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Single-Cell Sequencing and Bulk Sequencing Bioinformatics Approaches

Dr. Elamathi Natarajan, Assistant Professor, Department of Bionformatics, Kalinga University

 

Genome understanding at advanced level:

In the advent of high-throughput sequencing technologies revolution  the intricacies of cellular process and genetic variation mysteries can be revealed. Out of various types of sequencing techniques, single-cell and bulk sequencing act as a powerful tools to understand the biological system complexities with different scales. In this article the significant bioinformatics approaches of single cell and bulk genome sequencing techniques are explored.

Single-Cell Sequencing and its applications:

One of the ground breaking technique emerged is a single-cell sequencing  technique which identify and have the ability to analyze the cellular heterogeneity, genetic material, developmental trajectories and disease mechanism of individual cells.  Granular view of cellular diversity within a population is exhibited through single-cell sequencing.  In complex biological system or heterogeneous tissues, single-cell sequencing  approach is considered as valuable and it is in practice recently. The numerous application of single-cell sequencing  in multiple fields which include cancer research, immunology, neuroscience and developmental biology. Genome, Transcriptome and epigenome either of this profile of individual cells in order to characterize cell interaction, identify rare cell population, delineate cell differentiation trajectories and dissect the cell disease state molecular mechanisms.  Advanced personalized medicine is facilitated by single- cell sequencing to identify the therapeutic targets and specific disease based biomarkers at single cell level.

Single-Cell Sequencing Data Analysis:

Challenges such as noise, inherent sparsity and high-dimensional nature of data  which analyzing single-cell sequencing data. The steps of  Bioinformatics pipelines for single-cell analysis  is mentioned below as follows. data preprocessing, quality control, dimensionality reduction, clustering, differential expression analysis and trajectory inference. From the single data sets to extract meaningful biological insights through data analysis approach.

 

Bulk Sequencing, analysis and its applications:

Bulk sequencing is an alternative  to single-cell sequencing approach. Wherein from population of cells DNA or RNA extracted  in order  to provide  genomics or transcriptomics landscape average representation within the sample. Bulk sequencing is cost effective and provide cornerstone of  indispensable Genomic research by doing analysis at population level of   Common Genetic variation, gene expression patterns and  genome-wide Epigenetics  modifications in various experimental conditions or disease states. Bulk sequencing data analysis include read alignment, variant calling, differential expression analysis, pathway enrichment analysis, and functional annotation.

 Conclusion:

To conclude both single-cell sequencing and bulk sequencing can be integrated  with in-silico approaches act as a novel tool to reveal mysteries of cell and genome mechanisms. Simultaneously  these techniques helps us to understand the biological systems complexity and advancing genome  constitute powerful tools for deciphering the complexities of biological systems and advancing Genomic understanding genome.

References:

  1. Lun, A. T., McCarthy, D. J., & Marioni, J. C. (2016). A step-by-step workflow for low-level analysis of single-cell RNA-seq data with Bioconductor. F1000Research, 5, 2122.
  2. McCarthy, D. J., Campbell, K. R., Lun, A. T., & Wills, Q. F. (2017). Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in R. Bioinformatics, 33(8), 1179–1186.
  3. Butler, A., Hoffman, P., Smibert, P., Papalexi, E., & Satija, R. (2018). Integrating single-cell transcriptomics data across different conditions, technologies, and species. Nature Biotechnology, 36(5), 411–420.
  4. Kiselev, V. Y., Kirschner, K., Schaub, M. T., Andrews, T., Yiu, A., Chandra, T., & Hemberg, M. (2017). SC3: consensus clustering of single-cell RNA-seq data. Nature Methods, 14(5), 483–486.
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  6. Wolf, F. A., Angerer, P., & Theis, F. J. (2018). SCANPY: large-scale single-cell gene expression data analysis. Genome Biology, 19(1), 15.
  7. Langmead, B., Trapnell, C., Pop, M., & Salzberg, S. L. (2009). Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biology, 10(3), R25.
  8. Li, H., & Durbin, R. (2009). Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25(14), 1754–1760.

 

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