Autor: |
Mertes F; Max Planck Institute for Molecular Genetics, Berlin, Germany. mertes@molgen.mpg.de, Elsharawy A, Sauer S, van Helvoort JM, van der Zaag PJ, Franke A, Nilsson M, Lehrach H, Brookes AJ |
Jazyk: |
angličtina |
Zdroj: |
Briefings in functional genomics [Brief Funct Genomics] 2011 Nov; Vol. 10 (6), pp. 374-86. Date of Electronic Publication: 2011 Nov 26. |
DOI: |
10.1093/bfgp/elr033 |
Abstrakt: |
In this review, we discuss the latest targeted enrichment methods and aspects of their utilization along with second-generation sequencing for complex genome analysis. In doing so, we provide an overview of issues involved in detecting genetic variation, for which targeted enrichment has become a powerful tool. We explain how targeted enrichment for next-generation sequencing has made great progress in terms of methodology, ease of use and applicability, but emphasize the remaining challenges such as the lack of even coverage across targeted regions. Costs are also considered versus the alternative of whole-genome sequencing which is becoming ever more affordable. We conclude that targeted enrichment is likely to be the most economical option for many years to come in a range of settings. |
Databáze: |
MEDLINE |
Externí odkaz: |
|