We have released SNV/Indel/SV pathogenicity Analysis Software Horizon. With Horizon, you can get germline and somatic variant insight for free. You can start small clinical genomics project yourself right away in our cloud, without a high-spec server.
https://t.co/I1ELjjUdfO
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
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
Doly Begum is ready to build a stronger, more prosperous, and more independent Canadian economy.
Early voting opens today in Scarborough Southwest and Election Day is April 13 — don’t forget to get out and vote.
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
Excited to share our CNV study, 'Horizon: CNV interpretation through rapid automated ACMG-aligned pathogenicity analysis'
#RareDisease#Genetics
Here is the paper: https://t.co/GcWJIVSb0x
You test your CNV/SV pathogenicity, with free access:
https://t.co/HxscsoBmHs
We have released SNV/Indel/SV pathogenicity Analysis Software Horizon. With Horizon, you can get germline and somatic variant insight for free. You can start small clinical genomics project yourself right away in our cloud, without a high-spec server.
https://t.co/I1ELjjUdfO