Transcript fusions as a result of chromosomal rearrangements have been a focus of attention in cancer as they provide attractive therapeutic targets. To identify novel fusion transcripts with the potential to be exploited therapeutically, researchers from the University of Texas ...
Read More »The Avian RNA-Seq Consortium: a community effort to annotate the chicken genome
Here researchers from the Roslin Institute describe how members of the chicken research community have come together as the ‘Avian RNAseq Consortium’ to provide chicken RNAseq data with a view to improving the annotation of the chicken genome. The data ...
Read More »MTide – an integrated tool for the identification of miRNA-target interaction in plants
Small RNA sequencing and degradome sequencing (also known as parallel analysis of RNA ends) have provided rich information on the microRNA (miRNA) and its cleaved mRNA targets on a genome-wide scale in plants, but no computational tools have been developed ...
Read More »RADPRE – A Computational Program for Identification of Differential mRNA Processing Including Alternative Polyadenylation
Genome-wide studies revealed the prevalence of multiple transcripts resulting from alternative polyadenylation (APA) of a single given gene in higher eukaryotes. Several studies in the past few years attempted to address how those APA events are regulated and what the ...
Read More »SNPlice – identify cis-acting, splice-modulating variants from RNA-seq datasets
The growing recognition of the importance of splicing in eukaryotes, together with rapidly accumulating RNA-sequencing data, demand robust high-throughput approaches, which efficiently analyze experimentally derived whole-transcriptome splice profiles. Researchers from The George Washington University have developed a computational approach, called ...
Read More »rMATS – Detection of differential alternative splicing from replicate RNA-Seq data
Ultra-deep RNA sequencing (RNA-Seq) has become a powerful approach for genome-wide analysis of pre-mRNA alternative splicing. Researchers from UCLA previously developed multivariate analysis of transcript splicing (MATS), a statistical method for detecting differential alternative splicing between two RNA-Seq samples. Here ...
Read More »Comparative evaluation of gene set analysis approaches for RNA-Seq data
Over the last few years transcriptome sequencing (RNA-Seq) has almost completely taken over microarrays for high-throughput studies of gene expression. Currently, the most popular use of RNA-Seq is to identify genes which are differentially expressed between two or more conditions. ...
Read More »Extensive Error in the Number of Genes Inferred from Draft Genome Assemblies
The initial publication of the genome sequence of many plants, animals, and microbes is often accompanied with great fanfare. However, these genomes are almost always first-drafts, with a lot of missing data, many gaps, and many errors in the published ...
Read More »SMITH – a LIMS for handling next-generation sequencing workflows
Wet-lab scientists of the Centre for Genomic Science and database experts from the Politecnico of Milan in the context of a Genomic Data Model Project developed SMITH a web application with a MySQL server at the backend. The data base ...
Read More »Strategies for transcriptional splice variant detection
The advent and improvement of high-throughput sequencing over the past decade leveraged the study of whole genomes and transcriptomes of different organisms at lower costs. In transcriptomics, RNA-Seq expands our capacity to understand gene expression in different tissues and pathologies, ...
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