Transcriptomics: Open Access
Open Access

Abstract

Utilization of Next Generation Sequencing in the Identification of Long Non-Coding RNAs as Potential Players in Breast Cancer Prevention

Hudson ME

The advancement of new advances, for example, Next Generation equencing (NGS), and techniques to improve the capacities of this innovation has been an unrest for the investigation of genomics and transcriptomics. NGS opens entryways for progress in an assortment of natural fields, including biomedical examination. NGS permits the sequencing of the entire genome and transcriptome in a gigantic scope, available cost, and it isn't restricted to past information. Genome sequencing has been applied for the improvement of an assortment of research zones, for example, portrayal of antiquated genomes , sequencing of various species , hazard evaluation of hereditary sicknesses , sub-atomic analysis of different sicknesses including malignant growth among other, prompting a street for customized medication. With NGS, definite investigations of the transcriptome have been made conceivable. Definite data about courier RNA, yet in addition ribosomal RNA, move RNA, little RNAs are presently available. Due to the way that this innovation needs no past information about the frameworks being contemplated contrasted with other high-throughput innovations (for example oligo-microarrays), NGS takes into account novel records to be found. Accordingly, elective joining, novel microRNAs, and non-coding districts which produce long non-coding RNAs (lncRNAs) would now be able to be investigated.

Published Date: 2021-02-21; Received Date: 2021-02-17