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Titlebook: Research in Computational Molecular Biology; 19th Annual Internat Teresa M. Przytycka Conference proceedings 2015 Springer International Pu

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Exploration of Designability of Proteins Using Graph Features of Contact Maps: Beyond Lattice Modelloop type structures or structures that are loosely packed. Interestingly enough, it can also be seen that these highly designable structures obtained are also common structural motifs found in nature.
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, (Constrained Optimization of Multistate Energies by Tree Search): A Provable and Efficient Algorithan the previous state of the art for provable multistate design (exhaustive search over sequences). . can handle a very wide range of protein flexibility and can enumerate a gap-free list of the best constraint-satisfying sequences in order of objective function value.
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BWM*: A Novel, Provable, Ensemble-Based Dynamic Programming Algorithm for Sparse Approximations of A. in 49 of 67 protein design problems, computing the full ensemble or a close approximation up to two orders of magnitude faster. Performance of BWM. can be predicted cheaply beforehand, allowing selection of the most efficient algorithm for each design problem.
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Efficient Alignment Free Sequence Comparison with Bounded Mismatches, and phylogentic reconstruction. Among the methods based on substring composition, the . (.) measure proposed by Burstein . (RECOMB 2005) admits a straightforward linear time sequence comparison algorithm, while yielding impressive results in multiple applications. An important direction of research
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CRISPR Detection from Short Reads Using Partial Overlap Graphs,tive immune system against phages. Most of the automated tools that detect CRISPR loci rely on assembled genomes. However, many assemblers do not successfully handle repetitive regions. The first tool to work directly on raw sequence data is Crass, which requires that reads are long enough to contai
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HapTree-X: An Integrative Bayesian Framework for Haplotype Reconstruction from Transcriptome and Geotide polymorphism (SNP) site. However, in the case of two heterozygous SNP sites, genotype calling tools cannot determine whether “mutant” alleles from different SNP loci are on the same chromosome or on different homologous chromosomes (i.e. compound heterozygote).
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