mola links single-nucleotide mismatches to read alignments from all kinds of RNA sequencing data:
- bulk short-read paired-/single-end RNA-seq
- bulk long-read RNA-seq
- single-cell short-read RNA-seq
- single-cell long-read RNA-seq
then implement probabilistic modeling for:
- classification of sequencing errors, RNA editing and germline SNPs
- haplotype phasing
- somatic mutation detection
Install from source for now:
git clone git@github.com:chilampoon/mola.git
cd mola
pip install -e .| Application | Data modality | Publication |
|---|---|---|
| A-to-I editing site calling from HyperTRIBE | Bulk short-read RNA-seq | Inherited resilience to clonal hematopoiesis by modifying stem cell RNA regulation (2026) |
Long-form documentation lives at docs/.