NGSNGS: next-generation simulator for next-generation sequencing data.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 36661298.
- Also identified by DOI 10.1093/bioinformatics/btad041 and PMC identifier 9891242.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
With the rapid expansion of the capabilities of the DNA sequencers throughout the different sequencing generations, the quantity of generated data has likewise increased. This evolution has also led to new bioinformatical methods, for which in silico data have become crucial when verifying the accuracy of a model or the robustness of a genomic analysis pipeline. Here, we present a multithreaded next-generation simulator for next-generation sequencing data (NGSNGS), which simulates reads faster than currently available methods and programs. NGSNGS can simulate reads with platform-specific characteristics based on nucleotide quality score profiles as well as including a post-mortem damage model which is relevant for simulating ancient DNA. The simulated sequences are sampled (with replacement) from a reference DNA genome, which can represent a haploid genome, polyploid assemblies or even population haplotypes and allows the user to simulate known variable sites directly. The program is implemented in a multithreading framework and is factors faster than currently available tools while extending their feature set and possible output formats. The method and associated programs are released as open-source software, code and user manual are available at https://github.com/RAHenriksen/NGSNGS. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Software
- Genome