High-depth African genomes inform human migration and health.
PMID:33116287
Highlighting Human Enzymes Active in Different Metabolic Pathways and Diseases: The Case Study of EC 1.2.3.1 and EC 2.3.1.9.
PMID:32751059
Precise breakpoint detection in a patient with 9p- syndrome.
PMID:32532883
Human gene and disease associations for clinical-genomics and precision medicine research.
PMID:32508008
TS-GOEA: a web tool for tissue-specific gene set enrichment analysis based on gene ontology.
PMID:31760951
NPInter v4.0: an integrated database of ncRNA interactions.
PMID:31670377
VarSite: Disease variants and protein structure.
PMID:31606900
Debutant iOS app and gene-disease complexities in clinical genomics and precision medicine.
PMID:31586224
CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases.
PMID:31322791
PhenPath: a tool for characterizing biological functions underlying different phenotypes.
PMID:31307376
Active repurposing of drug candidates for melanoma based on GWAS, PheWAS and a wide range of omics data.
PMID:31221082
Protein-Protein Interaction Network Analysis Reveals Several Diseases Highly Associated with Polycystic Ovarian Syndrome.
PMID:31216618
PanglaoDB: a web server for exploration of mouse and human single-cell RNA sequencing data.
PMID:30951143
Functional and Structural Features of Disease-Related Protein Variants.
PMID:30934684
GM604 regulates developmental neurogenesis pathways and the expression of genes associated with amyotrophic lateral sclerosis.
PMID:30524706