tailfindr: alignment-free poly(A) length measurement for Oxford Nanopore RNA and DNA sequencing

  1. Eivind Valen1,2
  1. 1Computational Biology Unit, Department of Informatics, University of Bergen, 5008 Bergen, Norway
  2. 2Sars International Centre for Marine Molecular Biology, University of Bergen, 5008 Bergen, Norway
  1. Corresponding author: eivind.valen{at}uib.no
  1. 3 These authors contributed equally to this work.

Abstract

Polyadenylation at the 3′-end is a major regulator of messenger RNA and its length is known to affect nuclear export, stability, and translation, among others. Only recently have strategies emerged that allow for genome-wide poly(A) length assessment. These methods identify genes connected to poly(A) tail measurements indirectly by short-read alignment to genetic 3′-ends. Concurrently, Oxford Nanopore Technologies (ONT) established full-length isoform-specific RNA sequencing containing the entire poly(A) tail. However, assessing poly(A) length through base-calling has so far not been possible due to the inability to resolve long homopolymeric stretches in ONT sequencing. Here we present tailfindr, an R package to estimate poly(A) tail length on ONT long-read sequencing data. tailfindr operates on unaligned, base-called data. It measures poly(A) tail length from both native RNA and DNA sequencing, which makes poly(A) tail studies by full-length cDNA approaches possible for the first time. We assess tailfindr’s performance across different poly(A) lengths, demonstrating that tailfindr is a versatile tool providing poly(A) tail estimates across a wide range of sequencing conditions.

Keywords

Footnotes

  • Received March 22, 2019.
  • Accepted June 25, 2019.

This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.

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