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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
Protein coding genes constitute only approximately 1% of the human genome but harbor 85% of the mutations with large effects on disease-related traits. Therefore, efficient strategies for selectively sequencing complete coding regions (i.e., “whole exome”) have the potential to contribute to the und...
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| Hlavní autoři: | , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2768590/ https://ncbi.nlm.nih.gov/pubmed/19861545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0910672106 |
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