Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling
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Updated
Feb 26, 2026 - Python
Clair3 - Symphonizing pileup and full-alignment for deep learning-based long-read variant calling
✏️ Genome assembly polishing & SNV detection
VirusWarn-SC2 is a simple Variants of concern aLert system script for SARS-CoV-2.
A mutation-based alert system to prioritize concerning Influenza variants from sequencing data.
Comprehensive Sanger sequence analysis and clinical reporting tool. Identifies SNVs and Indels precisely while keeping your genetic data secure locally.
Optimized Python and C++ implementations of INDELseek, a Perl tool for detecting complex genetic indels in NGS data, with performance improvements, validation, and benchmarking against other variant callers.
Lab module and lectures for variant detection in SARS-CoV-2 using Galaxy
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