{"id":55,"date":"2019-10-31T15:03:23","date_gmt":"2019-10-31T15:03:23","guid":{"rendered":"https:\/\/www.embl.org\/groups\/korbel\/?page_id=55"},"modified":"2020-08-01T09:11:32","modified_gmt":"2020-08-01T09:11:32","slug":"services","status":"publish","type":"page","link":"https:\/\/www.embl.org\/groups\/korbel\/services\/","title":{"rendered":"Services"},"content":{"rendered":"\n<h3 class=\"wp-block-heading\">High-throughput sequencing<\/h3>\n\n\n\n<table class=\"wp-block-table is-style-stripes\"><tbody><tr><td><a href=\"http:\/\/www.korbel.embl.de\/CopySeq\/\">CopySeq<\/a><\/td><td>Discovery and copy-number genotyping of genomic structural variants<\/td><\/tr><tr><td><a href=\"https:\/\/github.com\/tobiasrausch\/delly\" target=\"_blank\" rel=\"noreferrer noopener\">DELLY<\/a><\/td><td>Integrated split-read and paired-end based structural variant discovery in massively parallel sequencing data<\/td><\/tr><tr><td><a href=\"http:\/\/www.korbel.embl.de\/PEMer\/\">PEMer<\/a><\/td><td>Discovery of genomic structural variants by high-throughput and massive paired-end mapping<\/td><\/tr><\/tbody><\/table>\n\n\n\n<h3 class=\"wp-block-heading\">Sequence Analysis<\/h3>\n\n\n\n<table class=\"wp-block-table\"><tbody><tr><td><a href=\"http:\/\/www.embl.de\/~korbel\/breakseq\/\">BreakSeq<\/a><\/td><td>Nucleotide-resolution genotyping of structural variants in personal genomics data<\/td><\/tr><\/tbody><\/table>\n\n\n\n<h3 class=\"wp-block-heading\">Miscellaneous<\/h3>\n\n\n\n<table class=\"wp-block-table is-style-stripes\"><tbody><tr><td><a href=\"http:\/\/tiling.mbb.yale.edu\/BreakPtr\/\">BreakPtr<\/a><\/td><td>Mapping copy-number variation with high-density oligonucleotide tiling arrays.<br><br><\/td><\/tr><tr><td><a href=\"http:\/\/www.korbel.embl.de\/PEMer\/\">PEMer<\/a><\/td><td>Discovery of genomic structural variants by high-throughput and massive paired-end mapping<\/td><\/tr><\/tbody><\/table>\n","protected":false},"excerpt":{"rendered":"<p>High-throughput sequencing CopySeq Discovery and copy-number genotyping of genomic structural variants DELLY Integrated split-read and paired-end based structural variant discovery in massively parallel sequencing data PEMer Discovery of genomic structural variants by high-throughput and massive&hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"template-with-sidebar.php","meta":{"_acf_changed":false,"footnotes":""},"embl_taxonomy":[],"class_list":["post-55","page","type-page","status-publish","hentry"],"acf":[],"embl_taxonomy_terms":[],"_links":{"self":[{"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/pages\/55","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/comments?post=55"}],"version-history":[{"count":3,"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/pages\/55\/revisions"}],"predecessor-version":[{"id":58,"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/pages\/55\/revisions\/58"}],"wp:attachment":[{"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/media?parent=55"}],"wp:term":[{"taxonomy":"embl_taxonomy","embeddable":true,"href":"https:\/\/www.embl.org\/groups\/korbel\/wp-json\/wp\/v2\/embl_taxonomy?post=55"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}