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				<project created="2006-10-24 19:02:15" modified="2009-07-21 23:01:36" complexity="1" status="Proposed"/>
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				<properties name="05 - Genotype in detail" type="Logical" documentation="An assay (Variation_assay) is applied to a sample (Molecular_sample) to get a genotype (Assayed_genomic_genotype).  One or more Assayed_genomic_genotype are used to reach a consensus (Consensus_genomic_genotype). The assays commonly use oligo primers to detect allelic variations (Genomic_alleles in Genomic_variation). &#xA;Assay can have reference to possible detectable latent genotype (combination of alleles depending on ploidy). One of these combinations can be detected in single genotype measurement (Assayed_genomic_genotype) done using the specific assay."/>
				<project author="muilu" version="1.0" created="2006-10-25 20:28:55" modified="2009-08-06 11:57:00"/>
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				<project author="muilu" version="1.0" created="2007-09-28 03:31:45" modified="2009-07-22 12:54:31"/>
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				<properties name="03 - Genotype overview" type="Logical" documentation="Genotypes (Assayed_genomic_genotype) produced over markers (Genomic_variation) and samples (Abstract_observation_target) under specific experimental conditions (Run). Latent_genotype has set of alleles (Genomic_allele) depending on ploidy level. &#xA;&#xA;Genotyping assay can detect different genotypes from different individuals. One genotype is measured from one individual at given marker site.   Genotypes may be stored with or without assay information (Variation assay is PCR (Polymerase Chain Reaction) assay designed for the variation site)  &#xA;"/>
				<project author="muilu" version="1.0" created="2007-10-12 16:34:47" modified="2009-08-06 11:36:39"/>
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				<properties name="08 - Sequence" type="Logical" documentation="All sequences inherit from a generic Sequence class. All sequences (Sequence) and sequence  features (e.g. Genomic_variation) can be located within a genomic sequence (Reference_genomic_sequence). This is modeled by common inheritance from an abstract superclass Locatable that can have several locations (Genomic_reference_location).  &#xA;&#xA;A Reference_genomic_landmark is any accessioned sequence within Reference_genomic_assembly. The model allows for multiple assemblies.  Any location within a landmark and therefore in an assembly is called Reference_genomic_location. Any variable site in an assembly is a Genomic_polymorphism. The variable sequences within Genomic_variations are called Genomic_alleles. &#xA;"/>
				<project author="muilu" version="1.0" created="2008-01-29 14:27:05" modified="2009-08-06 12:40:31"/>
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				<properties name="02 - Sample" type="Logical" documentation="An individual (Individual) interacts with the rest of the model by giving one or more samples (Molecular_samples) from different tissues.  Mixed samples and more complicated sample organisations are modelled by allowing  Molecular_samples and Panels be composed of multiples of themselves. In these cases it is common that individuals can not be identified. &#xA;&#xA;An individual (Individual) has parent IDs as attributes. This information makes it possible to reconstruct pedigrees when needed. A taxon identifies the taxonomic group, typically species, the individual or the population sample belongs to. Further, they can be placed on a geographic  map (Geographic_location)&#xA;"/>
				<project author="muilu" version="1.0" created="2008-01-29 14:28:45" modified="2009-08-05 20:22:09"/>
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				<properties name="07 - Haplotype" type="Logical" documentation="Haplotype  (Genomic_haplotype) is a set of  polymorphisms (Genomic alleles) on a single chromosome (chromatid). Haplotypes may be grouped  into sets like haplotype blocks (Haplotype_block) separated by recombination regions and gene based haplotype (Gene_based_haplotype), which combines sets of haplotypes  on same gene structure.&#xA;&#xA;Depending on an assay used, a genotype (Consensus_genomic_genotype) may contain  information about the phase of the detected Genomic_alleles. Alternatively,  various additional methods (Haplotype_derivation_methods) can be used to measure or  calculate haplotypes (Genomic_haplotypes) from the genotype data.   The aim of many haplotype studies is to find haplotypes within a given sequence region that  define most of the variation in populations (Set_of_haplotypes). Haplotype blocks (Haplotype_blocks) are clusters determined by linkage disequilibrium-based methods. The &#xA;other common way to define clusters is use a the sequence region of the gene (Gene_based_haplotype). &#xA;"/>
				<project author="muilu" version="1.0" created="2008-01-29 14:44:33" modified="2009-08-06 12:15:27"/>
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				<properties name="09 - Map" type="Logical" documentation="A map organizes genomic features and assigns them locations. The primary maps (Physical_map, Sequence_map) which have additive sequence residue count distances between  markers, are separated here from secondary maps (Ordered_map) which at best can only deal  with non-metric distances. For each type a map (Map) there is a  corresponding location (Location). Hence a marker (Genetic_variation) can have several locations (Reference_genomic_location) in sequences (Reference_genomic_landmark) and additionally  be located within a band (Cytogenetic_location) in a species-specific  karyotype  (Cytogenetic_map) as well as in (Genetic_location) several genetic maps (Genetic_map), e.g. in  maps based on male and female recombination frequencies. Genomic assembly (Reference_genomic_assembly) is a physical sequence map which is combination of genomic sequence(Reference_genomic_landmark). Feature locations can also be expressed in  chromosomal locations in an assembly(Reference_genomic_location_in_assembly).  &#xA;"/>
				<project author="muilu" version="1.0" created="2008-01-29 14:45:50" modified="2009-08-06 12:45:32"/>
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