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PreprintCC BY-NC-NDbioRxiv

SCAR: Controlled mutations, ancient DNA damage, and fragmentation of fasta and fastq sequences

  1. 1Technical University of Denmark

Abstract

Controlled modification of sequencing data is important for reproducible benchmarking, particularly when evaluating analyses affected by read fragmentation, divergent reference genomes and ancient DNA damage. SCAR introduces controlled mutations, fragmentation and position-specific damage into FASTA and FASTQ data. All features can be used separately or in combination, and empirical fragment-length and mismatch profiles can be supplied to closely reproduce the properties of targeted datasets. Validation analyses showed the successful implementation of the requested sequence changes, and their impact on read mapping and heterozygosity analyses. Availability and Implementation: SCAR is implemented in C++ and the latest code is available at https://github.com/Madshartmann1/SCAR. The version described in this article is archived at Zenodo at https://doi.org/10.5281/zenodo.22789736 , with validation material available at https://doi.org/10.5281/zenodo.21915766.

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BibTeX
@misc{hartmann2026scar,
  title = {{SCAR: Controlled mutations, ancient DNA damage, and fragmentation of fasta and fastq sequences}},
  author = {M. Hartmann and M. V. Westbury},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.24.754018},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.24.754018v1},
  note = {CC BY-NC-ND},
}
RIS
TY  - UNPB
TI  - SCAR: Controlled mutations, ancient DNA damage, and fragmentation of fasta and fastq sequences
AU  - M. Hartmann
AU  - M. V. Westbury
PY  - 2026
DA  - 2026/09/24
PB  - bioRxiv
DO  - 10.64898/2026.09.24.754018
UR  - https://www.biorxiv.org/content/10.64898/2026.09.24.754018v1
AB  - Controlled modification of sequencing data is important for reproducible benchmarking, particularly when evaluating analyses affected by read fragmentation, divergent reference genomes and ancient DNA damage. SCAR introduces controlled mutations, fragmentation and position-specific damage into FASTA and FASTQ data. All features can be used separately or in combination, and empirical fragment-length and mismatch profiles can be supplied to closely reproduce the properties of targeted datasets. Validation analyses showed the successful implementation of the requested sequence changes, and their impact on read mapping and heterozygosity analyses. Availability and Implementation: SCAR is implemented in C++ and the latest code is available at https://github.com/Madshartmann1/SCAR. The version described in this article is archived at Zenodo at https://doi.org/10.5281/zenodo.22789736 , with validation material available at https://doi.org/10.5281/zenodo.21915766.
ER  -