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Ryan E. Mills

Publications and source records attributed to Ryan E. Mills.

2 recordsLinked to original sources

SPECtre: a spectral coherence-based classifier of actively translated transcripts from ribosome profiling sequence data

SummaryActive protein translation can be assessed and measured using ribosome profiling sequencing strategies. Existing analytical approaches applied to this technology make use of sequence fragment length or frame occupancy to differentiate between active translation and background noise, however they do not consider additional characteristics inherent to the technology which limits their overall accuracy. Here, we present an analytical tool that models the overall tri-nucleotide periodicity of ribosomal occupancy using a classifier based on spectral coherence. Our software, SPECtre, examines the relationship of normalized ribosome profiling read coverage over a rolling series of windows along a transcript against an idealized reference signal. A comparison of SPECtre against current methods on existing and new data shows a marked improvement in accuracy for detecting active translation and exhibits overall high sensitivity at a low false discovery rate.\n\nAvailability and ImplementationSPECtre source code is available for download at https://github.com/mills-lab/spectre.\n\nContact: remills@med.umich.edu

Bioinformatics

Resolving Complex Structural Genomic Rearrangements using a Randomized Approach

Complex chromosomal rearrangements consist of structural genomic alterations involving multiple instances of deletions, duplications, inversions, or translocations that co-occur either on the same chromosome or represent different overlapping events on homologous chromosomes. We present SVelter, an algorithm that first identifies regions of the genome suspected to harbor a complex event and then iteratively rearranges the local genome structure, in a randomized fashion, with each structure scored against characteristics of the observed sequencing data. We show that SVelter is able to accurately reconstruct these regions when compared to well-characterized genomes that have been deep sequenced with both short and long read technologies.

Bioinformatics