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ASHI 2016, St. Louis USA
P082, HLA Disease association assignment by multiplexed NGS assay, Westerink N. et al.
P080, The Robust NGSgo workflow for high-resolution HLA typings also fully compatible with the Ion S5 platform, Bouwmans E.E., Rasmussen T.B., et al.
EFI 2016, Kos Greece
P107, Quality criteria guidelines for NGS-based HLA typing using NGSgo® workflow that is compatible with Illumina MiSeq, Van de Pasch L.A.L. et al.
P89, Optimized GSSP set v3.0 combining SBTexcellerator and AlleleSEQR primers for the highest resolution power possible, Rozemuller E.H. et al.
P230, A whole gene NGSgo amplification strategy enabling HLA-DQB1 allelic typing resolution, Bouwmans E.E. et al.
APHIA 2015, Bangkok Thailand
NGS unveiling immunogenic irregularities that were previously conceiled, Van de Pash L.A.L, Dalva K. et al.
ASHI 2015, Savannah USA
P069, High-throughput and cost-effective NGS strategy for intermediate-resolution HLA typing, Rebel C. et al.
P072 High-resolution HLA typings obtained for high-throughput NGS using the Illumina MiSeq platform, Bacelar M. et al.
EFI 2015, Geneva Switzerland
P133, Rapid microchimerism analysis using multiplexed reagents, novel software and quantitative PCR, Luiken B. et al.
P126, A novel and robust NGSgo workflow for high-resolution HLA typings on the IonTorrent PGM platform, Van Aard R. et al.
P54, Hybrid reads, a quality value for HLA amplification: measured with NGSengine®, Kooster R. et al.
P127, A multi-center case study toevaluate the NGSgo high throughput workflow for high-resolution HLA typings, Van de Pasch L.A.L. et al.
ASHI 2014, Denver USA
P164, Hybrid reads, a quality value for HLA amplification: measured with NGSengine®, Kooter R. et al.
P2014, Platform-independent software and reagents for qPCR-based microchimerism analysis, Adema J. et al.
Pac2014, Evaluation of multiplexing strategies for HLA genotyping using PacBio® Sequencing technology, Renade S. et al.
P03, A full NGS workflow for reaching the ultimate HLA typing resolution, Adema J et al.
P01, Improved SBTengine® batch analysis module, Rozemuller E.H. et al.
EFI 2014, Stockholm Sweden
P14016, An update on NGSengine®: the ultimate tool for NGS HLA typing, Kooster R. et al.
P14017, Improved SBTengine® batch analysis module, Rozemuller E.H. et al.
P156, Ultimate HLA typing resolution by optimized NGS workflow, Adema J. et al.
Multiplexed Reagents and Novel Software for qPCR-Based Microchimerism Analysis
ASHI 2013, Chicago USA
P01, NGSengine®:the ultimate tool for NGS HLA-typing, Kooster R. et al.
P02, NGS early access program: findings in a multicentre evaluation, Penning M.T. et al.
P04, Novel Software and Reagents for qPCR-Based Transplant Monitoring, Roovers D. et al.
P05, Labflow Lite: A digital lab assistent for an efficient SBT laboratory workflow, De Jager E. et al.
EFI 2013, Maastricht the Netherlands
P118, NGS early access program: findings in a multicentre evaluation, Penning M.T. et al.
P111, A multi-centre case study to evaluate HLA typing resolution using a novel SBTessenz® assay, Adema J. et al.
P153, NGSengine® the ultimate tool for NGS HLA-typing, Kooter R. et al.
NBIC 2013, Lunteren the Netherlands
P01, NGSengine®: the solution for allele identification in highly polymorphic MHC sequences, Kooter R. et al.
ASHI 2012, Puerto Rico
P47, High-throughput sequencing-based HLA-typing, Adema J. et al.
P117, NGSengine®: the ultimate tool for NGS HLA-typing, Rozemuller E.H. et al.
EFI 2012, Liverpool UK
P3, Improved genotype ambiguity resolution by 2nd generation GSSP’S, Westerink N. et al.
P356, HLA-B*57:01 real-time PCR & Pyrosequencing, Penning M.T. et al.
P343, Robust PCR assay for the detection DQ2 and DQ8 for the diagnosis of Celiac Disease, Penning M.T. et al.
P76, HT Sequencing-Based HLA-Typing of HLA DQB1, Adema J. et al.
ASHI 2011, New Orleans USA
P162, SBTengine®,The Ultimate Solution For High Resolution HLA typing, Rozemuller E.H. et al.
P163, High Resolution HLA Typing For Companion Diagnostics Using Pyrosequencing, Penning M.T. et al.
P164, New Robust HLA-B*27 Detection Assay Based on Real-Time PCR, Penning M.T. et al.