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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...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Korea Genome Organization
2012
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| Gaiak: | |
| Sarrera elektronikoa: | 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 |
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