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BMCBI
2008
131views more  BMCBI 2008»
14 years 9 months ago
Major copy proportion analysis of tumor samples using SNP arrays
Background: Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the human genome and are useful as genomic markers. Oligonucleotide SNP microarrays ha...
Cheng Li, Rameen Beroukhim, Barbara A. Weir, Wendy...
DAS
2008
Springer
14 years 11 months ago
Writer-Dependent Recognition of Handwritten Whiteboard Notes in Smart Meeting Room Environments
In this paper we present a writer-dependent handwriting recognition system based on hidden Markov models (HMMs). This system, which has been developed in the context of research o...
Marcus Liwicki, Andreas Schlapbach, Horst Bunke
ISER
1999
Springer
112views Robotics» more  ISER 1999»
15 years 1 months ago
Models for Automated Earthmoving
Abstract: We present a composite forward model of the mechanics of an excavator backhoe digging in soil. This model is used to predict the trajectories developed by a closed-loop f...
Howard Cannon, Sanjiv Singh
86
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WABI
2007
Springer
110views Bioinformatics» more  WABI 2007»
15 years 3 months ago
Haplotype Inference Via Hierarchical Genotype Parsing
The within-species genetic variation due to recombinations leads to a mosaic-like structure of DNA. This structure can be modeled, e.g. by parsing sample sequences of current DNA w...
Pasi Rastas, Esko Ukkonen
CORR
2010
Springer
123views Education» more  CORR 2010»
14 years 8 months ago
Feature Construction for Relational Sequence Learning
Abstract. We tackle the problem of multi-class relational sequence learning using relevant patterns discovered from a set of labelled sequences. To deal with this problem, firstly...
Nicola Di Mauro, Teresa Maria Altomare Basile, Ste...