IG-28 enables identification and quantification of high-confidence isoforms from large bulk and single-cell full-length cDNA datasets
The technology to sequence full-length transcriptomes from bulk and single-cell samples has rapidly advanced. As a result, full-length cDNA datasets now reach billions of reads in size which is beyond the capability of most established isoform identification tools. Here, we introduce IG-28 which addresses this challenge with its capability to process and analyze large fl-cDNA datasets fast and using minimal computational resources. In contrast to its predecessor Mandalorion, IG-28 is not limited to bulk fl-cDNA but is capable of parsing, processing, and analyzing single-cell fl-cDNA datasets. It does so in a lightweight, flexible manner, integrating seamlessly with established scRNA-seq analysis workflows. We benchmarked IG-28 against a variety of established and new isoform identification tools using several bulk and a complex single-cell fl-cDNA dataset and found that IG-28 consistently outperformed the other tools by identifying high-confidence public isoforms.
Authors
- Christopher Vollmers (ORCID: https://orcid.org/0000-0002-7626-6222)
- Honey Mekonen (ORCID: https://orcid.org/0009-0001-7959-1151)
- Alessandro Calicchio (ORCID: https://orcid.org/0009-0008-7329-2071)
- Amanda O. Li
- Tanvi Herwadkar
Institutions
- University of California, Santa Cruz (US)
Publication Details
- Journal
- bioRxiv (Cold Spring Harbor Laboratory)
- Published
- 2026-10-29
- DOI
- https://doi.org/10.64898/2026.10.23.761370
- Primary Topic
- Genomics and Phylogenetic Studies
- Type
- preprint
Funders
- University of Washington
- Johns Hopkins University
- National Human Genome Research Institute
- National Institute of General Medical Sciences