bioRxivGenomicsPreprint
Bramble: projection of spliced genomic alignments into transcriptomic space for improved transcript quantification
Zoe RudnickiD, Ales VarabyouiD, Rob PatroiD, Mihaela PerteaiD
Abstract
Accurate transcript abundance estimation is central to many transcriptomic studies. Many current quantification methods rely on reads mapped directly to the transcriptome, but transcriptome alignment can misassign reads from unannotated transcripts to annotated isoforms, leading to biased abundance estimates. We introduce Bramble, a method that projects spliced genomic alignments into transcriptomic coordinates to produce alignments compatible with downstream transcript quantification tools. Across simulated short- and long-read RNA-seq datasets and multiple levels of reference annotation completeness, incorporating Bramble into quantification pipelines consistently improved accuracy and reduced error. These results suggest that genome-derived transcriptomic alignments can improve transcript quantification by preserving compatible alignments to annotated transcripts while filtering alignments likely originating from unannotated transcripts.
- assay: bulk RNA-seq
- research focus: differential expression
- research focus: variant calling
- research focus: gene regulatory network inference
- approach: experimental assay
- Citations
- 0
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