We are excited to announce a new version of Enlis Genome Research!\u00c2\u00a0 Our customers are having fantastic success in using our software to go quickly from data to discovery.<\/p>\n
<\/p>\n
Version 1.7 highlights: We are excited to announce a new version of Enlis Genome Research!\u00c2\u00a0 Our customers are having fantastic success in using our software to go quickly from data to discovery. Version 1.7 highlights: – New Clinical Variation Annotations This release includes over 120,000 variant to phenotype classifications.\u00c2\u00a0 Built-in filters allow you to quickly identify what […]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-60","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/posts\/60","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/comments?post=60"}],"version-history":[{"count":0,"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/posts\/60\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/media?parent=60"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/categories?post=60"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.enlis.com\/blog\/wp-json\/wp\/v2\/tags?post=60"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
\n– New Clinical Variation Annotations
\nThis release includes over 120,000 variant to phenotype classifications.\u00c2\u00a0 Built-in filters allow you to quickly identify what is already known about the genomes you are studying.
\n– New Citation Annotations
\nPublications that support a variant to phenotype classification are listed on the position pages.\u00c2\u00a0 Link to Pubmed, or if the associated PDF is freely available, link directly to the PDF.
\n– New Homozygous Regions Detector tool
\nFind regions of the genome with “runs” of consecutive homozygous variants.\u00c2\u00a0 For rare disease analysis, these regions may indicate a consanguineous union, and provide a starting point for finding recessive disease.\u00c2\u00a0 In tumor samples, these regions may indicate loss of heterozygosity.
\n– Genome Import: Significant speed improvements
\nImport of VCF, Complete Genomics data, and other variation files is 30% – 600% faster depending on import size.
\nNumerous other bugs fixes and features – full release notes can be found here: http:\/\/files.enlisgenomics.com\/ReleaseNotes.pdf <\/a>
\nGetting started is easy, see our new “Getting Started” video here: https:\/\/www.enlis.com\/video.html<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"