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Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases
Human genome variation may cause differences in traits and disease risks. Disease-causal/susceptible genes and variants for both common and rare diseases can be detected by comprehensive whole-genome analyses, such as whole-genome sequencing (WGS), using next-generation sequencing (NGS) technology a...
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| Udgivet i: | Proc Jpn Acad Ser B Phys Biol Sci |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The Japan Academy
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5743846/ https://ncbi.nlm.nih.gov/pubmed/29129848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2183/pjab.93.042 |
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