🤔 Which biomedical literature resources can help you to explore novel or known genomic variants from the genomics/omics data? 🧬🧬
- LitVar 2.0: https://www.ncbi.nlm.nih.gov/research/litvar2
- Semantic search engine connecting genomic variants in PubMed and PMC.
- https://pubmed.ncbi.nlm.nih.gov/37268776/
- Pubtator 3.0: https://www.ncbi.nlm.nih.gov/research/pubtator3/
- AI-powered semantic and relation search for proteins, variants, diseases and chemicals. Also, integrated into LitVar.
- https://pubmed.ncbi.nlm.nih.gov/38572754/
- enGenome VarChat: https://varchat.engenome.com
- Generative AI assistant for summarizing literature on genomic variants.
- https://pubmed.ncbi.nlm.nih.gov/38579245/
- VarSome: https://varsome.com
- Comprehensive human genomic variant search engine, aggregating data from >140 sources.
- https://pubmed.ncbi.nlm.nih.gov/30376034/
- DISGENET: https://disgenet.com
- Integrative platform linking genes, variants and diseases with Gene-Disease Associations and Variant-Disease associations.
- https://pubmed.ncbi.nlm.nih.gov/31680165/
- Genomenon, Inc Mastermind: https://mastermind.genomenon.com
- Comprehensive genomic literature search and association engine.
- https://pubmed.ncbi.nlm.nih.gov/33281875/