, Christopher

Abstract

Additional file 2: Figure S2. Family pedigree and segregation of the LAMC3 variants by Sanger sequencing. Both LAMC3 variants were confirmed to be present in compound heterozygosity in the proband. The paternal variant, p.Arg356Cys, and the maternal variant, p.Gln909Arg, were confirmed as heterozygous. Only the paternal variant was present in unaffected sibling 1, and only the maternal variant was present in the current unaffected pregnancy. The third unaffected sibling carries neither variant.

Published
2021
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