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

January 4, 2018 Leave a comment 3,993 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...

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Tag Archives: Sequencing coverage

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

iDIRECT – disentangling direct from indirect relationships in association networks

small RNA sequencing suggests BPA exposure of the placenta could affect fetal brain development

A comprehensive comparison of supervised and unsupervised methods for cell type identification in single-cell RNA-seq

Using synthetic chromosome controls to evaluate the sequencing of difficult regions within the human genome

LMU researchers have developed a method to extract more information from RNA sequencing data

Long read sequencing reveals novel isoforms and insights into splicing regulation during cell state changes

Lucence’s LiquidHALLMARK Sequencing-based Liquid Biopsy Assay Expands to Include cfRNA