Bmc Medical Genomics

Whole exome sequencing in three families segregating a pediatric case of sarcoidosis

Selecting precise reference normal tissue samples for cancer research using a deep learning approach

Defining housekeeping genes suitable for RNA-seq analysis of the human allograft kidney biopsy tissue

Comparison of DNA methylation profiles associated with spontaneous preterm birth in placenta and cord blood

Hepatic transcriptomic signatures of statin treatment are associated with impaired glucose homeostasis in severely obese patients

Elevated neoantigen levels in tumors with somatic mutations in the HLA-A, HLA-B, HLA-C and B2M genes

Genomics of lipid-laden human hepatocyte cultures enables drug target screening for the treatment of non-alcoholic fatty liver disease

Pathway networks generated from human disease phenome

Min-redundancy and max-relevance multi-view feature selection for predicting ovarian cancer survival using multi-omics data

Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records