A scoping review and proposed workflow for multi-omic rare disease research

被引：0
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作者：
Katie Kerr
Helen McAneney
Laura J. Smyth
Caitlin Bailie
Shane McKee
Amy Jayne McKnight
机构：
[1] Queen’s University Belfast,Centre for Public Health
[2] Belfast City Hospital,Regional Genetics Centre
来源：
Orphanet Journal of Rare Diseases | / 15卷
关键词：
Epigenomics; Exomics; Genomics; Methylomics; Multi-omics; Rare disease; Transcriptomics; Whole exome sequencing; Whole genome sequencing;
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