Literature DB >> 24006411

Archival bone marrow trephines are suitable for high-throughput mutation analysis using next generation sequencing technology.

Britta Hasemeier, Robert Geffers, Stephan Bartels, Brigitte Schlegelberger, Hans Kreipe, Ulrich Lehmann.   

Abstract

Entities:  

Keywords:  bone marrow trephines; mutation analysis; sequencing technology

Mesh：

Year:  2013        PMID： 24006411      PMCID： PMC3762114          DOI： 10.3324/haematol.2013.091652

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  8 in total

Review 1.  Real-time PCR analysis of DNA and RNA extracted from formalin-fixed and paraffin-embedded biopsies.

Authors:  U Lehmann; H Kreipe
Journal:  Methods       Date:  2001-12       Impact factor: 3.608

2.  The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories.

Authors:  A Kohlmann; H-U Klein; S Weissmann; S Bresolin; T Chaplin; H Cuppens; E Haschke-Becher; B Garicochea; V Grossmann; B Hanczaruk; K Hebestreit; C Gabriel; I Iacobucci; J H Jansen; G te Kronnie; L van de Locht; G Martinelli; K McGowan; M R Schweiger; B Timmermann; P Vandenberghe; B D Young; M Dugas; T Haferlach
Journal:  Leukemia       Date:  2011-06-17       Impact factor: 11.528

Review 3.  Next-generation sequencing - feasibility and practicality in haematology.

Authors:  Alexander Kohlmann; Vera Grossmann; Niroshan Nadarajah; Torsten Haferlach
Journal:  Br J Haematol       Date:  2013-01-07       Impact factor: 6.998

4.  Targeted, high-depth, next-generation sequencing of cancer genes in formalin-fixed, paraffin-embedded and fine-needle aspiration tumor specimens.

Authors:  Andrew G Hadd; Jeff Houghton; Ashish Choudhary; Sachin Sah; Liangjing Chen; Adam C Marko; Tiffany Sanford; Kalyan Buddavarapu; Julie Krosting; Lana Garmire; Dennis Wylie; Rupali Shinde; Sylvie Beaudenon; Erik K Alexander; Elizabeth Mambo; Alex T Adai; Gary J Latham
Journal:  J Mol Diagn       Date:  2013-01-13       Impact factor: 5.568

5.  Aberrant methylation and impaired expression of the p15(INK4b) cell cycle regulatory gene in chronic myelomonocytic leukemia (CMML).

Authors:  M Tessema; F Länger; J Dingemann; A Ganser; H Kreipe; U Lehmann
Journal:  Leukemia       Date:  2003-05       Impact factor: 11.528

6.  Comparison of targeted next-generation sequencing (NGS) and real-time PCR in the detection of EGFR, KRAS, and BRAF mutations on formalin-fixed, paraffin-embedded tumor material of non-small cell lung carcinoma-superiority of NGS.

Authors:  Katja Tuononen; Satu Mäki-Nevala; Virinder Kaur Sarhadi; Aino Wirtanen; Mikko Rönty; Kaisa Salmenkivi; Jenny M Andrews; Aino I Telaranta-Keerie; Sari Hannula; Sonja Lagström; Pekka Ellonen; Aija Knuuttila; Sakari Knuutila
Journal:  Genes Chromosomes Cancer       Date:  2013-01-30       Impact factor: 5.006

Review 7.  Clinical implications of the molecular genetics of chronic lymphocytic leukemia.

Authors:  Robin Foà; Ilaria Del Giudice; Anna Guarini; Davide Rossi; Gianluca Gaidano
Journal:  Haematologica       Date:  2013-05       Impact factor: 9.941

8.  Targeted high throughput sequencing in clinical cancer settings: formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity.

Authors:  Martin Kerick; Melanie Isau; Bernd Timmermann; Holger Sültmann; Ralf Herwig; Sylvia Krobitsch; Georg Schaefer; Irmgard Verdorfer; Georg Bartsch; Helmut Klocker; Hans Lehrach; Michal R Schweiger
Journal:  BMC Med Genomics       Date:  2011-09-29       Impact factor: 3.063
  8 in total
  2 in total

1.  Comprehensive Molecular Profiling of Archival Bone Marrow Trephines Using a Commercially Available Leukemia Panel and Semiconductor-Based Targeted Resequencing.

Authors:  Stephan Bartels; Elisa Schipper; Hans Heinrich Kreipe; Ulrich Lehmann
Journal:  PLoS One       Date:  2015-07-29       Impact factor: 3.240

Review 2.  Routine clinical mutation profiling using next generation sequencing and a customized gene panel improves diagnostic precision in myeloid neoplasms.

Authors:  Stephan Bartels; Elisa Schipper; Britta Hasemeier; Hans Kreipe; Ulrich Lehmann
Journal:  Oncotarget       Date:  2016-05-24
  2 in total

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