[HTML][HTML] Obstacles to detecting isoforms using full-length scRNA-seq data

J Westoby, P Artemov, M Hemberg, A Ferguson-Smith - Genome Biology, 2020 - Springer
Background Early single-cell RNA-seq (scRNA-seq) studies suggested that it was unusual
to see more than one isoform being produced from a gene in a single cell, even when …

[HTML][HTML] Single-cell RNAseq for the study of isoforms—how is that possible?

Á Arzalluz-Luque, A Conesa - Genome biology, 2018 - Springer
Single-cell RNAseq and alternative splicing studies have recently become two of the most
prominent applications of RNAseq. However, the combination of both is still challenging …

[HTML][HTML] Detecting differential alternative splicing events in scRNA-seq with or without Unique Molecular Identifiers

Y Hu, K Wang, M Li - PLoS computational biology, 2020 - journals.plos.org
The emergence of single-cell RNA-seq (scRNA-seq) technology has made it possible to
measure gene expression variations at cellular level. This breakthrough enables the …

[HTML][HTML] BRIE: transcriptome-wide splicing quantification in single cells

Y Huang, G Sanguinetti - Genome biology, 2017 - Springer
Single-cell RNA-seq (scRNA-seq) provides a comprehensive measurement of stochasticity
in transcription, but the limitations of the technology have prevented its application to dissect …

[HTML][HTML] Towards reliable isoform quantification using RNA-SEQ data

BE Howard, S Heber - BMC bioinformatics, 2010 - Springer
Background In eukaryotes, alternative splicing often generates multiple splice variants from
a single gene. Here weexplore the use of RNA sequencing (RNA-Seq) datasets to address …

[HTML][HTML] BRIE2: computational identification of splicing phenotypes from single-cell transcriptomic experiments

Y Huang, G Sanguinetti - Genome biology, 2021 - Springer
RNA splicing is an important driver of heterogeneity in single cells through the expression of
alternative transcripts and as a determinant of transcriptional kinetics. However, the intrinsic …

PrimerSeq: design and visualization of RT-PCR primers for alternative splicing using RNA-seq data

C Tokheim, JW Park, Y Xing - Genomics, Proteomics and …, 2014 - academic.oup.com
The vast majority of multi-exon genes in higher eukaryotes are alternatively spliced and
changes in alternative splicing (AS) can impact gene function or cause disease. High …

[HTML][HTML] KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data

GAT Sacomoto, J Kielbassa, R Chikhi, R Uricaru… - BMC …, 2012 - Springer
Background In this paper, we address the problem of identifying and quantifying
polymorphisms in RNA-seq data when no reference genome is available, without …

MAJIQ-SPEL: web-tool to interrogate classical and complex splicing variations from RNA-Seq data

CJ Green, MR Gazzara, Y Barash - Bioinformatics, 2018 - academic.oup.com
Analysis of RNA sequencing (RNA-Seq) data have highlighted the fact that most genes
undergo alternative splicing (AS) and that these patterns are tightly regulated. Many of these …

Robust detection of alternative splicing in a population of single cells

JD Welch, Y Hu, JF Prins - Nucleic acids research, 2016 - academic.oup.com
Single cell RNA-seq experiments provide valuable insight into cellular heterogeneity but
suffer from low coverage, 3′ bias and technical noise. These unique properties of single …