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Christopher L. Barrett

Publications and source records attributed to Christopher L. Barrett.

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The energy-spectrum of bicompatible sequences

Background: Genotype-phenotype maps provide a meaningful filtration of sequence space and RNA secondary structures are particular such phenotypes. Compatible sequences i.e.~sequences that satisfy the base pairing constraints of a given RNA structure play an important role in the context of neutral networks and inverse folding. Sequences satisfying the constraints of two structures simultaneously are called bicompatible and phenotypic change, induced by erroneously replicating populations of RNA sequences, is closely connected to bicompatibility. Furthermore, bicompatible sequences are relevant for riboswitch sequences, beacons of evolution, realizing two distinct phenotypes. Results: We present a full loop energy model Boltzmann sampler of bicompatible sequences for pairs of structures. The novel dynamic programming algorithm is based on a topological framework encapsulating the relations between loops. We utilize our sequence sampler to study the energy spectra and density of bicompatible sequences, the rankings of the structures and key properties for evolutionary transitions. Conclusion: Our analysis of riboswitch sequences shows that key properties of bicompatible sequences depend on the particular pair of structures. While there always exist bicompatible sequences for random structure pairs, they are less suited to facilitate transitions. We show that native riboswitch sequences exhibit a distinct signature with regards to the ranking of their two phenotypes relative to the minimum free energy, suggesting a new criterion for identifying native sequences and sequences subjected to evolutionary pressure.

q-bio.BM

RNA secondary structures having a compatible sequence of certain nucleotide ratios

Given a random RNA secondary structure, $S$, we study RNA sequences having fixed ratios of nuclotides that are compatible with $S$. We perform this analysis for RNA secondary structures subject to various base pairing rules and minimum arc- and stack-length restrictions. Our main result reads as follows: in the simplex of the nucleotide ratios there exists a convex region in which, in the limit of long sequences, a random structure a.a.s.~has compatible sequence with these ratios and outside of which a.a.s.~a random structure has no such compatible sequence. We localize this region for RNA secondary structures subject to various base pairing rules and minimum arc- and stack-length restrictions. In particular, for {\bf GC}-sequences having a ratio of {\bf G} nucleotides smaller than $1/3$, a random RNA secondary structure without any minimum arc- and stack-length restrictions has a.a.s.~no such compatible sequence. For sequences having a ratio of {\bf G} nucleotides larger than $1/3$, a random RNA secondary structure has a.a.s. such compatible sequences. We discuss our results in the context of various families of RNA structures.

math.CO

TRANSIMS traffic flow characteristics

Knowledge of fundamental traffic flow characteristics of traffic simulation models is an essential requirement when using these models for the planning, design, and operation of transportation systems. In this paper we discuss the following: a description of how features relevant to traffic flow are currently under implementation in the TRANSIMS microsimulation, a proposition for standardized traffic flow tests for traffic simulation models, and the results of these tests for two different versions of the TRANSIMS microsimulation.

adap-org