Motivation: Cancer researchers seeking immunotherapy targets in cancer cells need tools to locate highly expressed proteins unique to cancer cells. Missense mutation and frameshift location reporter (MMuFLR), a Galaxy-based workflow, analyzes next-generation sequencing paired read RNA-seq output to reliably identify small frameshift mutations and missense mutations in highly expressed protein-coding genes. MMuFLR ignores known SNPs, low quality reads and poly-A/T sequences. For each frameshift and missense mutation identified, MMuFLR provides the location and sequence of the amino acid substitutions in the novel protein candidates for direct input into epitope evaluation tools. © The Author 2013.
CITATION STYLE
Rathe, S. K., Johnson, J. E., Silverstein, K. A. T., Erdmann, J. J., Watson, A. L., Popescu, F. E., … Largaespada, D. A. (2013). MMuFLR: Missense mutation and frameshift location reporter. Bioinformatics, 29(18), 2353–2354. https://doi.org/10.1093/bioinformatics/btt385
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