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Titlebook: Hidden Markov Models; Methods and Protocol David R. Westhead,M. S. Vijayabaskar Book 2017 Springer Science+Business Media LLC 2017 protein.

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發(fā)表于 2025-3-25 04:58:46 | 只看該作者
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發(fā)表于 2025-3-25 13:38:45 | 只看該作者
Self-Organizing Hidden Markov Model Map (SOHMMM): Biological Sequence Clustering and Cluster VisualThe Sequence Data Density Display (SDDD) and Sequence Likelihood Projection (SLP) visualizations represent the input symbolical sequences in a lower-dimensional space in such a way that the clusters and relations of data elements are depicted graphically. Both operate in combination/synergy with the
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發(fā)表于 2025-3-25 18:08:00 | 只看該作者
Analyzing Single Molecule FRET Trajectories Using HMM,and such dynamics in recent biology. The single-molecule F?rster resonance energy transfer (smFRET) measurement is one of few methods that enable us to observe structural changes of biomolecules in realtime. Time series data of smFRET, however, typically contains significant fluctuation, making anal
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發(fā)表于 2025-3-25 23:31:01 | 只看該作者
Modelling ChIP-seq Data Using HMMs, chapter, we show how hidden Markov models can be used for the analysis of data generated by ChIP-seq experiments. We show how a hidden Markov model can naturally account for spatial dependencies in the ChIP-seq data, how it can be used in the presence of data from multiple ChIP-seq experiments unde
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發(fā)表于 2025-3-26 01:42:15 | 只看該作者
Hidden Markov Models in Bioinformatics: SNV Inference from Next Generation Sequence,s (HMMs) have wide applications in pattern recognition as well as Bioinformatics such as transcription factor binding sites and cis-regulatory modules detection. An application of HMM is introduced in this chapter with the in-deep developing of NGS. Single nucleotide variants (SNVs) inferred from NG
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發(fā)表于 2025-3-26 05:34:58 | 只看該作者
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發(fā)表于 2025-3-26 09:14:18 | 只看該作者
Hidden Markov Models in Population Genomics, the genome, sequenced in dozens of individuals, to collections of complete genomes, virtually comprising all available loci. Initially sequenced in a few individuals, such genomic data sets are now reaching and even exceeding the size of traditional data sets in the number of haplotypes sequenced.
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