| HOME | HELP | CONTACT US | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Special Section on Colorectal Cancer |
Queens University, Belfast, Northern Ireland, United Kingdom, and ArraDx Ltd, Craigavon, Northern Ireland, United Kingdom
Key Words. Genomics • Array-based comparative genomic hybridization • Single-nucleotide polymorphism arrays • Microarrays • RNA Later • Formalin-fixed paraffin-embedded
Correspondence: D. Paul Harkin, Ph.D., Chief Executive Officer, ArraDx Ltd, Marty Murphy Building, 19 Seagoe Industrial Estate, Craigavon, Co. Armagh BT63 5QD, Northern Ireland, UK. Telephone: +44 (0) 28 3833 7575; Fax: +44 (0) 28 3839 8676; e-mail: paul.harkin{at}arradx-almac.com
High-throughput genomic technologies have the potential to have a major impact on preclinical and clinical drug development and the selection and stratification of patients in clinical trials. These technologies, which are at varying stages of commercialization, include array-based comparative genomic hybridization, single-nucleotide polymorphism arrays, and (the most mature example) expression-based arrays. One of the rate-limiting steps in the routine clinical application of expression array-based technology is the need for suitable clinical samples. One of the major challenges moving forward, therefore, relates to the ability to use formalin-fixed, paraffin-embeddedderived tissue in expression profiling-based approaches.
This article has been cited by other articles:
![]() |
P. G. Johnston The Colorectal Cancer Coalition: Reflections on the Future Oncologist, October 1, 2006; 11(9): 970 - 972. [Full Text] [PDF] |
||||
| HOME | HELP | CONTACT US | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| THE ONCOLOGIST | STEM CELLS | CME | ALPHAMED PRESS JOURNALS |