Overcome analytical bottlenecks in RNA-Seq experiments with limited number of replicates and low sequencing coverage

January 4, 2018 Leave a comment 4,308 Views

In current statistical methods for calling differentially expressed genes in RNA-Seq experiments, the assumption is that an adjusted observed gene count represents an unknown true gene count...

RNA-Seq Blog Transcriptome Research & Industry News

Tag Archives: Sequencing coverage

Overcome analytical bottlenecks in RNA-Seq experiments with limited number of replicates and low sequencing coverage

High-throughput droplet-based analysis of influenza A virus genetic reassortment by single-virus RNA sequencing

The way genes are switched on in one-cell embryos may resemble the trigger for cancer

scONE-seq – A single-cell multi-omics method enables simultaneous dissection of phenotype and genotype heterogeneity from frozen tumors

Phasik – inferring cell cycle phases from a partially temporal network of protein interactions

Single-cell transcriptomic profiling of Crohn’s disease reveals a detailed picture of inflammation in the gut

Gene expression model inference from snapshot RNA data using Bayesian non-parametrics

LeukemiaDB – a comprehensive human leukemia transcriptome database