{"id":747,"date":"2022-05-16T15:20:49","date_gmt":"2022-05-16T15:20:49","guid":{"rendered":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/?page_id=747"},"modified":"2022-11-07T20:11:20","modified_gmt":"2022-11-07T20:11:20","slug":"science","status":"publish","type":"page","link":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/science\/","title":{"rendered":"Science"},"content":{"rendered":"<p>[et_pb_section bb_built=&#8221;1&#8243; inner_width=&#8221;auto&#8221; inner_max_width=&#8221;1080px&#8221;][et_pb_row][et_pb_column type=&#8221;1_2&#8243; custom_padding__hover=&#8221;|||&#8221; custom_padding=&#8221;|||&#8221;][et_pb_text _builder_version=&#8221;4.9.0&#8243; text_text_shadow_horizontal_length=&#8221;text_text_shadow_style,%91object Object%93&#8243; text_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; text_text_shadow_vertical_length=&#8221;text_text_shadow_style,%91object Object%93&#8243; text_text_shadow_vertical_length_tablet=&#8221;0px&#8221; text_text_shadow_blur_strength=&#8221;text_text_shadow_style,%91object Object%93&#8243; 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header_3_text_shadow_blur_strength=&#8221;header_3_text_shadow_style,%91object Object%93&#8243; header_3_text_shadow_blur_strength_tablet=&#8221;1px&#8221; header_4_text_shadow_horizontal_length=&#8221;header_4_text_shadow_style,%91object Object%93&#8243; header_4_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; header_4_text_shadow_vertical_length=&#8221;header_4_text_shadow_style,%91object Object%93&#8243; header_4_text_shadow_vertical_length_tablet=&#8221;0px&#8221; header_4_text_shadow_blur_strength=&#8221;header_4_text_shadow_style,%91object Object%93&#8243; header_4_text_shadow_blur_strength_tablet=&#8221;1px&#8221; header_5_text_shadow_horizontal_length=&#8221;header_5_text_shadow_style,%91object Object%93&#8243; header_5_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; header_5_text_shadow_vertical_length=&#8221;header_5_text_shadow_style,%91object Object%93&#8243; header_5_text_shadow_vertical_length_tablet=&#8221;0px&#8221; header_5_text_shadow_blur_strength=&#8221;header_5_text_shadow_style,%91object Object%93&#8243; header_5_text_shadow_blur_strength_tablet=&#8221;1px&#8221; header_6_text_shadow_horizontal_length=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; header_6_text_shadow_vertical_length=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_vertical_length_tablet=&#8221;0px&#8221; header_6_text_shadow_blur_strength=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_blur_strength_tablet=&#8221;1px&#8221; box_shadow_horizontal_tablet=&#8221;0px&#8221; box_shadow_vertical_tablet=&#8221;0px&#8221; box_shadow_blur_tablet=&#8221;40px&#8221; box_shadow_spread_tablet=&#8221;0px&#8221; vertical_offset_tablet=&#8221;0&#8243; horizontal_offset_tablet=&#8221;0&#8243; z_index_tablet=&#8221;0&#8243;]<\/p>\n<h3>What\u2019s Our Vision?<\/h3>\n<blockquote>\n<p>Give us <strong>your genome<\/strong>, and we will accurately predict your <strong>disease risks<\/strong> and <strong>drug targets<\/strong>\u2014so you can benefit from personalized diagnostics, prevention, and treatment.<\/p>\n<\/blockquote>\n<p>[\/et_pb_text][et_pb_image _builder_version=&#8221;4.9.0&#8243; 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header_4_text_shadow_blur_strength=&#8221;header_4_text_shadow_style,%91object Object%93&#8243; header_4_text_shadow_blur_strength_tablet=&#8221;1px&#8221; header_5_text_shadow_horizontal_length=&#8221;header_5_text_shadow_style,%91object Object%93&#8243; header_5_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; header_5_text_shadow_vertical_length=&#8221;header_5_text_shadow_style,%91object Object%93&#8243; header_5_text_shadow_vertical_length_tablet=&#8221;0px&#8221; header_5_text_shadow_blur_strength=&#8221;header_5_text_shadow_style,%91object Object%93&#8243; header_5_text_shadow_blur_strength_tablet=&#8221;1px&#8221; header_6_text_shadow_horizontal_length=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; header_6_text_shadow_vertical_length=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_vertical_length_tablet=&#8221;0px&#8221; header_6_text_shadow_blur_strength=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_blur_strength_tablet=&#8221;1px&#8221; box_shadow_horizontal_tablet=&#8221;0px&#8221; box_shadow_vertical_tablet=&#8221;0px&#8221; box_shadow_blur_tablet=&#8221;40px&#8221; box_shadow_spread_tablet=&#8221;0px&#8221; vertical_offset_tablet=&#8221;0&#8243; horizontal_offset_tablet=&#8221;0&#8243; z_index_tablet=&#8221;0&#8243;]<\/p>\n<h3><strong>How do we get there?\u00a0<\/strong><\/h3>\n<p><strong>Here are selected examples of the scientific research done by our team:\u00a0<\/strong><\/p>\n<blockquote>\n<p>We identified common risk variants in Alzheimer\u2019s disease (<strong>Nat Neuro 2017<\/strong>) and rare pathogenic variants in Cancer (<strong>Cell 2018<\/strong>) while leading national\/international genomics consortia projects.<\/p>\n<\/blockquote>\n<blockquote>\n<p>We specifically characterized genomes of patients from diverse ancestry populations (<strong>Cancer Cell 2020<\/strong>,\u00a0<strong><em>Genome Med 2020<\/em><\/strong>,\u00a0<strong><em>Genome Med 2021<\/em><\/strong>): to ensure that we&#8217;re advancing precision medicine for all.\u00a0<\/p>\n<\/blockquote>\n<blockquote>\n<p>We linked the identified mutations to likely treatment responses to targeted or immuno-therapy (<strong><em>Cell Rep Med 2021<\/em><\/strong>,\u00a0<strong><em>Cancers 2021<\/em><\/strong><em>,\u00a0<strong>Cell Reports 2021<\/strong><\/em>).<\/p>\n<\/blockquote>\n<blockquote>\n<p>To further bridge the gaps between genetics and treatments, we integrated proteomics data to validate genomic findings and identify new drug targets (<strong>Nat Comm 2017<\/strong>, <em><strong>Front Onc 2022<\/strong><\/em>).<\/p>\n<\/blockquote>\n<blockquote>\n<p>To decode downstream impacts of genetic variants, we built multi-omics software (<strong>MCP 2019<\/strong>,\u00a0<strong>Nat Comm 2021<\/strong><em>,\u00a0<strong>PSB 2021<\/strong><\/em>,\u00a0<strong><em>Comm Bio 2021<\/em><\/strong>) and publicly shared all codes.\u00a0<\/p>\n<\/blockquote>\n<p>PI Huang\u2019s\u00a0<strong>first\/co-first author research article: (bold); 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header_5_text_shadow_blur_strength_tablet=&#8221;1px&#8221; header_6_text_shadow_horizontal_length=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_horizontal_length_tablet=&#8221;0px&#8221; header_6_text_shadow_vertical_length=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_vertical_length_tablet=&#8221;0px&#8221; header_6_text_shadow_blur_strength=&#8221;header_6_text_shadow_style,%91object Object%93&#8243; header_6_text_shadow_blur_strength_tablet=&#8221;1px&#8221; box_shadow_horizontal_tablet=&#8221;0px&#8221; box_shadow_vertical_tablet=&#8221;0px&#8221; box_shadow_blur_tablet=&#8221;40px&#8221; box_shadow_spread_tablet=&#8221;0px&#8221; vertical_offset_tablet=&#8221;0&#8243; horizontal_offset_tablet=&#8221;0&#8243; z_index_tablet=&#8221;0&#8243;]<\/p>\n<h3><strong>What\u2019s missing, and what we are working on?\u00a0<\/strong><\/h3>\n<blockquote>\n<p>To predict disease risk or treatment, the current precision medicine paradigm often relies on single genetic mutations\/markers, thus disregarding much of the useful genomic information. Using national\/Mount Sinai biobank-scale genomic cohorts, we are actively developing <strong>Machine-Learning (ML) models that can more accurately predict disease risks and treatments using the full genome profile, with a focus on incorporating rare and structural variants (SV) in diverse populations<\/strong>.<\/p>\n<\/blockquote>\n<blockquote>\n<p>With 3 billion base pairs of DNA in a genome, it is difficult to identify critical genetic variants in complex diseases. We have effectively prioritized variants by <strong>resolving their downstream consequences on the transcriptome, proteome, and structures in cellular, spatial, and longitudinal resolution, with strong interests in protein targets directly related to functions and druggability<\/strong>.<\/p>\n<\/blockquote>\n<blockquote>\n<p>While genes identified from large-scale genomic cohorts can enrich for drug targets, most would still fail in pre-clinical development or clinical trials. We have developed methods to <strong>triage the target gene space by integrating multi-omics\u2014in particular those from reverse genetics screens\u2014thus achieving 10X improvement in pinpointing druggable genes<\/strong>.<\/p>\n<\/blockquote>\n<h3><strong>Acknowledgment<\/strong><\/h3>\n<p>We dedicate our work to study participants, patients, and their family. We thank the health workers at ISMMS and all institutions. 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Flaticon.<\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p><div class=\"et_pb_row et_pb_row_0 et_pb_row_empty\">\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t<\/div> What\u2019s Our Vision? Give us your genome, and we will accurately predict your disease risks and drug targets\u2014so you can benefit from personalized diagnostics, prevention, and treatment. <div class=\"et_pb_row et_pb_row_1 et_pb_row_empty\">\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t\t\n\t\t\t<\/div> How do we get there?\u00a0Here are selected examples of the scientific research done by our team:\u00a0We identified common risk variants in Alzheimer\u2019s disease (Nat Neuro 2017) [&hellip;]<\/p>\n","protected":false},"author":300,"featured_media":0,"parent":0,"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":""},"class_list":["post-747","page","type-page","status-publish","hentry"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/pages\/747","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/users\/300"}],"replies":[{"embeddable":true,"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/comments?post=747"}],"version-history":[{"count":29,"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/pages\/747\/revisions"}],"predecessor-version":[{"id":826,"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/pages\/747\/revisions\/826"}],"wp:attachment":[{"href":"https:\/\/labs.icahn.mssm.edu\/kuanhuanglab\/wp-json\/wp\/v2\/media?parent=747"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}