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- HLA Twin software: How to use it and its main functions
- How to review and troubleshoot challenging samples in NanoTYPER
- Learn how NanoTYPE MONO will help you with single locus testing
- Measuring donor-derived cell-free DNA in your laboratory using HoloGRAFT
- NanoTYPER 2.0.0 Spotlight: Embrace the Newest Software Features and Enhancements in our Exclusive Webinar!
- What’s New in NanoTYPER 2.1.0: Unveiling Exciting Features & Improvements
2020
Ariella Sasson, Efi Melista, Ming-shan Chien: High Throughput HLA Typing in the Cloud: How to Make it Rain Genotypes
2019
Kirk J. Mantione, Efi Melista: Automated Library Preparation for HLA Testing Using the Omixon Holotype HLA Kit (24/11) on the Eppendorf epMotion 5075t
J. Kralova, M. Pisacka, H. Cechova, M. Vrana, S. Pubalova, A. Pejchalova, L. Kolesar, M. L. Olsson, B. Hosseini-Maaf: ABO Chimerism as a Limitation of Routine Genotyping Methods
Vera Siffnerova, Kirk Mantione, Efi Melista: Automating Holotype HLA on Eppendorf's Epmotion Liquid Handler and Validating it for Routine HLA Genotyping
Libor Kolesár, Tünde Vágó, Gergely Tölgyesi, Efi Melista: Evaluation of Omixon Holotype HLA on the iSeq 100 Instrument
Nina Lauterbach, Efi Melista, Antonio Martinho: High Throughput HLA Typing Using NGS with Semi-automated Workflow
Valia Bravo-Egana, Collin Brack, Barbara Ure, Renata Santos, Maggi Woronkowicz, Efi Melista, Michael Reardon: Interfacing a Next Generation Sequencing Bioinformatic Pipeline with a Laboratory Information Management System for Use with High Resolution Typing Results and Reporting
Mette Christiansen, Andreas Schimanski, Matthas Niemann, Nina Lauterbach, Efi Melista, Bjarne Kuno Moller, Pernille Bundgaard Koefoed-Nielsen: Donor Selecton for Solid Organ Transplantation Guided by NGS High Resolution HLA Typing in Combination with PIRCHE
Mette Christiansen, Sonja Verheyden, Andreas Schimanski, Matthias Niemann, Nina Lauterbach, Efi Melista, Betina Sorensen, Bjarne Kuno Moller, Christian Demanet: NGS High Resolution Typing in Combination with PIRCHE as a Tool to Select a Permissible HSCT Donor
Elena Shagimardanova, Yana Leksina, Regina Gabidullina, Nina Lauterbach, Nandor Varga, Efi Melista: Novel HLA Alleles Based on Polymorphism Outside the Key Exons as a Result of Full Length NGS: What Now?
2018
Libor Kolesár, Efi Melista, Nora Nagy, Peter Meintjes: Conquering the EFI NGS Standards with Holotype HLA and HLA Twin
2017
Efi Melista, Kim McGowan, Doreen Sese, Sharon Adams, Deborah Chen, Tünde Vágó, Eric McCloskey, Zach Smith, Shilpa Parakh, Peter Meintjes: Multi-center Study for Automating Holotype HLA on a Biomek 4000
Ellia Gomes, Efi Melista, Krisztina Rigó, Libor Kolesár, Milena Vrana, Peter Meintjes: NGS Superpowers II: New Capabilities for Challenging Samples
Rachel Breeding, Efi Melista, Xin Wang, John May, Peter Meintjes: Automating Holotype HLA on the Agilent BRAVO NGS Workstation Liquid Handler & Validation for Routine HLA Genotyping
Libor Kolesár, Efi Melista, Krisztina Rigó, Panna Vass, Elena Longhi, Beatrice Bardy, Xavier Lafarge, Peter Meintjes: Superpowers of NGS: Old Challenges Made Easy
Yanping Huang, Matt Galbraith, Deborah Ferriola, Dimitri Monos: High-throughput Automation for NGS-based HLA Typing
2016
Efi Melista, Tina Yu, Tünde Vágó, Willy Hsu, Peter Meintjes, Tim Hague: Automating Holotype HLA on TBG's DX-A™ Robot
Nóra Nagy, Efi Melista, Krisztina Rigó, Peter Meintjes, Tim Hague: The Economics of NGS: A Cost Comparison of NGS Implementations with Legacy Technologies
Efi Melista, Krisztina Rigó, Szilveszter Juhos, Peter Meintjes, Tim Hague: Holotype HLA Early Access Program Results: An “Uncontrolled” Study
2015
Efi Melista, Krisztina Rigó, Ágnes Pásztor, Mette Christiansen, Francesca Eleonora Bertinetto, Peter Meintjes, Tim Hague: Towards a New Gold Standard – NGS Corrections to Sanger SBT Genotyping Results
György Horváth, Krisztina Rigó, Tim Hague, Szilveszter Juhos: Whole-gene Next-generation Sequencing of HLA Genes Reveals Hidden Diversity of Intronic Regions
Tünde Vágó, Péter Tóth, Tim Hague, Szilveszter Juhos: Diversity of MHC Genes in the 1000 Genomes Dataset
2014
Szilveszter Juhos, Krisztina Rigó, György Horváth, Tim Hague: Meta Analysis of Sequence-based HLA Typing Approaches
György Horváth, Krisztina Rigó, Tim Hague, Attila Bérces, Szilveszter Juhos: High Accuracy and High Precision HLA Typing Using Illumina Reads: Typing Algorithm and Perspectives on Novel Allele Discovery
Krisztina Rigó, György Horváth, Szilveszter Juhos, Sabine Canivet, Philippe Pellet, Abdelali Boudifa, Veronique Bertrand, Ioannis Theodorou: A Case Study for HLA Typing in Clinics: Reproducibility and Flowspace Alignment of NGS Reads
Szilveszter Juhos, Krisztina Rigó, Pierre-Antoine Gourraud, György Horváth: MHC and the 1000 Genomes: Genotyping from Exome Data
2013
Attila Tordai, Dora Inotai, Endre Major, Attila Bérces, Szilveszter Juhos, Tim Hague: Comparing HLA Types of Targeted Amplicon Samples by Analyzing Sanger and Next Generation Sequencing Data
Endre Major, Krisztina Rigó, Attila Bérces, Szilveszter Juhos: Next-Generation Sequencing and HLA-typing: Method Validation Using 1000 Genomes Public Samples
Endre Major, Krisztina Rigó, Attila Bérces, Szilveszter Juhos, Pierre-Antoine Gourraud, Tim Hague: Thousand Genomes and HLA Typing by NGS: Hidden Treasures in Public Short Read Data
Jamie L. Duke, Ariella Sasson, Kate Mackiewicz, Curt Lind, Endre Major, Tim Hague, Attila Bérces, Dimitri Monos: Deriving HLA Typing from Whole MHC Next-generation Sequencing Data
Fumiko Yamamoto, Kalyan Mallempati, Carolyn Bialozynski, Joel Shi, Endre Major, Tim Hague, David Dinauer, Dolly B. Tyan, Marcelo Fernandez-Vina, Matthew W. Anderson: High-Throughput Shotgun Sequencing of the HLA-DQA1 Gene Using Next-generation Sequencing
J. Ryan A. Pena, Attila Bérces, Heather Kent, Endre Major, Tim Hague, Susan L. Saidman: High-Resolution Typing by Next-generation Sequencing in a Clinical HLA Laboratory
Curt Lind, Jamie Duke, Deborah Ferriola, Katarzyna Mackiewicz, Anna Papazoglou, Steven Heron, Dimitri Monos: Next Generation HLA Sequencing on the Illumina MiSeq
2012
E. Major, T. Hague, T. Nagy, K. Rigó, Sz. Juhos, A. Bérces: HLA Typing from Next Generation Sequencing Data