Comments (1)
Hi, as of now, we do not have concrete plans for that. However, it is straightforward, as long as you have RNA-seq data that is aligned to the specific genome version that you are interested in.
To run AbSplice on another genome version, you would need to use tissue-specific SpliceMaps from that genome version. We used large RNA-seq cohorts from GTEx to create SpliceMaps, which were available for hg19 (GTEx v7) and hg38 (GTEx v8). If you have data available that is aligned to the T2T CHM13v2.0 (hs1) reference genome you can create SpliceMaps for any tissue and run AbSplice on them. To create SpliceMaps see the example notebook: https://github.com/gagneurlab/splicemap/blob/master/notebooks/example.ipynb
Let me know if you need any further assistance on that.
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Related Issues (16)
- Add AbSplice to environment.yaml
- Bugs in Absplice implementation HOT 18
- Absplice-RNA HOT 3
- Convert EBM model to ONNX to get rid of interpret dependency HOT 3
- can't install, stop at "Solving environment: |" HOT 2
- How to add specific tissues like the retina into the source code HOT 7
- Container Environment problem HOT 2
- How to get CATs data HOT 7
- Splicemap_tissues HOT 3
- License HOT 1
- Can't find cause of the error HOT 2
- SpliceAI running time HOT 5
- Numpy Error appears in Example-Workflow-Execution HOT 6
- Can't get attribute 'EBMPreprocessor' on <module 'interpret.glassbox.ebm.ebm' HOT 2
- Add SpliceMap info to AbSplice output
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