Today we launched https://t.co/HxscsoBmHs a variant interpretation knowledge-base server, for rare diseases and cancer. Get variant ACMG/AMP insights and pharmacogenomic details for actionability.
Enjoy browsing Horizon.
#genome#genomics#wholegenome
Strange. Specialized tools are built precisely because general-purpose LLMs fail, this study outcome relies entirely on the specific software the authors chose.
The study shouldn't use a generic title; it should explicitly state: "X, Y LLM outperforms A, B specialized software."
TF4 Gene variants and neurodevelopmental disorders.
Part of GenomeArc's clinical genetics case series.
👉 Registration link in the comments.
📍 Watch (May 25, 2026) the case series on TCF4-related disorders:https://t.co/FgREZoHmVk
#raredisease#TCF4
Amazing! Since its launch one month ago, 50 genomic institutes are using Horizon ACMG/AMP variant classification server with free global access.
Search your rare disease or tumor variant: https://t.co/HxscsoBmHs
#raredisease#cancer#tumor#ACMG#AMP#variant#VUS
PTEN is a notorious pleiotropic gene; viewing both somatic and germline pathogenicity on a single page makes it easy to visualize disease associations across both cancer and rare diseases.
Integrating ACMG and AMP for each variant.
#cancer#somatic#rarediseases#PTEN
To resolve VUS variants, Horizon Variant Knowledgebase provides global open access to additional insights with identical variants.
Search your VUS (SNV, Indel, SVs) to gain more insights:
https://t.co/HxscsoBmHs
#VUS#rarediseases#Genome#Gene
To resolve VUS variants, Horizon Variant Knowledgebase provides global open access to additional insights with identical variants.
Search your VUS (SNV, Indel, SVs) to gain more insights:
https://t.co/HxscsoBmHs
#VUS#rarediseases#Genome#Gene
Search any variant to learn about their ACMG or AMP pathogenicity for #raredisease or #cancer This is free to use, and includes SNV, indels, and SVs, with non-coding annotations as well.
Horizon variant search server: https://t.co/HxscsoBmHs
#rarediseases#cancer#genome#VUS
Search your somatic variants to learn AMP Tier classification, drug insights and from additional tumors:
-AMP Tier classification
-FDA-approved drug insights
-Additional supporting tumor data
🚀 Search Your Somatic Variant: https://t.co/y5dW0oYTKL
#cancer#tumor#somatic
Type your SNV or Structural Variant (SV) to learn pathogenicity, germline or somatic. Interpreting SVs remains a great challenge in clinical #genomics. Excited to share a global variant insight resource (following ACMG and AMP guidelines), search variant: https://t.co/I1ELjjUdfO