Misra, P and Jadhav, AR and Bapat, SA (2022) Single-cell sequencing: A cutting edge tool in molecular medical research. Medical Journal Armed Forces Journal India, 78. S7-S13.
Full text not available from this repository. (Request a copy)Abstract
The rapid development of advanced high throughput technologies and introduction of high resolution “omics” data through analysis of biological molecules has revamped medical research. Single-cell sequencing in recent years, is in fact revolutionising the field by providing a deeper, spatio-temporal analyses of individual cells within tissues and their relevance to disease. Like conventional sequencing, the single-cell approach deciphers the sequence of nucleotides in a given Deoxyribose Nucleic Acid (DNA), Ribose Nucleic Acid (RNA), Micro Ribose Nucleic Acid (miRNA), epigenetically modified DNA or chromatin DNA; however, the unit of analyses is changed to single cells rather than the entire tissue. Further, a large number of single cells analysed from a single tissue generate a unique holistic perception capturing all kinds of perturbations across different cells in the tissue that increases the precision of data. Inherently, execution of the technique generates a large amount of data, which is required to be processed in a specific manner followed by customised bioinformatic analysis to produce meaningful results. The most crucial role of single-cell sequencing technique is in elucidating the inter-cell genetic, epigenetic, transcriptomic and proteomic heterogeneity in health and disease. The current review presents a brief overview of this cutting-edge technology and its applications in medical research.
Item Type: | Article |
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Subjects: | Cancer Biology |
Depositing User: | Mr. Rameshwar Nema |
Date Deposited: | 20 Oct 2022 11:50 |
Last Modified: | 20 Oct 2022 11:50 |
URI: | http://nccs.sciencecentral.in/id/eprint/1210 |
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