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mola

Multi-modal Observations from Long- and short-read Alignments

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

Installation

Install from source for now:

git clone git@github.com:chilampoon/mola.git
cd mola
pip install -e .

Use Cases

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)

Documentation

Long-form documentation lives at docs/.

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Single nucleotide variation modeling in RNA sequencing data

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