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Titlebook: Algorithms in Bioinformatics; 16th International W Martin‘Frith,Christian Nørgaard Storm Pedersen Conference proceedings 2016 Springer Inte

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楼主: Chylomicron
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Die blaue Stunde der InformatikS spectra per sample, each one having to be compared to a large reference database from which artificial spectra are produced. The goal is to map each experimental spectrum to an artificial one, so as to identify the proteins they come from. However, this comparison step is highly time consuming. Th
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https://doi.org/10.1007/978-3-662-42992-1ld-standard reference alignment of its proteins. In benchmark suites of protein reference alignments, the core columns of the reference are those that can be confidently labeled as correct, usually due to all residues in the column being sufficiently close in the spatial superposition of the folded
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https://doi.org/10.1007/3-540-30519-Xnment, but work directly on a sequence similarity graph. We present a model for constructing a median of three genomes in this family-free setting, based on maximizing an objective function that generalizes the classical breakpoint distance by integrating sequence similarity in the score of a gene a
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Aktuelle Entwicklungen auf nationaler Ebene,presenting paralogs. While a gene tree directly leads to a set of orthology and paralogy relations, the converse is not always true. Indeed a relation graph cannot necessarily be inferred from any tree, and even if it is “satisfiable” by a tree, this tree is not necessarily “consistent”, i.e. does n
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Aktuelle Entwicklungen auf nationaler Ebene,ome sequence. We present the open source .-mer counting software . that has been designed for the efficient counting of .-mers for .. Given the technology trend towards long reads of next-generation sequencers, support for large . becomes increasingly important. While existing .-mer counting tools s
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Aktuelle Entwicklungen auf nationaler Ebene,ng-read sequencing technologies, in metagenomic data intra-genome and, more importantly, inter-genome repeats continue to be a significant impediment to effective genome reconstruction. Detecting repeats in metagenomic samples is complicated by characteristic features of these data, primarily uneven
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https://doi.org/10.1007/3-540-30519-Xasses. The inverse problem is the .: Given all prefix and suffix masses, determine the string of amino acids. In biological reality, the given masses are measured in a lab experiment, and measurements by necessity are noisy. The (real, noisy) . therefore has a noisy input: a few of the prefix and su
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