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Updated: Feb 13, 2026

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
Published on: June 24, 2021
AltHapAlignR: improved accuracy of RNA-seq analyses through the use of alternative haplotypes
Wanseon Lee1, Katharine Plant1, Peter Humburg1
1Wellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Motivation:
Reliance on mapping to a single reference haplotype currently limits accurate estimation of allele or haplotype-specific expression using RNA-sequencing, notably in highly polymorphic regions such as the major histocompatibility complex.
Results:
We present AltHapAlignR, a method incorporating alternate reference haplotypes to generate gene- and haplotype-level estimates of transcript abundance for any genomic region where such information is available. We validate using simulated and experimental data to quantify input allelic ratios for major histocompatibility complex haplotypes, demonstrating significantly improved correlation with ground truth estimates of gene counts compared to standard single reference mapping. We apply AltHapAlignR to RNA-seq data from 462 individuals, showing how significant underestimation of expression of the majority of classical human leukocyte antigen genes using conventional mapping can be corrected using AltHapAlignR to allow more accurate quantification of gene expression for individual alleles and haplotypes.
Availability And Implementation:
Source code freely available at https://github.com/jknightlab/AltHapAlignR.
Supplementary Information:
Supplementary data are available at Bioinformatics online.
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