M Dafil

Opinions are my own! 🇨🇦🇧🇩

[M Dafil @dafil]

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

[GenomeArc @genomearc]

Watch all Horizon case series: https://t.co/lTJzPtwFnz

[GenomeArc @genomearc]

Struggling with tricky variants in rare neurodevelopmental disorders?

We unpacked 3 real cases in Horizon Series:

🧬 TCF4 – broader phenotypes
🧬KCNH1 - G6PD focal epilepsy
🧬KMT2D – Kabuki syndrome

Long-read genomics delivering answers.

#raredisease #Genomics #VUS #Gene

[Cristiano Ronaldo @Cristiano]

RIP THE SCRIPT @Nike

#Ad

[Speed⭐️ @ishowspeedsui]

WORLD CUP VIDEO OUT NOW!!!!⚽️

[GenomeArc @genomearc]

Global Access, for everyone, predicting variant effect for rare disease (ACMG) and cancer (AMP).

Type you germline or somatic variant for interpretation:
https://t.co/HxscsoBmHs

#raredisease #cancer #tumor #VUS #longread #genomics #genome #ACMG #AMP #somatic

[GenomeArc @genomearc]

NF1 deletion increases tumor risk. Horizon variant server returns multi-layer insights for geneticists:
🧬pathogenicity,
💊clinical trial drug insight,
🏥 three additional NF1 deletion samples
Search your CNV/SV: https://t.co/HxscsoBmHs

#NF1 #rarediseases #cancer #tumor #CNV

[GenomeArc @genomearc]

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

[GenomeArc @genomearc]

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

[GenomeArc @genomearc]

💡 This snapshot from the Horizon multimodal platform shows:
-Germline ACMG Pathogenicity
-Somatic AMP Tiers
-Pharmacogenomic Insights
-Case Insights
Search your variant, free global access: https://t.co/HxscsoBmHs

[GenomeArc @genomearc]

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

[GenomeArc @genomearc]

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

[GenomeArc @genomearc]

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

[GenomeArc @genomearc]

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

[Mark Carney @MarkJCarney]

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.

[M Dafil @dafil]

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

[M Dafil @dafil]

Unlocking Genomic Variant Insights: Your Free Resource for Rare Disease (Germline) and Cancer (Somatic) Variants https://t.co/piUcZgX7pm

[M Dafil @dafil]

Unlocking Genomic Variant Insights: Your Free Resource for Rare Disease (Germline) and Cancer (Somatic) Variants https://t.co/piUcZgX7pm

[GenomeArc @genomearc]

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

[M Dafil @dafil]

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