Impulse Biosample lets users fund the analysis of a selected biosample, incentivizing scientists to study its genetic variants. Donations directly contribute to covering the research costs.
Your contribution directly supports:
Certified bioinformatics analysts
Accredited sequencing laboratories
Secure genetic variant analysis
Transaction Details:
Contribution Amount: 0.0 ATP
Platform Fee: 10%
Net Research Contribution: 0.0 ATP
By contributing ATP tokens, you're:
Accelerating precision medicine research
Supporting validated scientific analysis
Maintaining data sovereignty through BioNFTs™ technology
All transactions comply with regulatory standards for genomic data handling.
By contributing to this biosample, you are helping drive research forward and reward
scientists for analyzing genetic variants.
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10% commission to impulse. Make sure you have enough ATPS
VARIANT AI DESCRIPTOR
Create Researcher Profile
Create your researcher profile to access Claude Code for Bioinformatics. You'll have limited access to curated variants only.
Privacy Notice: Your profile will be used for access tracking and attribution only. Limited to curated variants.
Variant Curation Pipeline Explained
Full Dataset
41230711101565.deepvariant.csv
Total Variants:~4,523,891
Protein-Coding:~23,456
Clinically Relevant:~127
Curated Top 3
Selected based on multiple criteria:
Phenotype Match Score > 0.65
ClinVar: Uncertain Significance
Novel/Rare (gnomAD AF < 0.001)
CADD Score > 20
Curation Pipeline Steps
[DeepVariant CSV] (~4.5M variants)
↓
Filter: Protein-Coding Only
↓
[23,456 variants]
↓
HPO Phenotype Matching
(Match to: Renal Tubular Acidosis)
↓
[127 candidates]
↓
ClinVar + ACMG Criteria
(Clinical significance review)
↓
[15 high-priority]
↓
Expert Curation + Literature
(Manual review by bioinformatician)
↓
[3 TOP CURATED VARIANTS] ✨
Why This Matters
This rigorous curation process reduces 4.5 million variants down to 3 actionable candidates,
focusing researcher attention on variants most likely to explain the patient's phenotype. This is the power of
BioNFT + Claude Code - making genomic data accessible and interpretable.