{"id":23829,"date":"2023-04-11T12:46:58","date_gmt":"2023-04-11T16:46:58","guid":{"rendered":"https:\/\/genomequebec.wp.vortexdev.com\/?post_type=service&#038;p=23829"},"modified":"2023-05-23T16:49:07","modified_gmt":"2023-05-23T20:49:07","slug":"articles","status":"publish","type":"service","link":"https:\/\/genomequebec.wp.vortexdev.com\/en\/technological-services\/centre-dexpertise-et-de-services-2\/articles\/","title":{"rendered":"Articles"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">Technology Applications<\/h2>\n\n\n\n<p><strong>WGS (resequencing, de novo sequencing)<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Pavy, N., Lamothe, M., Pelgas, B., Gagnon, F., Birol, I., Bohlmann, J., &#8230; Bousquet, J. (2017). A high resolution reference genetic map positioning 8.8K genes for the conifer white spruce: Structural genomics implications and correspondence with physical distance.&nbsp;<em>The Plant Journal: For Cell and Molecular Biology<\/em>.&nbsp;<a href=\"https:\/\/doi.org\/10.1111\/tpj.13478\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1111\/tpj.13478<\/a><\/li>\n\n\n\n<li>Low-Kam, C., Rhainds, D., Lo, K. S., Provost, S., Mongrain, I., Dubois, A., &#8230; Lettre, G. (2016). Whole-genome sequencing in French Canadians from Quebec. <em>Human Genetics, 135<\/em>(11), 1213-1221. <a href=\"https:\/\/doi.org\/10.1007\/s00439-016-1702-6\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1007\/s00439-016-1702-6<\/a><\/li>\n\n\n\n<li>Charron G, Marsit S, H\u00e9nault M, Martin H, Landry CR. Spontaneous whole-genome duplication restores fertility in interspecific hybrids. Nat Commun. 2019;10(1):4126. Published 2019 Sep 11. <a href=\"https:\/\/www.nature.com\/articles\/s41467-019-12041-8\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/www.nature.com\/articles\/s41467-019-12041-8<\/a><\/li>\n\n\n\n<li>Hagen IJ, Lien S, Billing AM, et al. A genome-wide linkage map for the house sparrow (Passer domesticus) provides insights into the evolutionary history of the avian genome. Mol Ecol Resour. 2020;20(2):544-559. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1111\/1755-0998.13134\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1111\/1755-0998.13134<\/a><\/li>\n\n\n\n<li>H\u00fcbner S, Bercovich N, Todesco M, et al. Sunflower pan-genome analysis shows that hybridization altered gene content and disease resistance. Nat Plants. 2019;5(1):54-62. <a rel=\"noreferrer noopener\" href=\"https:\/\/www.nature.com\/articles\/s41477-018-0329-0\" target=\"_blank\">https:\/\/www.nature.com\/articles\/s41477-018-0329-0<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>RNA Analysis (RNA Seq, Microarrays)<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Lopez, J. P., Fiori, L. M., Cruceanu, C., Lin, R., Labonte, B., Cates, H. M., \u2026 Turecki, G. (2017). MicroRNAs 146a\/b-5 and 425-3p and 24-3p are markers of antidepressant response and regulate MAPK\/Wnt-system genes. Nature Communications, 8, 15497. <a href=\"https:\/\/doi.org\/10.1038\/ncomms15497\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/ncomms15497<\/a><\/li>\n\n\n\n<li>Khater, F., Lajoie, M., Langlois, S., Healy, J., Cellot, S., Richer, C., &#8230; Sinnett, D. (2017). KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemia. <em>Blood<\/em>, blood-2016-10-744219.<a href=\"https:\/\/doi.org\/10.1182\/blood-2016-10-744219\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1182\/blood-2016-10-744219<\/a><\/li>\n\n\n\n<li>Liu, Y., Zhou, J., &amp; White, K. P. (2014). RNA-seq differential expression studies: more sequence or more replication? <em>Bioinformatics, 30<\/em>(3), 301-304.<a href=\"https:\/\/doi.org\/10.1093\/bioinformatics\/btt688\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1093\/bioinformatics\/btt68<\/a><\/li>\n\n\n\n<li>Couturier CP, Ayyadhury S, Le PU, et al. Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy. Nat Commun. 2020;11(1):3406. Published 2020 Jul 8. <a href=\"https:\/\/www.nature.com\/articles\/s41467-020-17186-5\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/www.nature.com\/articles\/s41467-020-17186-5<\/a><\/li>\n\n\n\n<li>Xue Y, Zhu X, Meehan B, et al. SMARCB1 loss induces druggable cyclin D1 deficiency via upregulation of MIR17HG in atypical teratoid rhabdoid tumors [published online ahead of print, 2020 Jun 19]. J Pathol. 2020;10.1002\/path.5493.<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/path.5493\" target=\"_blank\" rel=\"noopener\"> https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/path.5493<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>Targeted Sequencing (Exome Seq, DNA\/RNA captures, amplicons)<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Morin, A., Kwan, T., Ge, B., Letourneau, L., Ban, M., Tandre, K., &#8230; Pastinen, T. (2016). Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells. <em>BMC Medical Genomics, 9<\/em>(1), 59. <a href=\"https:\/\/doi.org\/10.1186\/s12920-016-0220-7\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1186\/s12920-016-0220-7<\/a><\/li>\n\n\n\n<li>Carrot-Zhang, J., &amp; Majewski, J. (2016). LoLoPicker: Detecting Low Allelic-Fraction Variants in Low-Quality Cancer Samples from Whole-exome Sequencing Data. <em>bioRxiv<\/em>, 43612. <a href=\"https:\/\/doi.org\/10.1101\/043612\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1101\/043612<\/a><\/li>\n\n\n\n<li>Ejaz, R., Qin, W., Huang, L., Blaser, S., Tetreault, M., Hartley, T., &#8230; Carter, M. T. (2016). Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation. <em>American Journal of Medical Genetics. Part A, 170A<\/em>(4), 1070-5.<a href=\"https:\/\/doi.org\/10.1002\/ajmg.a.37541\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1002\/ajmg.a.37541<\/a><\/li>\n\n\n\n<li>Choquet, K., T\u00e9treault, M., Yang, S., La Piana, R., Dicaire, M.-J., Vanstone, M. R., &#8230; Brais, B. (2016). SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases. <em>European Journal of Human Genetics : EJHG, 24<\/em>(7), 1016-21. <a href=\"https:\/\/doi.org\/10.1038\/ejhg.2015.240\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/ejhg.2015.240<\/a><\/li>\n\n\n\n<li>Nicolas, G., Wallon, D., Charbonnier, C., Quenez, O., Rousseau, S., Richard, A.-C., &#8230; Hannequin, D. (2016). Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons. <em>European Journal of Human Genetics, 24<\/em>(5), 710-716. <a href=\"https:\/\/doi.org\/10.1038\/ejhg.2015.173\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/ejhg.2015.173<\/a><\/li>\n\n\n\n<li>de Kock, L., Wang, Y. C., Revil, T., Badescu, D., Rivera, B., Sabbaghian, N., &#8230; Foulkes, W. D. (2016). High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome. <em>Journal of Medical Genetics, 53<\/em>(1), 43-52.<a href=\"https:\/\/doi.org\/10.1136\/jmedgenet-2015-103428\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1136\/jmedgenet-2015-103428<\/a><\/li>\n\n\n\n<li>Nikbakht, H., Panditharatna, E., Mikael, L. G., Li, R., Gayden, T., Osmond, M., &#8230; Nazarian, J. (2016). Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma. <em>Nature Communications, 7<\/em>, 11185.<a href=\"https:\/\/doi.org\/10.1038\/ncomms11185\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/ncomms11185<\/a><\/li>\n\n\n\n<li>Rivera, B., Gayden, T., Carrot-Zhang, J., Nadaf, J., Boshari, T., Faury, D., &#8230; Majewski, J. (2016). Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors. <em>Acta Neuropathologica, 131<\/em>(6), 847-863. <a href=\"https:\/\/doi.org\/10.1007\/s00401-016-1549-x\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1007\/s00401-016-1549-x<\/a><\/li>\n\n\n\n<li>Armour, C. M., Smith, A., Hartley, T., Chardon, J. W., Sawyer, S., Schwartzentruber, J., &#8230; Boycott, K. M. (2016). Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events. <em>American Journal of Medical Genetics Part A, 170<\/em>(7), 1820-1825.<a href=\"https:\/\/doi.org\/10.1002\/ajmg.a.37684\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1002\/ajmg.a.37684<\/a><\/li>\n\n\n\n<li>McCluggage WG, Chong AL, de Kock L, Foulkes WD. Somatic tumour testing establishes that bilateral DICER1-associated ovarian Sertoli-Leydig cell tumours represent independent primary neoplasms [published online ahead of print, 2020 Apr 24]. Histopathology. 2020;10.<a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1111\/his.14123\" target=\"_blank\">https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1111\/his.14123<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>PacBio Sequencing<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Xiong, J., D\u00e9raspe, M., Iqbal, N., Ma, J., Jamieson, F. B., Wasserscheid, J., &#8230; Roy, P. H. (2016). Genome and Plasmid Analysis of blaIMP-4-Carrying Citrobacter freundii B38. <em>Antimicrobial Agents and Chemotherapy, 60<\/em>(11), 6719-6725. <a href=\"https:\/\/doi.org\/10.1128\/AAC.00588-16\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1128\/AAC.00588-16<\/a><\/li>\n\n\n\n<li>Ricker, N., Shen, S. Y., Goordial, J., Jin, S., &amp; Fulthorpe, R. R. (2016). PacBio SMRT assembly of a complex multi-replicon genome reveals chlorocatechol degradative operon in a region of genome plasticity. <em>Gene, 586<\/em>(2), 239-247. <a href=\"https:\/\/doi.org\/10.1016\/j.gene.2016.04.018\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1016\/j.gene.2016.04.018<\/a><\/li>\n\n\n\n<li>Bromfield ESP, Cloutier S, Nguyen HDT. Description and complete genome sequence of Bradyrhizobium amphicarpaeae sp. nov., harbouring photosystem and nitrogen-fixation genes. Int J Syst Evol Microbiol. 2019;69(9):2841-2848. <a rel=\"noreferrer noopener\" href=\"https:\/\/www.microbiologyresearch.org\/content\/journal\/ijsem\/10.1099\/ijsem.0.003569\" target=\"_blank\">https:\/\/www.microbiologyresearch.org\/content\/journal\/ijsem\/10.1099\/ijsem.0.003569<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>Epigenetics (Methyl Seq, biopuces)<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Chen, G. G., Gross, J. A., Lutz, P.-E., Vaillancourt, K., Maussion, G., Bramoulle, A., &#8230; Ernst, C. (2017). Medium throughput bisulfite sequencing for accurate detection of 5-methylcytosine and 5-hydroxymethylcytosine. <em>BMC Genomics, 18<\/em>(1), 96. <a href=\"https:\/\/doi.org\/10.1186\/s12864-017-3489-9\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1186\/s12864-017-3489-9<\/a><\/li>\n\n\n\n<li>Chen, L., Ge, B., Casale, F. P., Vasquez, L., Kwan, T., Garrido-Mart\u00c3\u00adn, D., &#8230; Soranzo, N. (2016). Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells. <em>Cell, 167<\/em>(5), 1398-1414.e24.<a href=\"https:\/\/doi.org\/10.1016\/j.cell.2016.10.026\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1016\/j.cell.2016.10.026<\/a><\/li>\n\n\n\n<li>Ho, V., Ashbury, J. E., Taylor, S., Vanner, S., &amp; King, W. D. (2016). Quantification of gene-specific methylation of DNMT3B and MTHFR using sequenom EpiTYPER\u00c2\u00ae. <em>Data in Brief, 6<\/em>, 39-46. <a href=\"https:\/\/doi.org\/10.1016\/j.dib.2015.11.039\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1016\/j.dib.2015.11.039<\/a><\/li>\n\n\n\n<li>Sarnowski, C., Laprise, C., Malerba, G., Moffatt, M. F., Dizier, M.-H., Morin, A., &#8230; Bouzigon, E. (2016). DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis.<em>Journal of Allergy and Clinical Immunology, 138<\/em>(3), 748-753. https:\/\/doi.org\/10.1016\/j.jaci.2015.12.1341 <a href=\"https:\/\/doi.org\/10.1111\/tpj.13478\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1111\/tpj.13478<\/a><\/li>\n\n\n\n<li>Allum, F., Shao, X., Gu\u00e9nard, F., Simon, M.-M., Busche, S., Caron, M., &#8230; Grundberg, E. (2015). Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants. <em>Nature Communications, 6<\/em>, 7211. <a href=\"https:\/\/doi.org\/10.1038\/ncomms8211\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/ncomms8211<\/a><\/li>\n\n\n\n<li>Busche, S., Shao, X., Caron, M., Kwan, T., Allum, F., Cheung, W. A., &#8230; Grundberg, E. (2015). Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation. <em>Genome Biology, 16<\/em>(1), 290. <a href=\"https:\/\/doi.org\/10.1186\/s13059-015-0856-1\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1186\/s13059-015-0856-1<\/a><\/li>\n\n\n\n<li>El-Zein M, Cheishvili D, Gotlieb W, et al. Genome-wide DNA methylation profiling identifies two novel genes in cervical neoplasia [published online ahead of print, 2020 Jan 25]. Int J Cancer. 2020;10.1002\/ijc.32880. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ijc.32880\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ijc.32880<\/a><\/li>\n\n\n\n<li>Lu T, Klein KO, Colmegna I, Lora M, Greenwood CMT, Hudson M. Whole-genome bisulfite sequencing in systemic sclerosis provides novel targets to understand disease pathogenesis. BMC Med Genomics. 2019;12(1):144. Published 2019 Oct 24. <a href=\"https:\/\/bmcmedgenomics.biomedcentral.com\/articles\/10.1186\/s12920-019-0602-8\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/bmcmedgenomics.biomedcentral.com\/articles\/10.1186\/s12920-019-0602-8<\/a><\/li>\n\n\n\n<li>Barr\u00eda A, Christensen KA, Yoshida G, et al. Whole Genome Linkage Disequilibrium and Effective Population Size in a Coho Salmon (Oncorhynchus kisutch) Breeding Population Using a High-Density SNP Array. Front Genet. 2019;10:498. Published 2019 May 22. <a rel=\"noreferrer noopener\" href=\"https:\/\/www.frontiersin.org\/articles\/396472\" target=\"_blank\">https:\/\/www.frontiersin.org\/articles\/396472<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>Genotyping (Microarrays, iPLEX Gold, TaqMan)<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Pavy, N., Gagnon, F., Desch\u00c3\u00aanes, A., Boyle, B., Beaulieu, J., &amp; Bousquet, J. (2016). Development of highly reliable in silico SNP resource and genotyping assay from exome capture and sequencing: an example from black spruce ( <em>Picea mariana<\/em> ). <em>Molecular Ecology Resources, 16<\/em>(2), 588-598.<a href=\"https:\/\/doi.org\/10.1111\/1755-0998.12468\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1111\/1755-0998.12468<\/a><\/li>\n\n\n\n<li>Gagn\u00e9 V, Aubry-Morin A, Plesa M, et al. Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients. Pharmacogenomics. 2019;20(17):1189-1197. <a rel=\"noreferrer noopener\" href=\"https:\/\/www.futuremedicine.com\/doi\/10.2217\/pgs-2019-0087\" target=\"_blank\">https:\/\/www.futuremedicine.com\/doi\/10.2217\/pgs-2019-0087<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>ChIP Seq<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Hocking, T. D., Goerner-Potvin, P., Morin, A., Shao, X., Pastinen, T., &amp; Bourque, G. (2016). Optimizing ChIP-seq peak detectors using visual labels and supervised machine learning. <em>Bioinformatics (Oxford, England), 33<\/em>(4), 491-499.<a href=\"https:\/\/doi.org\/10.1093\/bioinformatics\/btw672\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1093\/bioinformatics\/btw672<\/a><\/li>\n\n\n\n<li>Furey, T. S. (2012). ChIP-seq and beyond: new and improved methodologies to detect and characterize protein-DNA interactions. <em>Nature Reviews Genetics, 13<\/em>(12), 840-852. <a href=\"https:\/\/doi.org\/10.1038\/nrg3306\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/nrg3306<\/a><\/li>\n\n\n\n<li>Kidder, B. L., Hu, G., &amp; Zhao, K. (2011). ChIP-Seq: technical considerations for obtaining high-quality data. <em>Nature Immunology, 12<\/em>(10), 918-922.<a href=\"https:\/\/doi.org\/10.1038\/ni.2117\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/doi.org\/10.1038\/ni.2117<\/a><\/li>\n\n\n\n<li>Behl S, Hamel N, de Ladurantaye M, et al. Founder BRCA1\/BRCA2\/PALB2 pathogenic variants in French-Canadian breast cancer cases and controls. Sci Rep. 2020;10(1):6491. Published 2020 Apr 16. <a rel=\"noreferrer noopener\" href=\"https:\/\/www.nature.com\/articles\/s41598-020-63100-w\" target=\"_blank\">https:\/\/www.nature.com\/articles\/s41598-020-63100-w<\/a><\/li>\n<\/ul>\n\n\n\n<p><strong>Metagenomics and Metabarcoding<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Minerbi A, Gonzalez E, Brereton NJB, et al. Altered microbiome composition in individuals with fibromyalgia. Pain. 2019;160(11):2589-2602. <a rel=\"noreferrer noopener\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/31219947\/\" target=\"_blank\">https:\/\/pubmed.ncbi.nlm.nih.gov\/31219947\/<\/a><\/li>\n<\/ul>\n\n\n\n<div class=\"wp-block-buttons is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link wp-element-button\" href=\"https:\/\/cesgq.com\/articles#publications-intro\" target=\"_blank\" rel=\"noopener\">BACK TO THE SUMMARY<\/a><\/div>\n<\/div>\n","protected":false},"featured_media":0,"parent":26647,"menu_order":0,"template":"","class_list":["post-23829","service","type-service","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/genomequebec.wp.vortexdev.com\/en\/wp-json\/wp\/v2\/service\/23829","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/genomequebec.wp.vortexdev.com\/en\/wp-json\/wp\/v2\/service"}],"about":[{"href":"https:\/\/genomequebec.wp.vortexdev.com\/en\/wp-json\/wp\/v2\/types\/service"}],"up":[{"embeddable":true,"href":"https:\/\/genomequebec.wp.vortexdev.com\/en\/wp-json\/wp\/v2\/service\/26647"}],"wp:attachment":[{"href":"https:\/\/genomequebec.wp.vortexdev.com\/en\/wp-json\/wp\/v2\/media?parent=23829"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}