{"version":"1.0","type":"rich","provider_name":"Acast","provider_url":"https://acast.com","height":250,"width":700,"html":"<iframe src=\"https://embed.acast.com/$/61a48e6defe03000141336e0/642e91c2ac6baa0011a7e7f5?\" frameBorder=\"0\" width=\"700\" height=\"250\"></iframe>","title":"Cancer whole transcriptome sequencing services","thumbnail_width":200,"thumbnail_height":200,"thumbnail_url":"https://open-images.acast.com/shows/undefined/1638174257576-b93102ad18d95cb412bbf011fb35a99e.jpeg?height=200","description":"<p><a href=\"https://www.creative-biolabs.com/suprecision/whole-transcriptome-sequencing-service-for-cancer.htm\" rel=\"noopener noreferrer\" target=\"_blank\">RNA-seq</a> is a revolutionary tool with better resolution and higher reproducibility that offers many advantages over the traditional microarray technologies. RNA-seq can be used to extend our knowledge of alternative splicing events, novel genes and transcripts, and fusion transcripts. RNA-seq can also help to understand molecular mechanisms and then it tells about signaling pathways which controls embryonic development. The transcriptome data give researchers a good place to start searching for a newly found gene's function.</p>","author_name":"Jerry Carter"}