TIN: An R Package for Transcriptome Instability Analysis

TIN: An R Package for Transcriptome Instability Analysis

Blog Article

Alternative splicing is a key regulatory mechanism for gene expression, vital for the proper functioning of eukaryotic cells.Disruption of normal pre-mRNA splicing has the turbosound ts-18sw700/8a potential to cause and reinforce human disease.Owing to rapid advances in high-throughput technologies, it is now possible to identify novel mRNA isoforms and detect aberrant splicing patterns on a genome scale, across large data sets.

Analogous to the genomic types of instability describing cancer genomes (eg, chromosomal instability and microsatellite instability), transcriptome instability (TIN) has recently been proposed as a splicing-related genome-wide characteristic of certain solid cancers.We present the R package TIN, available from Bioconductor, which implements a set of methods for TIN analysis based on exon-level microarray expression profiles.TIN provides tools for estimating cga 200 to cga 510 adapter aberrant exon usage across samples and for analyzing correlation patterns between TIN and splicing factor expression levels.