Next-generation sequencing and its application in acute myeloid leukemia and myelodysplastic syndrome / 中国实验血液学杂志
Journal of Experimental Hematology
; (6): 1545-1549, 2011.
Article
em Zh
| WPRIM
| ID: wpr-331036
Biblioteca responsável:
WPRO
ABSTRACT
The next-generation sequencing (NGS), as the most practical and reliable method, has replaced the classical Sanger sequencing to help scientists to discover the genetics secrets of human tumor diseases. With the technique development, the whole genome sequencing will be no longer out of reach. Recently, some scientists used the NGS in the research of hematological malignancies and pushed the progress of the whole genome sequencing in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) actively in order to find out the pathogenesis of some hematological malignancies. The NGS and the application of the whole genome sequencing, the exome sequencing, the transcriptome sequencing in AML and MDS are reviewed in this article.
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Síndromes Mielodisplásicas
/
Sequência de Bases
/
Leucemia Mieloide Aguda
/
Genoma Humano
/
Análise de Sequência
/
Neoplasias Hematológicas
/
Genética
/
Métodos
Limite:
Humans
Idioma:
Zh
Revista:
Journal of Experimental Hematology
Ano de publicação:
2011
Tipo de documento:
Article