tappAS: a comprehensive computational framework for the analysis of the functional impact of differential splicing

Lorena de la Fuente(Hospital Universitario Fundación Jiménez Díaz), Ángeles Arzalluz-Luque(Universitat Politècnica de València), Manuel Tardáguila(Wellcome Sanger Institute), Héctor del Risco(University of Florida), Cristina Martí(Centro de Investigacion Principe Felipe), Sonia Tarazona(Universitat Politècnica de València), Pedro Salguero(Centro de Investigacion Principe Felipe), Raymond Scott(University of Florida), Alberto Lerma-Aguilera(Centro de Investigacion Principe Felipe), Ana Alastrue‐Agudo(Wellcome Sanger Institute), Pablo Bonilla(Wellcome Sanger Institute), Jeremy R. B. Newman(University of Florida), Shunichi Kosugi(University of Florida), Lauren M. McIntyre(University of Florida), Victoria Moreno‐Manzano(Centro de Investigacion Principe Felipe), Ana Conesa(University of Florida)
Genome biology
May 18, 2020
Cited by 71Open Access
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Abstract

Recent advances in long-read sequencing solve inaccuracies in alternative transcript identification of full-length transcripts in short-read RNA-Seq data, which encourages the development of methods for isoform-centered functional analysis. Here, we present tappAS, the first framework to enable a comprehensive Functional Iso-Transcriptomics (FIT) analysis, which is effective at revealing the functional impact of context-specific post-transcriptional regulation. tappAS uses isoform-resolved annotation of coding and non-coding functional domains, motifs, and sites, in combination with novel analysis methods to interrogate different aspects of the functional readout of transcript variants and isoform regulation. tappAS software and documentation are available at https://app.tappas.org.


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