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Single-cell sequencing examines the nucleic acid sequence information from individual cells with optimized next-generation sequencing technologies, providing a higher resolution of cellular differences and a better understanding of the function of an individual cell in the context of its microenvironment. [1]
This single cell shows the process of the central dogma of molecular biology, which are all steps researchers are interested to quantify (DNA, RNA, and Protein).. In cell biology, single-cell analysis and subcellular analysis [1] refer to the study of genomics, transcriptomics, proteomics, metabolomics, and cell–cell interactions at the level of an individual cell, as opposed to more ...
Two methods for single-cell ATAC-seq [8]. ATAC-seq stands for Assay for Transposase-Accessible Chromatin with high throughput sequencing. [9] It is a technique used in molecular biology to identify accessible DNA regions, equivalent to DNase I hypersensitive sites. [9]
As a result of the aforementioned properties of single-cell transcriptomic data, batch correction methods developed for bulk sequencing data were observed to perform poorly. Consequently, researchers developed statistical methods to correct for batch effects that are robust to the properties of single-cell transcriptomic data to integrate data ...
The DNA sequencing is done on a chip that contains many ZMWs. Inside each ZMW, a single active DNA polymerase with a single molecule of single stranded DNA template is immobilized to the bottom through which light can penetrate and create a visualization chamber that allows monitoring of the activity of the DNA polymerase at a single molecule level.
The genome sequence of a single cell selected from a mixed population of cells can be determined using techniques of single cell genome sequencing. This has important advantages in environmental microbiology in cases where a single cell of a particular microorganism species can be isolated from a mixed population by microscopy on the basis of ...
A list of more than 100 different single cell sequencing (omics) methods have been published. [1] The large majority of methods are paired with short-read sequencing technologies, although some of them are compatible with long read sequencing.
paired-end PCR-free reads (successor of ALLPATHS-LG) Illumina (MiSeq or HiSeq 2500) [11] 2014 OS link: DNA Baser Sequence Assembler DNA sequence assembly with automatic end trimming & ambiguity correction. Includes a base caller. Sanger, Illumina Heracle BioSoft SRL 2018.09 C ($69) NA DNASTAR Lasergene Genomics