{"id":1741,"date":"2025-06-06T17:07:04","date_gmt":"2025-06-06T21:07:04","guid":{"rendered":"https:\/\/scienceweb.clemson.edu\/chg\/?page_id=1741"},"modified":"2026-02-06T14:07:20","modified_gmt":"2026-02-06T19:07:20","slug":"genomics-core","status":"publish","type":"page","link":"https:\/\/scienceweb.clemson.edu\/ihg\/research-cores\/genomics-core\/","title":{"rendered":"Genomics Core"},"content":{"rendered":"

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IHG Genomics Core<\/h1>\n

[\/et_pb_text][et_pb_text _builder_version=”4.27.5″ text_font=”–et_global_body_font||||||||” text_text_color=”#ffffff” text_font_size=”20px” text_line_height=”1.2em” custom_padding=”||0px|||” locked=”off” global_colors_info=”{}”]<\/p>\n

The Genomics Core delivers end-to-end genomics support using state-of-the-art sequencing technologies, including the Illumina NovaSeq X+, PacBio Revio, ONT PromethION P2 Integrated, and 10x Genomics Chromium iX. Our expert staff partner with investigators from study design through data generation to support a wide range of applications, including whole-genome sequencing, RNA-seq, ATAC-seq, single-cell, and other high-throughput genomics assays. We also offer wet lab training courses and seminars to give users hands-on experience.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ disabled_on=”|on|on” admin_label=”Hero” _builder_version=”4.27.4″ use_background_color_gradient=”on” background_color_gradient_stops=”rgba(71,74,182,0.27) 0%|#322e66 100%” background_color_gradient_start=”rgba(71,74,182,0.27)” background_color_gradient_end=”#322e66″ background_image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/07\/facility2.jpg” background_position=”top_center” background_blend=”overlay” custom_padding=”|0px||0px” animation_style=”slide” animation_direction=”top” animation_intensity_slide=”2%” global_colors_info=”{}”][et_pb_row _builder_version=”4.16″ background_size=”initial” background_position=”top_left” background_repeat=”repeat” custom_width_px=”1280px” global_colors_info=”{}” button_one_text_size__hover_enabled=”off” button_one_text_size__hover=”null” button_two_text_size__hover_enabled=”off” button_two_text_size__hover=”null” button_one_text_color__hover_enabled=”on” button_one_text_color__hover=”#3550a0″ button_two_text_color__hover_enabled=”on” button_two_text_color__hover=”#ffffff” button_one_border_width__hover_enabled=”off” button_one_border_width__hover=”null” button_two_border_width__hover_enabled=”off” button_two_border_width__hover=”null” button_one_border_color__hover_enabled=”off” button_one_border_color__hover=”null” button_two_border_color__hover_enabled=”off” button_two_border_color__hover=”null” button_one_border_radius__hover_enabled=”off” button_one_border_radius__hover=”null” button_two_border_radius__hover_enabled=”off” button_two_border_radius__hover=”null” button_one_letter_spacing__hover_enabled=”off” button_one_letter_spacing__hover=”null” button_two_letter_spacing__hover_enabled=”off” button_two_letter_spacing__hover=”null” button_one_bg_color__hover_enabled=”on” button_one_bg_color__hover=”rgba(255,255,255,0.8)” button_two_bg_color__hover_enabled=”on” button_two_bg_color__hover=”rgba(255,255,255,0.3)”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_divider color=”rgba(126,190,197,0)” divider_style=”none” divider_position=”center” divider_weight=”0″ _builder_version=”4.16″ height=”6px” custom_margin=”100px||100px|” global_colors_info=”{}”][\/et_pb_divider][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ disabled_on=”|on|on” admin_label=”Hero” _builder_version=”4.16″ background_color=”#8300e9″ use_background_color_gradient=”on” background_color_gradient_stops=”rgba(71,74,182,0.27) 0%|#322e66 100%” background_color_gradient_start=”rgba(71,74,182,0.27)” background_color_gradient_end=”#322e66″ background_position=”top_center” background_blend=”overlay” custom_padding=”10px|0px|10px|0px” animation_style=”slide” animation_direction=”top” animation_intensity_slide=”2%” global_colors_info=”{}”][et_pb_row _builder_version=”4.16″ background_size=”initial” background_position=”top_left” background_repeat=”repeat” custom_width_px=”1280px” global_colors_info=”{}” button_one_text_size__hover_enabled=”off” button_one_text_size__hover=”null” button_two_text_size__hover_enabled=”off” button_two_text_size__hover=”null” button_one_text_color__hover_enabled=”on” button_one_text_color__hover=”#3550a0″ button_two_text_color__hover_enabled=”on” button_two_text_color__hover=”#ffffff” button_one_border_width__hover_enabled=”off” button_one_border_width__hover=”null” button_two_border_width__hover_enabled=”off” button_two_border_width__hover=”null” button_one_border_color__hover_enabled=”off” button_one_border_color__hover=”null” button_two_border_color__hover_enabled=”off” button_two_border_color__hover=”null” button_one_border_radius__hover_enabled=”off” button_one_border_radius__hover=”null” button_two_border_radius__hover_enabled=”off” button_two_border_radius__hover=”null” button_one_letter_spacing__hover_enabled=”off” button_one_letter_spacing__hover=”null” button_two_letter_spacing__hover_enabled=”off” button_two_letter_spacing__hover=”null” button_one_bg_color__hover_enabled=”on” button_one_bg_color__hover=”rgba(255,255,255,0.8)” button_two_bg_color__hover_enabled=”on” button_two_bg_color__hover=”rgba(255,255,255,0.3)”][et_pb_column type=”4_4″ _builder_version=”4.16″ custom_padding=”|||” global_colors_info=”{}” custom_padding__hover=”|||”][et_pb_text _builder_version=”4.27.4″ text_font_size=”26px” text_line_height=”1.2em” header_font=”|on|||” header_font_size=”26px” header_line_height=”1.2em” background_layout=”dark” custom_padding=”|||” header_font_size_last_edited=”off|desktop” locked=”off” global_colors_info=”{}”]<\/p>\n

IHG Genomics Core<\/h1>\n

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The Genomics Core delivers end-to-end genomics support using state-of-the-art sequencing technologies, including the Illumina NovaSeq X+, PacBio Revio, ONT PromethION P2 Integrated, and 10x Genomics Chromium iX. Our expert staff partner with investigators from study design through data generation to support a wide range of applications, including whole-genome sequencing, RNA-seq, ATAC-seq, single-cell, and other high-throughput genomics assays. We also offer wet lab training courses and seminars to give users hands-on experience.<\/span><\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Courses” _builder_version=”4.27.4″ custom_padding=”0px|0px|0px|0px||” global_colors_info=”{}”][et_pb_row column_structure=”2_3,1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”2_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/scienceweb.clemson.edu\/ihg\/wp-content\/uploads\/sites\/4\/2026\/02\/IMG_9170-scaled-1-1.jpg” alt=”A woman with dark hair and in glasses dressed in black standing next to a purple banner that says Clemson Center for Human Genetics” title_text=”Genomics Core Staff” _builder_version=”4.27.5″ _module_preset=”default” custom_padding=”|0px||||” hover_enabled=”0″ global_colors_info=”{}” sticky_enabled=”0″][\/et_pb_image][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.27.5″ _module_preset=”default” text_font=”–et_global_body_font||||||||” text_font_size=”20px” header_font_size=”37px” header_2_font=”–et_global_heading_font||||||||” text_orientation=”center” min_height=”220.9px” custom_margin=”204px|||-90px||” custom_padding=”||0px|||” hover_enabled=”0″ global_colors_info=”{}” sticky_enabled=”0″]<\/p>\n

Meet the Genomics Core!<\/strong><\/h2>\n

Ms. Kaitlyn Williams, M.S. (pictured left) directs the Clemson University Institute for Human Genetics Genomics Core. She hold a total of 10 years of molecular wet lab experience!<\/p>\n

Our Core provides comprehensive services for every stage of next-generation sequencing, including extraction, library preparation, and quality control. We are happy to consult with you about your project, and help design your experiment!<\/p>\n

 <\/p>\n

[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_heading title=”Comprehensive Genetic Equipment” _builder_version=”4.27.4″ _module_preset=”c33f07d9-41e0-421a-8799-5799df695cce” title_level=”h2″ title_font=”–et_global_heading_font|IBM Plex Sans Condensed_weight|||||||” title_text_align=”center” title_text_color=”#0e0c19″ title_font_size=”50px” title_line_height=”1.2em” custom_margin=”||10px||false|false” title_font_size_tablet=”28px” title_font_size_phone=”20px” title_font_size_last_edited=”on|phone” global_colors_info=”{}”][\/et_pb_heading][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_3,1_3,1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb title=”PacBio Revio” image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/06\/REVIORESIZED.png” alt=”Black PacBio Revio Long Read Sequencer with white interior, robotic arm, vertical sliding door, and pink branding at the bottom.
\n” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ header_text_align=”center” body_text_align=”center” global_colors_info=”{}”]<\/p>\n

The Genomics Core offers sequencing services using the PacBio Revio, a high-throughput long-read sequencing platform that delivers highly accurate HiFi reads averaging 15\u201320 kb with over 90% of bases at Q30+ accuracy. Ideal for applications such as whole-genome sequencing, transcriptome analysis, and structural variant detection, the Revio can generate up to 1.4 terabases of data per day\u2014supporting up to 1,300 human genomes per year at 30\u00d7 coverage.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb title=”Illumina NovaSeq X+” image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/06\/IlluminaRESIZED-1.png” alt=”White\/silver laboratory instrument with rectangular housing, digital display screen on top showing time readings, and blue illuminated oval window in the center of the front panel.*” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ header_text_align=”center” global_colors_info=”{}”]<\/p>\n

The Genomics Core offers sequencing services using the Illumina NovaSeq X+, a state-of-the-art high-throughput platform capable of generating up to 16 Tb of data in under 48 hours. This system delivers exceptional accuracy, scalability, and cost-efficiency, making it ideal for large-scale projects such as whole-genome, single-cell, and transcriptome sequencing. Let us help power your next big discovery.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb title=”ONT PromethION 2 Integrated (P2i)” image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/06\/NANOPORERESIZED.png” alt=”Black Oxford Nanopore PromethION 2 with front mesh panel, tilted touchscreen showing circular data, and logo on the side.” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ header_text_align=”center” text_orientation=”center” global_colors_info=”{}”]<\/p>\n

The Genomics Core offers access to the Oxford Nanopore PromethION 2 Integrated (P2i), a compact benchtop sequencer built for medium-to-high-throughput projects. With two high-output flow cell positions and powerful onboard computing, the P2i enables real-time long-read sequencing of DNA and direct RNA. It supports advanced features like basecalling, methylation detection, demultiplexing, and alignment\u2014ideal for whole-genome sequencing, transcriptomics, and microbiome research.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_3,1_3,1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb title=”10X Genomics Chromium iX” image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/06\/SINGLE-CELL.png” alt=”Laboratory setup with a grey vortex mixer (top left), a compact white-and-black cell counter (top right), and a large 10X Genomics Chromium iX system with touchscreen (bottom).” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ header_text_align=”center” body_text_align=”center” global_colors_info=”{}”]<\/p>\n

Our Genomics Core offers three cutting-edge single-cell sequencing platforms: the 10X Genomics Chromium iX system, Illumina Single Cell equipment, and Parse Biosciences technology, providing versatile options for high-throughput and precise transcriptomic profiling. We use the Countess 3 Fluorescent Cell Counter to accurately assess cell and nuclei concentration and viability, ensuring high-quality samples for all workflows. Together, these state-of-the-art technologies enable comprehensive exploration of cellular heterogeneity with confidence and flexibility.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb title=”Fragment Analyzer” image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/06\/FRAGRESIZED.png” alt=”White Agilent Fragment Analyzer with six black-handled drawers on the left, a blue logo at the top, and a smooth right panel.” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ header_text_align=”center” body_text_align=”center” global_colors_info=”{}”]<\/p>\n

We are excited to offer nucleic acid analysis using our in-house Agilent Technologies Fragment Analyzer (12-sample version). This advanced system provides high-resolution sizing and quantification of DNA and RNA, including total RNA, genomic DNA, and NGS libraries. With reliable quality metrics like RQN and GQN, it ensures accurate and consistent sample assessment for your research needs.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][et_pb_column type=”1_3″ _builder_version=”4.27.4″ _module_preset=”default” global_colors_info=”{}”][et_pb_blurb title=”Opentrons Flex” image=”https:\/\/scienceweb.clemson.edu\/chg\/wp-content\/uploads\/sites\/4\/2025\/06\/OTFLEX.png” alt=”Black and gray Opentrons Flex robot with a cubic frame, transparent panels, visible pipetting head, and blue module spots on the deck.
\n” _builder_version=”4.27.4″ _module_preset=”default” header_level=”h3″ header_font=”–et_global_heading_font||||||||” header_text_align=”center” body_font=”–et_global_body_font||||||||” global_colors_info=”{}”]<\/p>\n

The Genomics Core now offers advanced automation capabilities with our in-house Opentrons Flex liquid handling robot. In addition to supporting high-throughput genomics workflows, the Flex is equipped to shear high molecular weight (HMW) DNA\u2014ideal for preparing samples for long-read sequencing. This enables faster, more consistent processing for a wide range of applications.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Services” _builder_version=”4.18.0″ _module_preset=”default” locked=”off” collapsed=”on” global_colors_info=”{}”][et_pb_row _builder_version=”4.18.0″ _module_preset=”5138c454-be54-4233-bd3b-f8e6a8747976″ custom_margin=”|auto|-10px|auto|false|false” locked=”off” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.18.0″ _module_preset=”73121f80-a3ef-4484-8763-c3f18e3c56d2″ global_colors_info=”{}”][et_pb_heading title=”Comprehensive Genetic Services” _builder_version=”4.27.4″ _module_preset=”c33f07d9-41e0-421a-8799-5799df695cce” title_level=”h2″ title_font=”–et_global_heading_font|IBM Plex Sans Condensed_weight|||||||” title_text_align=”center” title_text_color=”#0e0c19″ title_font_size=”50px” title_line_height=”1.2em” custom_margin=”||10px||false|false” title_font_size_tablet=”28px” title_font_size_phone=”20px” title_font_size_last_edited=”on|phone” global_colors_info=”{}”][\/et_pb_heading][et_pb_heading title=”Our Expertise in Genetics” _builder_version=”4.27.4″ _module_preset=”f0c675ea-2574-4d0e-b725-30f8550a8550″ title_level=”h3″ title_font=”–et_global_heading_font|IBM Plex Sans Condensed_weight||on|||||” title_text_align=”center” title_text_color=”#522d80″ title_font_size=”14px” title_letter_spacing=”1px” title_line_height=”1.4em” custom_margin=”||10px||false|false” title_font_size_tablet=”13px” title_font_size_phone=”13px” title_font_size_last_edited=”on|desktop” global_colors_info=”{%22#22577a%22:%91%22title_text_color%22%93}”][\/et_pb_heading][\/et_pb_column][\/et_pb_row][et_pb_row column_structure=”1_4,1_4,1_4,1_4″ custom_padding_last_edited=”on|tablet” _builder_version=”4.27.4″ _module_preset=”5138c454-be54-4233-bd3b-f8e6a8747976″ custom_padding_tablet=”||0px||false|false” custom_padding_phone=”||0px||false|false” global_colors_info=”{}”][et_pb_column type=”1_4″ _builder_version=”4.27.4″ _module_preset=”73121f80-a3ef-4484-8763-c3f18e3c56d2″ global_colors_info=”{}”][et_pb_blurb title=”DNA, RNA, & High Molecular Weight DNA Extraction” use_icon=”on” font_icon=”||fa||900″ icon_placement=”left” image_icon_width=”32px” content_max_width=”100%” _builder_version=”4.27.4″ _module_preset=”212b201d-2c34-41bd-936c-851b7357d08b” header_font=”–et_global_heading_font|600|||||||” header_text_color=”#0e0c19″ header_font_size=”18px” header_line_height=”1.4em” body_font=”–et_global_body_font|IBM Plex Sans_weight|||||||” body_text_color=”#3c3a47″ body_font_size=”16px” body_line_height=”1.75em” body_link_text_color=”#22577a” body_link_font_size=”14px” background_mask_style=”arch” image_icon_custom_margin=”||||false|false” image_icon_custom_padding=”||||false|false” custom_padding=”||7px|||” animation=”off” header_font_size_tablet=”15px” header_font_size_phone=”13px” header_font_size_last_edited=”on|phone” body_font_size_tablet=”15px” body_font_size_phone=”14px” body_font_size_last_edited=”on|desktop” border_radii_image=”on|6px|6px|6px|6px” global_colors_info=”{%22#3c3a47%22:%91%22body_text_color%22,%22body_text_color%22%93,%22#0e0c19%22:%91%22header_text_color%22,%22header_text_color%22%93,%22#57cc99%22:%91%22icon_color%22%93}”]<\/p>\n

Providing reliable nucleic acid extractions from diverse sample types and organisms in our BSL-2 lab, with expert consultation for user-performed extractions and cell\/nuclei isolation.<\/p>\n

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Delivering short- and long-read whole genome sequencing with Illumina, PacBio, and ONT, with cost-effective strategies, expert library prep, and consultation support.<\/p>\n

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Providing expert RNA sequencing with rRNA depletion, polyA enrichment, and advanced long-read options via PacBio Kinnex and ONT Direct RNA.<\/p>\n

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Delivering comprehensive single-cell sequencing\u2014including RNA-seq, ATAC-seq, and Multiome\u2014on cutting-edge platforms like 10x Genomics, Parse, and Illumina, with tailored, cost-effective solutions aligned to your research goals.<\/p>\n

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Providing bulk ATAC-seq library preparation with the reliable Zymo-Seq ATAC Kit, delivering high-quality chromatin accessibility profiling and expert support for streamlined, consistent results.<\/p>\n

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Delivering comprehensive quality control for nucleic acids and sequencing libraries using advanced tools like Nanopore, Qubit, Fragment Analyzer, TapeStation, and KAPA qPCR, ensuring your samples meet the highest standards.<\/p>\n

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Providing next-generation sequencing on Illumina, PacBio, and ONT platforms, delivering versatile and high-quality data tailored to your research needs.<\/p>\n

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Offering expert consultation for experimental design, nuclei and cell isolation, and all your genomics needs to ensure successful and customized research outcomes.<\/p>\n

[\/et_pb_blurb][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=”1″ admin_label=”Call to Action” _builder_version=”4.27.4″ _module_preset=”default” background_color=”#522d80″ custom_padding=”10px||10px||true|false” locked=”off” collapsed=”on” global_colors_info=”{%22#22577a%22:%91%22background_color%22%93}”][et_pb_row column_structure=”2_3,1_3″ _builder_version=”4.24.2″ _module_preset=”5138c454-be54-4233-bd3b-f8e6a8747976″ global_colors_info=”{}”][et_pb_column type=”2_3″ _builder_version=”4.18.0″ _module_preset=”73121f80-a3ef-4484-8763-c3f18e3c56d2″ global_colors_info=”{}”][et_pb_blurb title=”Connect with Our Experts” use_icon=”on” font_icon=”||fa||900″ icon_color=”#FFFFFF” icon_placement=”left” image_icon_width=”40px” content_max_width=”100%” _builder_version=”4.27.4″ _module_preset=”ca79a742-981f-479f-a8a2-3a0292efaff0″ header_level=”h2″ header_font=”–et_global_heading_font|IBM Plex Sans Condensed_weight|||||||” header_text_color=”#FFFFFF” header_font_size=”18px” header_line_height=”1.4em” body_font=”–et_global_body_font|IBM Plex Sans_weight|||||||” body_text_color=”#FFFFFF” body_font_size=”16px” body_line_height=”1.75em” body_link_font=”||||on||||” body_link_text_color=”#FFFFFF” body_link_font_size=”14px” background_mask_style=”arch” animation=”off” header_font_size_tablet=”15px” header_font_size_phone=”14px” header_font_size_last_edited=”on|phone” body_font_size_tablet=”15px” body_font_size_phone=”14px” body_font_size_last_edited=”on|desktop” border_radii_image=”on|6px|6px|6px|6px” global_colors_info=”{%22gcid-f2943306-fa6c-45f0-b632-5fc00151366a%22:%91%22button_text_color%22%93,%22gcid-36fd78a7-34bc-404d-873c-dafa34efaae5%22:%91%22button_text_color%22%93}”]<\/p>\n

Ready to explore how our Genomics core can benefit your research? Reach out today to schedule a consultation with our team and discover the possibilities.<\/p>\n

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IHG Genomics CoreThe Genomics Core delivers end-to-end genomics support using state-of-the-art sequencing technologies, including the Illumina NovaSeq X+, PacBio Revio, ONT PromethION P2 Integrated, and 10x Genomics Chromium iX. Our expert staff partner with investigators from study design through data generation to support a wide range of applications, including whole-genome sequencing, RNA-seq, ATAC-seq, single-cell, and […]<\/p>\n","protected":false},"author":32,"featured_media":0,"parent":1747,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-1741","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/pages\/1741","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/users\/32"}],"replies":[{"embeddable":true,"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/comments?post=1741"}],"version-history":[{"count":0,"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/pages\/1741\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/pages\/1747"}],"wp:attachment":[{"href":"https:\/\/scienceweb.clemson.edu\/ihg\/wp-json\/wp\/v2\/media?parent=1741"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}