12,984 research outputs found
RNA secondary structure prediction from multi-aligned sequences
It has been well accepted that the RNA secondary structures of most
functional non-coding RNAs (ncRNAs) are closely related to their functions and
are conserved during evolution. Hence, prediction of conserved secondary
structures from evolutionarily related sequences is one important task in RNA
bioinformatics; the methods are useful not only to further functional analyses
of ncRNAs but also to improve the accuracy of secondary structure predictions
and to find novel functional RNAs from the genome. In this review, I focus on
common secondary structure prediction from a given aligned RNA sequence, in
which one secondary structure whose length is equal to that of the input
alignment is predicted. I systematically review and classify existing tools and
algorithms for the problem, by utilizing the information employed in the tools
and by adopting a unified viewpoint based on maximum expected gain (MEG)
estimators. I believe that this classification will allow a deeper
understanding of each tool and provide users with useful information for
selecting tools for common secondary structure predictions.Comment: A preprint of an invited review manuscript that will be published in
a chapter of the book `Methods in Molecular Biology'. Note that this version
of the manuscript may differ from the published versio
Parametric inference of recombination in HIV genomes
Recombination is an important event in the evolution of HIV. It affects the
global spread of the pandemic as well as evolutionary escape from host immune
response and from drug therapy within single patients. Comprehensive
computational methods are needed for detecting recombinant sequences in large
databases, and for inferring the parental sequences.
We present a hidden Markov model to annotate a query sequence as a
recombinant of a given set of aligned sequences. Parametric inference is used
to determine all optimal annotations for all parameters of the model. We show
that the inferred annotations recover most features of established hand-curated
annotations. Thus, parametric analysis of the hidden Markov model is feasible
for HIV full-length genomes, and it improves the detection and annotation of
recombinant forms.
All computational results, reference alignments, and C++ source code are
available at http://bio.math.berkeley.edu/recombination/.Comment: 20 pages, 5 figure
Spectral Sequence Motif Discovery
Sequence discovery tools play a central role in several fields of
computational biology. In the framework of Transcription Factor binding
studies, motif finding algorithms of increasingly high performance are required
to process the big datasets produced by new high-throughput sequencing
technologies. Most existing algorithms are computationally demanding and often
cannot support the large size of new experimental data. We present a new motif
discovery algorithm that is built on a recent machine learning technique,
referred to as Method of Moments. Based on spectral decompositions, this method
is robust under model misspecification and is not prone to locally optimal
solutions. We obtain an algorithm that is extremely fast and designed for the
analysis of big sequencing data. In a few minutes, we can process datasets of
hundreds of thousand sequences and extract motif profiles that match those
computed by various state-of-the-art algorithms.Comment: 20 pages, 3 figures, 1 tabl
Learning Phrase Representations using RNN Encoder-Decoder for Statistical Machine Translation
In this paper, we propose a novel neural network model called RNN
Encoder-Decoder that consists of two recurrent neural networks (RNN). One RNN
encodes a sequence of symbols into a fixed-length vector representation, and
the other decodes the representation into another sequence of symbols. The
encoder and decoder of the proposed model are jointly trained to maximize the
conditional probability of a target sequence given a source sequence. The
performance of a statistical machine translation system is empirically found to
improve by using the conditional probabilities of phrase pairs computed by the
RNN Encoder-Decoder as an additional feature in the existing log-linear model.
Qualitatively, we show that the proposed model learns a semantically and
syntactically meaningful representation of linguistic phrases.Comment: EMNLP 201
A Factor Graph Approach to Automated Design of Bayesian Signal Processing Algorithms
The benefits of automating design cycles for Bayesian inference-based
algorithms are becoming increasingly recognized by the machine learning
community. As a result, interest in probabilistic programming frameworks has
much increased over the past few years. This paper explores a specific
probabilistic programming paradigm, namely message passing in Forney-style
factor graphs (FFGs), in the context of automated design of efficient Bayesian
signal processing algorithms. To this end, we developed "ForneyLab"
(https://github.com/biaslab/ForneyLab.jl) as a Julia toolbox for message
passing-based inference in FFGs. We show by example how ForneyLab enables
automatic derivation of Bayesian signal processing algorithms, including
algorithms for parameter estimation and model comparison. Crucially, due to the
modular makeup of the FFG framework, both the model specification and inference
methods are readily extensible in ForneyLab. In order to test this framework,
we compared variational message passing as implemented by ForneyLab with
automatic differentiation variational inference (ADVI) and Monte Carlo methods
as implemented by state-of-the-art tools "Edward" and "Stan". In terms of
performance, extensibility and stability issues, ForneyLab appears to enjoy an
edge relative to its competitors for automated inference in state-space models.Comment: Accepted for publication in the International Journal of Approximate
Reasonin
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