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        <gco:CharacterString>Dataset Description: &amp;lt;p&amp;gt;Acronyms:&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
SNP = Single-nucleotide Polymorphism&amp;lt;br /&amp;gt;
MLA = Machine Learning Algorithm&amp;lt;br /&amp;gt;
LD = Linkage Disequilibrium&amp;lt;br /&amp;gt;
NCBI = National Center for Biotechnology Information&amp;lt;br /&amp;gt;
DNA = Deoxyribonucleic acid&amp;lt;br /&amp;gt;
MVP = Model Validation Program&amp;lt;br /&amp;gt;
ABC = Aquaculture Genetics and Breeding Technology Center&amp;lt;br /&amp;gt;
VIMS = Virginia Institute of Marine Science&amp;amp;nbsp;&amp;lt;br /&amp;gt;
GO = Gene Ontology&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Source populations for monoculture treatments included six wild populations and two proprietary broodstock lines (DEBY and LOLA) from the Aquaculture Genetics and Breeding Technology Center (ABC), Virginia Institute of Marine Science (VIMS). Wild populations spanned the species’ native range, which is structured into distinct genetic clusters separated by the Florida peninsula (Reeb &amp;amp;amp; Avise, 1990, Puritz et al., 2022). Populations included oysters from: a variable salinity site in Texas (W1-TX), a low salinity site in Louisiana (W2-LA), a high salinity site on the east coast of Florida (W3-FL), a moderate salinity site in the James River, Virginia (W4-VA), a variable salinity site in New Hampshire (W5-NH), and a high salinity site in Maine (W6-ME). W4-VA was considered local to both common garden sites due to its geographic proximity and intermediate salinity.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Gill tissue was collected from each parent (&amp;lt;em&amp;gt;n&amp;lt;/em&amp;gt; = 160) after spawning and stored in 95% ethanol at -80°C. DNA was extracted using the Qiagen DNeasy Blood and Tissue Kit and shipped to Neogen Genomics (Lincoln, NE) for genotyping on a 200K ThermoFisher Affymetrix Axiom SNP array derived from a 600K array (Gómez-Chiarri et al., 2015; Guo et al., 2023; Modak et al., 2021; Puritz et al., 2024) aligned to the haplotig-masked &amp;lt;em&amp;gt;Crassostrea virginica&amp;lt;/em&amp;gt; reference genome (C_virginica-3.0, GCA_002022765.4).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Raw genotypes were processed and filtered in R v4.4.2 (R Core Team 2025). Missing SNPs were imputed using LEA v3.6.0 (Frichot &amp;amp;amp; François, 2015) with K = 2 ancestral groups to produce a full SNP set. We thinned SNPs for linkage disequilibrium (LD) for population structure analysis and neutral parameterization of genome scans (Lotterhos, 2019) using bigsnpr v1.11.3 (Privé et al., 2018). The archived genotype matrix contains the processed, imputed genotype calls per individual encoded in 0/1/2 integer format (homozygous reference, heterozygous, and homozygous alternate, respectively). The accompanying SNP metadata file provides per-locus descriptions including genomic position, gene identifiers, functional descriptions, Gene Ontology terms, and population genetic statistics derived from OutFLANK (FST, expected heterozygosity, p-values, q-values, and outlier flags), as well as a flag indicating inclusion in the LD-thinned dataset, enabling straightforward filtering for only LD-thinned SNPs.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/876609.rdf" xlink:title="OCE-2043905" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2043905 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2043905</gmx:Anchor>
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Environmental change can be rapid and involve multiple aspects of the environment changing at the same time, such as warming and increased disease pressure. Rapid environmental change threatens the productivity of aquaculture and crops on which humans depend. Predicting organisms' vulnerabilities to rapid and multifactor environmental change, however, is a major scientific challenge. A hurdle to addressing this challenge arises from the complex and non-intuitive ways that organisms adapt, through changes at the level of the DNA sequence, to many environmental stresses at the same time. Thus, there is a need for new approaches to understand and predict adaptation in multivariate environments. To address this need, this project integrates research and education with a Model Validation Program (MVP). The research is developing and evaluating Machine Learning Algorithms (MLAs) for understanding and predicting adaptation of organisms to multivariate environments from their DNA sequences. To evaluate MLAs, this research combines both data simulation and an empirical test in the field with the Eastern Oyster, which provide important ecosystem services and support a multi-million dollar industry. For oysters, this research is studying how temperature, disease pressure, and salinity interact with evolutionary history to determine fitness in the field. This research advances efforts toward addressing the major scientific challenge of predicting adaptation in complex environments by integrating concepts across the frontiers of marine, evolutionary, and statistical sciences in a new way. Machine learning and model validation are not traditionally taught in the marine and environmental sciences, but are becoming increasingly relevant to these fields. As part of a broader education program, this research is developing MVP Learning Modules for high school students and undergraduates, which help students build the foundational knowledge they need to critically evaluate and apply models. Modules are being disseminated to hundreds of students in the greater Boston area and are being made available online for widespread use. The MVP mentoring program is training graduate students, undergraduates, and high school students in marine evolutionary ecology, statistical genomics, and machine learning. This research addresses a pressing societal need to more informatively match genotypes to environments for restoration, farming, and assisted gene flow efforts. Results are being disseminated to stakeholders in the oyster industry.&lt;/p&gt;
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	Description: &lt;p&gt;Chromosomal position where SNP occurs on assembly GCF_002022765.2_C_virginica-3.0_genomic&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998841.rdf
	Name: FST
	Units: unitless
	Description: &lt;p&gt;Fixation index for the locus calculated by OutFLANK (Whitlock and Lotterhos 2015)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998842.rdf
	Name: He
	Units: unitless
	Description: &lt;p&gt;Expected heterozygosity for the locus calculated by OutFLANK (Whitlock and Lotterhos 2015)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998843.rdf
	Name: pvalues
	Units: unitless
	Description: &lt;p&gt;Two-tailed p-value for the test of neutrality for the locus calculated by OutFLANK (Whitlock and Lotterhos 2015)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998844.rdf
	Name: pvaluesRightTail
	Units: unitless
	Description: &lt;p&gt;Right-tailed p-value for the test of neutrality for the locus calculated by OutFLANK (Whitlock and Lotterhos 2015)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998845.rdf
	Name: qvalues
	Units: unitless
	Description: &lt;p&gt;q-value for the test of neutrality for the locus based on the right-tailed p-value calculated by OutFLANK (Whitlock and Lotterhos 2015)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998846.rdf
	Name: OutlierFlag
	Units: unitless
	Description: &lt;p&gt;True (T) or False (F) if the SNP was detected as an outlier by OutFLANK (Whitlock and Lotterhos 2015)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998847.rdf
	Name: gene_id
	Units: unitless
	Description: &lt;p&gt;Generic locus IDs (NCBI) for gene(s) where SNP occurs&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998848.rdf
	Name: gene_description
	Units: unitless
	Description: &lt;p&gt;Functional description(s) of gene(s) where SNP occurs&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998849.rdf
	Name: go_ids
	Units: unitless
	Description: &lt;p&gt;Unique seven-digit identifier for a gene ontology term&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998850.rdf
	Name: go_terms
	Units: unitless
	Description: &lt;p&gt;Description for a gene ontology term&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998851.rdf
	Name: SNPType
	Units: unitless
	Description: &lt;p&gt;K - G/T M - A/C R - A/G (most common) S - C/G (rarest) W - A/T Y - C/T (most common)&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998852.rdf
	Name: Tile_Std
	Units: unitless
	Description: &lt;p&gt;Affymetrix parameter for SNP chip design&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998853.rdf
	Name: Tile_max
	Units: unitless
	Description: &lt;p&gt;Affymetrix parameter for SNP chip design&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998854.rdf
	Name: Tile_v3
	Units: unitless
	Description: &lt;p&gt;SNPs tiled on the 200K chip&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998855.rdf
	Name: Replicates
	Units: unitless
	Description: &lt;p&gt;Affymetrix parameter for SNP chip design&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998856.rdf
	Name: Rank
	Units: unitless
	Description: &lt;p&gt;Affymetrix parameter for SNP chip design&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998857.rdf
	Name: Group
	Units: unitless
	Description: &lt;p&gt;pathogen detection CN probesets, content of Axiom_OysterCV, additional well-performing markers from screen&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998858.rdf
	Name: organism
	Units: unitless
	Description: &lt;p&gt;Genus species&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998859.rdf
	Name: cust_id
	Units: unitless
	Description: &lt;p&gt;Annotation&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998860.rdf
	Name: on_oystercv
	Units: unitless
	Description: &lt;p&gt;on Axiom_OysterCV developed be Breeding Consortium&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998861.rdf
	Name: mutID
	Units: unitless
	Description: &lt;p&gt;Mutation ID Affymetrix parameter for SNP chip design&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998862.rdf
	Name: chrom_position
	Units: unitless
	Description: &lt;p&gt;Chromosome location and position of SNP on the 200K array; separated by a &amp;#039;.&amp;#039;&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998863.rdf
	Name: scaffold
	Units: unitless
	Description: &lt;p&gt;Scaffold on assembly GCF_002022765.2_C_virginica-3.0_genomic&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998864.rdf
	Name: Sequence
	Units: unitless
	Description: &lt;p&gt;71mer sequence&lt;/p&gt; 
http://lod.bco-dmo.org/id/dataset-parameter/998865.rdf
	Name: thinned_dataset
	Units: unitless
	Description: &lt;p&gt;True or False if the SNP occurs in the linkage-disequilibrium thinned SNP dataset&lt;/p&gt; 
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&amp;lt;p&amp;gt;&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Gill tissue was collected from each parent (&amp;lt;em&amp;gt;n&amp;lt;/em&amp;gt; = 160) after spawning and stored in 95% ethanol at -80°C. DNA was extracted using the Qiagen DNeasy Blood and Tissue Kit and shipped to Neogen Genomics (Lincoln, NE) for genotyping on a 200K ThermoFisher Affymetrix Axiom SNP array derived from a 600K array (Gómez-Chiarri et al., 2015; Guo et al., 2023; Modak et al., 2021; Puritz et al., 2024) aligned to the haplotig-masked &amp;lt;em&amp;gt;Crassostrea virginica&amp;lt;/em&amp;gt; reference genome (C_virginica-3.0, GCA_002022765.4).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Raw genotypes were processed and filtered in R v4.4.2 (R Core Team 2025). Missing SNPs were imputed using LEA v3.6.0 (Frichot &amp;amp;amp; François, 2015) with K = 2 ancestral groups to produce a full SNP set. We thinned SNPs for linkage disequilibrium (LD) for population structure analysis and neutral parameterization of genome scans (Lotterhos, 2019) using bigsnpr v1.11.3 (Privé et al., 2018). The archived genotype matrix contains the processed, imputed genotype calls per individual encoded in 0/1/2 integer format (homozygous reference, heterozygous, and homozygous alternate, respectively). The accompanying SNP metadata file provides per-locus descriptions including genomic position, gene identifiers, functional descriptions, Gene Ontology terms, and population genetic statistics derived from OutFLANK (FST, expected heterozygosity, p-values, q-values, and outlier flags), as well as a flag indicating inclusion in the LD-thinned dataset, enabling straightforward filtering for only LD-thinned SNPs.&amp;lt;/p&amp;gt;</gco:CharacterString>
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- Renamed column &amp;quot;AX-ID&amp;quot; to &amp;quot;AX_ID&amp;quot;
- Set data types for all 29 columns: AX_ID, Affx_ID, Group, SNPType, Sequence, cust_id, gene_description, gene_id, go_ids, go_terms, mutID, on_oystercv, organism, scaffold, OutlierFlag, thinned_dataset as string; Chromosome, Position, Rank, Replicates, Tile_Std, Tile_max, Tile_v3 as integer; FST, He, chrom_position, pvalues, pvaluesRightTail, qvalues as number
- Output final table as &amp;quot;998738_v1_oyster-genotype-annotations.csv&amp;quot;

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