Загрузка...
Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases
The recent advent of next-generation sequencing technologies has dramatically changed the nature of biomedical research. Human genetics is no exception-it has never been easier to interrogate human patient genomes at the nucleotide level to identify disease-associated variants. To further facilitate...
Сохранить в:
| Главные авторы: | , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Korea Genome Organization
2012
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3543920/ https://ncbi.nlm.nih.gov/pubmed/23346032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5808/GI.2012.10.4.214 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|