Abstract Barcoding technology has greatly improved the throughput of cells and genes detected in single‐cell RNA sequencing (scRNA‐seq) studies. Recently, increasing studies have paid more attention to the use of this technology to increase the throughput of samples, as it has greatly reduced the processing time, technical batch effects, and library preparation costs, and lowered the per‐sample cost. In this review, the various DNA‐based barcoding methods for sample multiplexing are focused on, specifically, on the four major barcoding strategies. A detailed comparison of the barcoding methods is also presented, focusing on aspects such as sample/cell throughput and gene detection, and guidelines for choosing the most appropriate barcoding ...
International audienceMultiplexed single-cell RNA-sequencing (scRNA-seq) enables investigating sever...
This record contains raw data related to the article “Design of novel multiplex MinION sequencing wo...
Here we demonstrate a method for unbiased multiplexed deep sequencing of RNA and DNA libraries using...
Abstract Sample multiplexing facilitates single‐cell sequencing by reducing costs, revealing subtle ...
Abstract Background The multiplexing becomes the major limitation of the next-generation sequencing ...
The need to reduce per sample cost of RNA-seq profiling for scalable data generation has led to the ...
Cellular biology has traditionally relied upon simple, low-dimensional single-cell measurements (e.g...
We describe a highly sensitive, quantitative, and inexpensive technique for targeted sequencing of t...
The need to reduce per sample cost of RNA-seq profiling for scalable data generation has led to the ...
High-throughput single-cell assays increasingly require special consideration in experimental design...
Next-generation sequencing has proven an ex-tremely effective technology for molecular counting appl...
Background Multiplexing of samples in single-cell RNA-seq studies allows a significant reduction of ...
One powerfull tool in understanding how genetic variations can lead to changes in gene expression ac...
We describe a universal sample multiplexing method for single-cell RNA sequencing in which fixed cel...
This directory contains sequencing data in fastq format for three scRNA-seq experiments found in Geh...
International audienceMultiplexed single-cell RNA-sequencing (scRNA-seq) enables investigating sever...
This record contains raw data related to the article “Design of novel multiplex MinION sequencing wo...
Here we demonstrate a method for unbiased multiplexed deep sequencing of RNA and DNA libraries using...
Abstract Sample multiplexing facilitates single‐cell sequencing by reducing costs, revealing subtle ...
Abstract Background The multiplexing becomes the major limitation of the next-generation sequencing ...
The need to reduce per sample cost of RNA-seq profiling for scalable data generation has led to the ...
Cellular biology has traditionally relied upon simple, low-dimensional single-cell measurements (e.g...
We describe a highly sensitive, quantitative, and inexpensive technique for targeted sequencing of t...
The need to reduce per sample cost of RNA-seq profiling for scalable data generation has led to the ...
High-throughput single-cell assays increasingly require special consideration in experimental design...
Next-generation sequencing has proven an ex-tremely effective technology for molecular counting appl...
Background Multiplexing of samples in single-cell RNA-seq studies allows a significant reduction of ...
One powerfull tool in understanding how genetic variations can lead to changes in gene expression ac...
We describe a universal sample multiplexing method for single-cell RNA sequencing in which fixed cel...
This directory contains sequencing data in fastq format for three scRNA-seq experiments found in Geh...
International audienceMultiplexed single-cell RNA-sequencing (scRNA-seq) enables investigating sever...
This record contains raw data related to the article “Design of novel multiplex MinION sequencing wo...
Here we demonstrate a method for unbiased multiplexed deep sequencing of RNA and DNA libraries using...