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Protocol for a scoping review of multi-omic analysis for rare diseases
INTRODUCTION: The development of next generation sequencing technology has enabled cost-efficient, large scale, multiple ‘omic’ analysis, including epigenomic, genomic, metabolomic, phenomic, proteomic and transcriptomic research. These integrated approaches hold significant promise for rare disease...
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| Vydáno v: | BMJ Open |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6501961/ https://ncbi.nlm.nih.gov/pubmed/31061034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2018-026278 |
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