domains / families / science / long-read-sequencing-agent

long-read-sequencing-agent

separate

AI-powered analysis of long-read sequencing data (PacBio, ONT) for structural variant detection, isoform discovery, epigenetic modifications, and de novo assembly.

When to use

When detecting structural variants (SVs) missed by short-read sequencing.
To characterize full-length transcript isoforms and alternative splicing.
For detecting DNA base modifications (5mC, 6mA) directly from sequencing.
When performing de novo genome assembly for complex regions.
To phase variants and generate fully-resolved haplotypes.

Skill page

Source

Repository	Path
FreedomIntelligence/OpenClaw-Medical-Skills	`skills/long-read-sequencing-agent/SKILL.md`