CASPER

CASPER is a software tool used in bioinformatics to improve the performance of downstream tasks like genome assembly and mapping by merging forward and reverse reads from paired-end sequencing. This process helps provide longer, more accurate reads to these tasks. However, the tool faces challenges due to the limitations of most paired-end sequencers, where the chances of observing erroneous bases increase as the end of a read is approached. Despite the existence of other methods to solve this problem, their performance remains unsatisfactory. CASPER addresses this issue through a context-aware scheme that quickly and reliably merges overlapping paired-end reads. It performs better than existing state-of-the-art tools in terms of accuracy and robustness. Additionally, it utilizes parallelism to speed up the process of paired-end merging. CASPER is freely available for academic use at its website.

Topic

Sequencing;Sequence analysis;Mapping

Detail

  • Operation: Read mapping

  • Software interface: Command-line interface

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Publications

  • CaSpER identifies and visualizes CNV events by integrative analysis of single-cell or bulk RNA-sequencing data.
  • Serin Harmanci A, et al. CaSpER identifies and visualizes CNV events by integrative analysis of single-cell or bulk RNA-sequencing data. CaSpER identifies and visualizes CNV events by integrative analysis of single-cell or bulk RNA-sequencing data. 2020; 11:89. doi: 10.1038/s41467-019-13779-x
  • https://doi.org/10.1038/s41467-019-13779-x
  • PMID: 31900397
  • PMC: PMC6941987
  • CASPER: context-aware scheme for paired-end reads from high-throughput amplicon sequencing.
  • Kwon S, et al. CASPER: context-aware scheme for paired-end reads from high-throughput amplicon sequencing. CASPER: context-aware scheme for paired-end reads from high-throughput amplicon sequencing. 2014; 15 Suppl 9:S10. doi: 10.1186/1471-2105-15-S9-S10
  • https://doi.org/10.1186/1471-2105-15-S9-S10
  • PMID: 25252785
  • PMC: PMC4168710
  • QUANTIFYING ALTERNATIVE SPLICING FROM PAIRED-END RNA-SEQUENCING DATA.
  • Rossell D, et al. QUANTIFYING ALTERNATIVE SPLICING FROM PAIRED-END RNA-SEQUENCING DATA. QUANTIFYING ALTERNATIVE SPLICING FROM PAIRED-END RNA-SEQUENCING DATA. 2014; 8:309-330. doi: 10.1214/13-aoas687
  • https://doi.org/10.1214/13-aoas687
  • PMID: 24795787
  • PMC: PMC4005600

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