{"id":33149,"date":"2022-04-22T02:53:54","date_gmt":"2022-04-22T09:53:54","guid":{"rendered":"https:\/\/www.novogene.com\/us-en\/?post_type=resources&#038;p=33149"},"modified":"2022-05-05T19:38:46","modified_gmt":"2022-05-06T02:38:46","slug":"a-beginners-guide-to-dna-seq-bioinformatics-analysis","status":"publish","type":"resources","link":"https:\/\/www.novogene.com\/us-en\/resources\/event\/a-beginners-guide-to-dna-seq-bioinformatics-analysis\/","title":{"rendered":"A Beginner&#8217;s Guide to DNA-seq Bioinformatics Analysis"},"content":{"rendered":"<p><iframe loading=\"lazy\" width=\"560\" height=\"315\" src=\"https:\/\/www.youtube.com\/embed\/h3u7yfyIMEA\" title=\"YouTube video player\" frameborder=\"0\" allow=\"accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture\" allowfullscreen><\/iframe><\/p>\n<p>Webinar time: 21-Apr-2022 Updated time: 22-Apr-2022 Region: Europe<\/p>\n<p>Next generation sequencing (NGS) technologies enable ambitious large-scale genomic sequencing efforts. The detection of genetic variation is of major interest in various disciplines spanning from ecology and evolution research to inherited disease discovery and precision oncology.<\/p>\n<p>In this \u2018beginner\u2019s guide\u2019 webinar, our technical expert will discuss different analysis tools and pipelines used for variation identification (based on short- and long-read sequencing data) and outline advanced analysis options to help researchers fulfil their research needs.<\/p>\n<p>In this free beginner\u2019s guide webinar, you will learn about:<\/p>\n<p>* Commonly used variant calling pipelines for Illumina, PacBio and Nanopore data<br \/>\n* Advanced analysis approaches for disease and cancer studies<br \/>\n* Various data handling software and file formats<\/p>\n","protected":false},"featured_media":0,"parent":0,"template":"","yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v20.8 (Yoast SEO v20.8) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>A Beginner&#039;s Guide to DNA-seq Bioinformatics Analysis - Novogene<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.novogene.com\/us-en\/resources\/event\/a-beginners-guide-to-dna-seq-bioinformatics-analysis\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"A Beginner&#039;s Guide to DNA-seq Bioinformatics Analysis\" \/>\n<meta property=\"og:description\" content=\"Webinar time: 21-Apr-2022 Updated time: 22-Apr-2022 Region: Europe Next generation sequencing (NGS) technologies enable ambitious large-scale genomic sequencing efforts. The detection of genetic variation is of major interest in various disciplines spanning from ecology and evolution research to inherited disease discovery and precision oncology. 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