Isoform Discovery in Long-Read Sequencing: Tuning Computational Pipeline
Isoform determination is crucial for understanding the functional diversity of proteins. However, obtaining high-quality sequencing data and optimizing bioinformatics tools for upstream analysis can be challenging. In this study, we present the optimization of a selected software pipeline using the Spike-In RNA Variant (SIRV) standard kit, which contains a diverse set of synthetic isoforms that mimic transcriptome complexity. SIRV data serves as a gold standard, enabling parameter tuning of software tools based on these synthetic reads. We applied the optimized pipeline to long-read sequencing data generated from the same SIRV molecular biology kit to enhance isoform detection capabilities. Our results highlight the importance of parameter optimization and demonstrate the advantages of long-read sequencing in resolving complex isoform structures. This approach offers improved accuracy in isoform identification, contributing to a more comprehensive understanding of protein diversity and function.
Authors
- Elizabeth Tapia (ORCID: https://orcid.org/0000-0002-9363-4824)
- Natalia Iglesias
- Pilar Bulacio
- Ignacio Garcia Labari (ORCID: https://orcid.org/0009-0009-3867-918X)
- Flavio E. Spetale (ORCID: https://orcid.org/0000-0002-0226-8372)
- Sergio Ponce (ORCID: https://orcid.org/0000-0003-2014-2957)
Institutions
- National Technological University (AR)
- Consejo Nacional de Investigaciones Científicas y Técnicas (AR)
- Centro Internacional Franco-Argentino de Ciencias de la Información y de Sistemas (AR)
Publication Details
- Published
- 2024-09-18
- DOI
- https://doi.org/10.1109/argencon62399.2024.10735861
- Primary Topic
- Algorithms and Data Compression
- Type
- article
- Field-Weighted Citation Impact
- 0.00