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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/991343.rdf" xlink:actuate="onRequest">Annotated genome of Nucella lapillus (Atlantic dog whelk) collected from Nahant, MA in May 2024</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Ford, M., Vollmer, S. V., Trussell, G. C. (2026) Annotated genome of Nucella lapillus (Atlantic dog whelk) collected from Nahant, MA in May 2024. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2026-03-23 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.991343.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Atlantic dog whelk (Nucella lapillus) genome Dataset Description: &amp;lt;p&amp;gt;&amp;lt;em&amp;gt;Nucella lapillus&amp;lt;/em&amp;gt; is an important player in rocky shore food chains and has been a focal organism of ecological and evolutionary studies for decades. Despite poor dispersal, they have a broad geographic range, which makes them an ideal species to examine isolation by distance and selection across environmental gradients. &amp;amp;nbsp;A fully annotated genome of &amp;lt;em&amp;gt;N. lapillus&amp;lt;/em&amp;gt; generated with Oxford Nanopore Technology (ONT) sequencing at ∼37× coverage was described in detail in the following publication:&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Ford, M. R., Vollmer, S. V., &amp;amp;amp; Trussell, G. C. (2025). Annotated genome of the Atlantic dog whelk, Nucella lapillus. G3: Genes, Genomes, Genetics, 15(10). https://doi.org/10.1093/g3journal/jkaf182&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;This dataset provides information on the study and includes links to the genetic dataset at the National Center for Biotechnology Information (NCBI) BioProject PRJNA1238877.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Sample collection and DNA extraction&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
An adult &amp;lt;em&amp;gt;Nucella lapillus&amp;lt;/em&amp;gt; individual was collected in May 2024 from Nahant, MA (42.419732, −70.902171). The foot tissue was used for DNA extraction and isolation.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;High molecular weight (HMW) DNA was extracted from the foot via the CTAB method (1.4 M NaCl&amp;amp;nbsp;and 2% CTAB), followed by three chloroform reactions. The complete&amp;amp;nbsp;extraction protocol is available on the project GitHub repository (https://github.com/meghanclownfish/Nucella-lapillus-genome/tree/main/1_extraction). The HMW DNA was precipitated in ethanol (EtOH) and resuspended in Tris-EDTA buffer. The sample was further purified using a Genomic DNA Clean and Concentrator kit (gDCC-10, ZYMO Research, Irvine, CA, USA) per manufacturer’s instructions. Sample quality and concentration were assessed by running 2 μL of the sample on NanoDrop (Thermo Fisher Scientific, Singapore). A sample was deemed ready for sequencing if the&amp;amp;nbsp;260/280 ratio was ∼1.9 and the&amp;amp;nbsp;260/230 ratio fell between 2.0 and 2.2, following Sun et al. 2020.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
&amp;lt;strong&amp;gt;Library prep and sequencing&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
&amp;lt;em&amp;gt;N. lapillus&amp;lt;/em&amp;gt; long reads were sequenced using ONT platforms and libraries were prepared with the ONT Ligation sequencing kit (SQK-LSK114, ONT, Oxford, UK) and NEBNext Companion Module (E7180S NEB). Standard manufacturer's protocol was implemented with a few exceptions (see Ford et al., 2025 for details). Sequencing was done on a PromethION. Six flow cells in total were used to generate 103,553,219,099 bp raw data. PromethION flow cells (FLO-PRO114M) were primed and loaded per the standard manufacturer's protocol. To increase the yield of each flow cell, runs were paused and flushed using the EXP-WSH004 (ONT) kit and reloaded. High quality base calling was performed with Dorado 0.7.1 (ONT).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;Genome size and heterozygosity&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
Genome size was estimated using JELLYFISH v2.2.10 to count canonical 41-mers from high quality ONT reads (min quality: 5) and computed a histogram of k-mer occurrence (Marcais and Kingsford 2011). The histogram was used to estimate heterozygosity with GenomeScope (Ranallo-Benavidez et al. 2020).&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/816469.rdf" xlink:title="OCE-2017626" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2017626 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2017626</gmx:Anchor>
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Over the past two decades, the Gulf of Maine has experienced unprecedented warming that, among other things, has further enabled the invasive green crab to expand its range in rocky shore habitats. The adverse ecological impacts of this invasive predator have been documented worldwide. This study examines how geographic variation in the capacity of two common prey species to respond to the combination of this predator and warming ocean temperatures can shape prey feeding and performance and impact community structure and dynamics. Hence, this research enhances understanding of the evolution of phenotypes, their plasticity, and the nature of adaptation and its role in eco-evolutionary dynamics. More broadly, it informs understanding of how organisms and marine communities may respond to future environmental change. In addition, this project makes contributions to the STEM pipeline by providing middle and high school, undergraduate, and graduate students with cross-disciplinary training in evolutionary and community ecology. In collaboration with an institutional outreach program, the investigator is also developing web-based multimedia projects and teacher resource materials based on this research.&lt;/p&gt;
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http://lod.bco-dmo.org/id/dataset-parameter/995349.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995350.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995351.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995352.rdf
	Name: End
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http://lod.bco-dmo.org/id/dataset-parameter/995354.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995357.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995358.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995360.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995361.rdf
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http://lod.bco-dmo.org/id/dataset-parameter/995362.rdf
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&amp;lt;p&amp;gt;High molecular weight (HMW) DNA was extracted from the foot via the CTAB method (1.4 M NaCl&amp;amp;nbsp;and 2% CTAB), followed by three chloroform reactions. The complete&amp;amp;nbsp;extraction protocol is available on the project GitHub repository (https://github.com/meghanclownfish/Nucella-lapillus-genome/tree/main/1_extraction). The HMW DNA was precipitated in ethanol (EtOH) and resuspended in Tris-EDTA buffer. The sample was further purified using a Genomic DNA Clean and Concentrator kit (gDCC-10, ZYMO Research, Irvine, CA, USA) per manufacturer’s instructions. Sample quality and concentration were assessed by running 2 μL of the sample on NanoDrop (Thermo Fisher Scientific, Singapore). A sample was deemed ready for sequencing if the&amp;amp;nbsp;260/280 ratio was ∼1.9 and the&amp;amp;nbsp;260/230 ratio fell between 2.0 and 2.2, following Sun et al. 2020.&amp;lt;br /&amp;gt;
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- Added fields for Latitude, Longitude, Habitat, Tissue_type, Sampling_Date, and Specimen_type to both tables
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- Renamed fields/column headings to conform with BCO-DMO naming conventions and improve interoperability. 
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