Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

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Publikationen

Suchbegriffe: HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING - METHODS , . Treffer: 17

2018

Zhong, Q; Wagner, U; Kurt, H; Molinari, F; Cathomas, G; Komminoth, P; Barman-Aksözen, J; Schneider-Yin, X; Rey, JP; Vassella, E; Rogel, U; Diebold, J; McKee, T; Jochum, W; Kashofer, K; Hofman, P; Zischka, M; Moch, H; Rechsteiner, M; Wild, PJ Multi-laboratory proficiency testing of clinical cancer genomic profiling by next-generation sequencing.
Pathol Res Pract. 2018; 214(7):957-963
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2017

Szurian, K; Kashofer, K; Liegl-Atzwanger, B Role of Next-Generation Sequencing as a Diagnostic Tool for the Evaluation of Bone and Soft-Tissue Tumors.
Pathobiology. 2017; 84(6):323-338 [OPEN ACCESS]
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2016

St John, EP; Simen, BB; Turenchalk, GS; Braverman, MS; Abbate, I; Aerssens, J; Bouchez, O; Gabriel, C; Izopet, J; Meixenberger, K; Di Giallonardo, F; Schlapbach, R; Paredes, R; Sakwa, J; Schmitz-Agheguian, GG; Thielen, A; Victor, M; Metzner, KJ; Däumer, MP; 454 HIV-1 Alpha Study Group A Follow-Up of the Multicenter Collaborative Study on HIV-1 Drug Resistance and Tropism Testing Using 454 Ultra Deep Pyrosequencing.
PLoS One. 2016; 11(1):e0146687-e0146687 [OPEN ACCESS]
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Weerakkody, RA; Vandrovcova, J; Kanonidou, C; Mueller, M; Gampawar, P; Ibrahim, Y; Norsworthy, P; Biggs, J; Abdullah, A; Ross, D; Black, HA; Ferguson, D; Cheshire, NJ; Kazkaz, H; Grahame, R; Ghali, N; Vandersteen, A; Pope, FM; Aitman, TJ Targeted next-generation sequencing makes new molecular diagnoses and expands genotype-phenotype relationship in Ehlers-Danlos syndrome.
Genet Med. 2016; 18(11):1119-1127
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2015

Belic, J; Koch, M; Ulz, P; Auer, M; Gerhalter, T; Mohan, S; Fischereder, K; Petru, E; Bauernhofer, T; Geigl, JB; Speicher, MR; Heitzer, E Rapid Identification of Plasma DNA Samples with Increased ctDNA Levels by a Modified FAST-SeqS Approach.
Clin Chem. 2015; 61(6):838-849 [OPEN ACCESS]
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Görzer, I; Trajanoski, S; Popow-Kraupp, T; Puchhammer-Stöckl, E Analysis of human cytomegalovirus strain populations in urine samples of newborns by ultra deep sequencing.
J Clin Virol. 2015; 73(18):101-104
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2014

Gabriel, C; Fürst, D; Faé, I; Wenda, S; Zollikofer, C; Mytilineos, J; Fischer, GF HLA typing by next-generation sequencing - getting closer to reality.
Tissue Antigens. 2014; 83(2): 65-75.
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Kastner, R; Zopf, A; Preuner, S; Pröll, J; Niklas, N; Foskett, P; Valent, P; Lion, T; Gabriel, C Rapid identification of compound mutations in patients with Philadelphia-positive leukaemias by long-range next generation sequencing.
Eur J Cancer. 2014; 50(4): 793-800. [OPEN ACCESS]
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Preuner, S; Danzer, M; Pröll, J; Pötschger, U; Lawitschka, A; Gabriel, C; Lion, T High-quality DNA from fingernails for genetic analysis.
J Mol Diagn. 2014; 16(4): 459-466. [OPEN ACCESS]
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Simen, BB; Braverman, MS; Abbate, I; Aerssens, J; Bidet, Y; Bouchez, O; Gabriel, C; Izopet, J; Kessler, HH; Stelzl, E; Di Giallonardo, F; Schlapbach, R; Radonic, A; Paredes, R; Recordon-Pinson, P; Sakwa, J; St John, EP; Schmitz-Agheguian, GG; Metzner, KJ; Däumer, MP; 454 HIV Alphastudy Group An international multicenter study on HIV-1 drug resistance testing by 454 ultra-deep pyrosequencing.
J Virol Methods. 2014; 204(4):31-37
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2013

Heitzer, E; Auer, M; Hoffmann, EM; Pichler, M; Gasch, C; Ulz, P; Lax, S; Waldispuehl-Geigl, J; Mauermann, O; Mohan, S; Pristauz, G; Lackner, C; Höfler, G; Eisner, F; Petru, E; Sill, H; Samonigg, H; Pantel, K; Riethdorf, S; Bauernhofer, T; Geigl, JB; Speicher, MR Establishment of tumor-specific copy number alterations from plasma DNA of patients with cancer.
Int J Cancer. 2013; 133(2):346-356 [OPEN ACCESS]
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Niklas, N; Pröll, J; Danzer, M; Stabentheiner, S; Hofer, K; Gabriel, C Routine performance and errors of 454 HLA exon sequencing in diagnostics.
BMC Bioinformatics. 2013; 14(2):176-176 [OPEN ACCESS]
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Röhr, C; Kerick, M; Fischer, A; Kühn, A; Kashofer, K; Timmermann, B; Daskalaki, A; Meinel, T; Drichel, D; Börno, ST; Nowka, A; Krobitsch, S; McHardy, AC; Kratsch, C; Becker, T; Wunderlich, A; Barmeyer, C; Viertler, C; Zatloukal, K; Wierling, C; Lehrach, H; Schweiger, MR High-throughput miRNA and mRNA sequencing of paired colorectal normal, tumor and metastasis tissues and bioinformatic modeling of miRNA-1 therapeutic applications.
PLoS One. 2013; 8(7):e67461-e67461 [OPEN ACCESS]
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2011

Holcomb, CL; Höglund, B; Anderson, MW; Blake, LA; Böhme, I; Egholm, M; Ferriola, D; Gabriel, C; Gelber, SE; Goodridge, D; Hawbecker, S; Klein, R; Ladner, M; Lind, C; Monos, D; Pando, MJ; Pröll, J; Sayer, DC; Schmitz-Agheguian, G; Simen, BB; Thiele, B; Trachtenberg, EA; Tyan, DB; Wassmuth, R; White, S; Erlich, HA A multi-site study using high-resolution HLA genotyping by next generation sequencing.
Tissue Antigens. 2011; 77(3): 206-217. [OPEN ACCESS]
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Stelzl, E; Pröll, J; Bizon, B; Niklas, N; Danzer, M; Hackl, C; Stabentheiner, S; Gabriel, C; Kessler, HH Human immunodeficiency virus type 1 drug resistance testing: Evaluation of a new ultra-deep sequencing-based protocol and comparison with the TRUGENE HIV-1 Genotyping Kit.
J Virol Methods. 2011; 178(1-2):94-97
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2010

Görzer, I; Guelly, C; Trajanoski, S; Puchhammer-Stöckl, E The impact of PCR-generated recombination on diversity estimation of mixed viral populations by deep sequencing.
J Virol Methods. 2010; 169(1): 248-252.
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Timmermann, B; Kerick, M; Roehr, C; Fischer, A; Isau, M; Boerno, ST; Wunderlich, A; Barmeyer, C; Seemann, P; Koenig, J; Lappe, M; Kuss, AW; Garshasbi, M; Bertram, L; Trappe, K; Werber, M; Herrmann, BG; Zatloukal, K; Lehrach, H; Schweiger, MR Somatic Mutation Profiles of MSI and MSS Colorectal Cancer Identified by Whole Exome Next Generation Sequencing and Bioinformatics Analysis
PLOS ONE. 2010; 5(12): e15661-e15661. [OPEN ACCESS]
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