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En los últimos cuatro años, ha habido un cambio fundamental de la aplicación de sistemas automatizados para el análisis de genoma con secuenciación de ADN de Sanger. Los nuevos métodos de secuenciación hacen referencia a la secuenciación de próxima generación (NGS). Estas nuevas tecnologías constituien diversas estrategias que se basan en una combinación de la preparación de la plantilla, la secuenciación y la imagen, y la alineación del genoma y los métodos de montaje. STAB VIDA ofrece, en su plataforma de NGS, la capacidad de producir un enorme volumen de datos de bajo costo - en algunos casos en más de mil millones de lecturas por instrumentos. En STAB VIDA, los estudios de microarrays para expresión de genes se sustituyen por los métodos basados ​​siguientes, que pueden identificar y cuantificar las transcripciones raras sin conocimiento previo de un gen en particular y puede proporcionar información sobre splicing alternativo y la variación en los genes de secuencia identificada. Tenemos la capacidad de secuenciar todo el genoma de muchos organismos relacionados, que han permitido desarrollar a gran escala los estudios evolutivos y comparativos que eran inimaginables hace pocos años. Podemos proporcionar la nueva secuencia del genoma humano para mejorar la comprensión de cómo las diferencias genéticas afectan a la salud y la enfermedad. La variedad de las características de NGS hace probable que múltiples plataformas van a coexistir en el mercado, con algunas claras ventajas sobre los demás para aplicaciones específicas.

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