Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods

October 3, 2019 Leave a comment 2,080 Views

Standard RNAseq methods using bulk RNA and recent single-cell RNAseq methods use DNA barcodes to identify samples and cells, and the barcoded cDNAs are pooled into a library pool before high throughput sequencing. In cases of single-cell and low-input RNAseq ...

RNA-Seq Blog Transcriptome Research & Industry News

Tag Archives: Library bias correction

Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods

Researchers construct a high-resolution single-nucleus RNA sequencing (snRNA-seq) analysis of gene expression changes across all brain cell

Zebrahub – a single-embryo single-cell RNA sequencing atlas of zebrafish development

Post-doc position available – RNA Accelerator Inflammation and Immunology

BEETLE ATLAS – a definitive, tissue-specific transcriptomic resource based on RNA-Seq data for the Tribolium community

ElasticBLAST – accelerating sequence search via cloud computing

TileDB launches cross-language access to single-cell data

Researchers have developed an instrument-free single-cell RNA sequencing using a reversible hydrogel for cell-specific barcoding