esloco: simulation-based estimation of local coverage in long-read DNA sequencing
Abstract
SUMMARY: Long-read DNA sequencing is increasingly applied for whole-genome studies, yet experimental planning often lacks reliable estimates of target region coverage, leading to costly and time-consuming pilot studies and replicates. We present esloco, a Monte Carlo-based simulation framework for estimating local coverage in long-read sequencing experiments, including scenarios with unknown target regions (e.g. viral integration, CRISPR-Cas9) or PCR-free designs (e.g. base modifications). By modeling coverage as a function of sequencing depth and read length distribution, esloco enables informed predictions of local sequencing outcomes. Benchmarking across a 45-gene panel demonstrated close agreement with empirical data, underscoring the framework's reliability. AVAILABILITY AND IMPLEMENTATION: esloco is a Python package available on PyPI (https://pypi.org/project/esloco/), GitHub (https://github.com/aweich/esloco), and Zenodo (https://doi.org/10.5281/zenodo.17776161).
Fields of Study & Subjects
Genomics and Phylogenetic Studies
Genomic variations and chromosomal abnormalities
Single-cell and spatial transcriptomics
Publication details
- Journal / source
- Bioinformatics
- Volume
- 42
- Issue
- 2
- Publication date
- 3 January 2026
- Language
- EN