Ultra-fast pseudo-alignment approaches are the tool of choice in transcript-level RNA sequencing (RNA-seq) analyses. Unfortunately, these methods couple the tasks of pseudo-alignment and transcript quantification. This coupling precludes the direct usage of pseudo-alignment to other expression analyses, including alternative splicing or differential gene expression analysis, without including a non-essential transcript quantification step.https://doi.org/10.1186/s12859-019-2947-
Motivation: RNA-seq techniques provide an unparalleled means for exploring a transcriptome with deep...
The advance of high-throughput sequencing technologies and their application on mRNA transcriptome s...
High-throughput mRNA sequencing (RNA-Seq) promises simultaneous transcript discovery and abundance e...
This is the supporting data and analysis scripts used for experiments in Yanagi paper. Background: ...
Analysis of differential alternative splicing from RNA-seq data is complicated by the fact that many...
The emergence of RNA-seq technology has made it possible to estimate isoform-specific gene expressio...
The emergence of RNA-seq technology has made it possible to estimate isoform-specific gene expressio...
RNA-sequencing has revolutionized biomedical research and, in particular, our ability to study gene ...
The advent of high throughput RNA-seq technology allows deep sampling of the transcriptome, making i...
Motivation: Genome alignment of reads is the first step of most genome analysis workflows. In the ca...
Motivation: RNA-Seq technique has been demonstrated as a revolutionary means for exploring transcrip...
Background: Massively parallel whole transcriptome sequencing, commonly referred as RNA-Seq, is quic...
Alternative splicing plays an essential role in many cellular processes and bears major relevance in...
We present a novel expectation-maximization algorithm for inference of alternative splicing isoform ...
Alternative splicing is critical for human gene expression regulation and plays an important role in...
Motivation: RNA-seq techniques provide an unparalleled means for exploring a transcriptome with deep...
The advance of high-throughput sequencing technologies and their application on mRNA transcriptome s...
High-throughput mRNA sequencing (RNA-Seq) promises simultaneous transcript discovery and abundance e...
This is the supporting data and analysis scripts used for experiments in Yanagi paper. Background: ...
Analysis of differential alternative splicing from RNA-seq data is complicated by the fact that many...
The emergence of RNA-seq technology has made it possible to estimate isoform-specific gene expressio...
The emergence of RNA-seq technology has made it possible to estimate isoform-specific gene expressio...
RNA-sequencing has revolutionized biomedical research and, in particular, our ability to study gene ...
The advent of high throughput RNA-seq technology allows deep sampling of the transcriptome, making i...
Motivation: Genome alignment of reads is the first step of most genome analysis workflows. In the ca...
Motivation: RNA-Seq technique has been demonstrated as a revolutionary means for exploring transcrip...
Background: Massively parallel whole transcriptome sequencing, commonly referred as RNA-Seq, is quic...
Alternative splicing plays an essential role in many cellular processes and bears major relevance in...
We present a novel expectation-maximization algorithm for inference of alternative splicing isoform ...
Alternative splicing is critical for human gene expression regulation and plays an important role in...
Motivation: RNA-seq techniques provide an unparalleled means for exploring a transcriptome with deep...
The advance of high-throughput sequencing technologies and their application on mRNA transcriptome s...
High-throughput mRNA sequencing (RNA-Seq) promises simultaneous transcript discovery and abundance e...