Leveraging the new with the old: providing a framework for the integration of historic microarray studies with next generation sequencing.
BMC Bioinformatics
; 15 Suppl 11: S3, 2014.
Article
en En
| MEDLINE
| ID: mdl-25350881
ABSTRACT
Next Generation Sequencing (NGS) methods are rapidly providing remarkable advances in our ability to study the molecular profiles of human cancers. However, the scientific discovery offered by NGS also includes challenges concerning the interpretation of large and non-trivial experimental results. This task is potentially further complicated when a multitude of molecular profiling modalities are available, with the goal of a more integrative and comprehensive analysis of the cancer biology.
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Análisis de Secuencia por Matrices de Oligonucleótidos
/
Perfilación de la Expresión Génica
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Secuenciación de Nucleótidos de Alto Rendimiento
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Neoplasias
Límite:
Humans
Idioma:
En
Revista:
BMC Bioinformatics
Asunto de la revista:
INFORMATICA MEDICA
Año:
2014
Tipo del documento:
Article