Cargando…
Clinical Interpretation of Genomic Variations
Novel high-throughput sequencing technologies generate large-scale genomic data and are used extensively for disease mapping of monogenic and/or complex disorders, personalized treatment, and pharmacogenomics. Next-generation sequencing is rapidly becoming routine tool for diagnosis and molecular mo...
Autor principal: | Sayitoğlu, Müge |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111461/ https://www.ncbi.nlm.nih.gov/pubmed/27507302 http://dx.doi.org/10.4274/tjh.2016.0149 |
Ejemplares similares
-
Computational approaches to interpreting genomic sequence variation
por: Ritchie, Graham RS, et al.
Publicado: (2014) -
PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia
por: Küçükcankurt, Fulya, et al.
Publicado: (2020) -
Novel RUNX1 Variation in B-cell Acute Lymphoblastic Leukemia
por: Qipa, Egzona, et al.
Publicado: (2023) -
Using mechanistic models for the clinical interpretation of complex genomic variation
por: Peña-Chilet, María, et al.
Publicado: (2019) -
Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes
por: Petrovski, Slavé, et al.
Publicado: (2013)