Skip to content

Feature Request/Collaboration: Support for Long-Read (Nanopore) Data Validation #2

Description

@husamia

Background

I am a senior sequencing engineer at Cincinnati Children's Hospital Medical Center. We are currently working with several transgenic mouse models involving CRISPR-mediated editing. We have generated Oxford Nanopore long-read data and successfully identified several insertion sites that we are looking to characterize further.

Proposal

I recently read your preprint, "ISdetector: precise mapping of insertion sequences and associated structural variations from short-read sequencing data," and noticed that long-read integration is listed as a future direction for the tool.

I am interested in validating ISdetector on our long-read datasets. Our data could serve as a practical benchmark for the tool’s expansion into long-read structural variant (SV) and insertion sequence (IS) detection, particularly in complex eukaryotic genomes like the mouse.

Contact for Collaboration

I would love to discuss a potential collaboration or act as an early tester when you begin implementing the long-read feature.

Please reach out to me at: ammar.husami at cchmc.org

Congratulations on the release of the tool!

Best regards,
Ammar

Metadata

Metadata

Assignees

No one assigned

    Labels

    No labels
    No labels

    Projects

    No projects

    Milestone

    No milestone

    Relationships

    None yet

    Development

    No branches or pull requests

    Issue actions