TY - JOUR T1 - ChimPipe: Accurate detection of fusion genes and transcription-induced chimeras from RNA-seq data JF - bioRxiv DO - 10.1101/070888 SP - 070888 AU - Bernardo Rodríguez-Martín AU - Emilio Palumbo AU - Santiago Marco-Sola AU - Thasso Griebel AU - Paolo Ribeca AU - Graciela Alonso AU - Alberto Rastrojo AU - Begoña Aguado AU - Roderic Guigó AU - Sarah Djebali Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/08/22/070888.abstract N2 - Background Chimeric transcripts are commonly defined as transcripts linking two or more different genes in the genome, and can be explained by various biological mechanisms such as genomic rearrangement, read-through or trans-splicing, but also by technical or biological artefacts. Several studies have shown their importance in cancer, cell pluripotency and motility. Many programs have recently been developed to identify chimeras from Illumina RNA-seq data (mostly fusion genes in cancer). However outputs of different programs on the same dataset can be widely inconsistent, and tend to include many false positives. Other issues relate to simulated datasets restricted to fusion genes, real datasets with limited numbers of validated cases, result inconsistencies between simulated and real datasets, and gene rather than junction level assessment.Results Here we present ChimPipe, a modular and easy-to-use method to reliably identify chimeras from paired-end Illumina RNA-seq data. We have also produced realistic simulated datasets for three different read lengths, and enhanced two gold-standard cancer datasets by associating exact junction points to validated gene fusions. Benchmarking ChimPipe together with four other state-of-the-art tools on this data showed ChimPipe to be the top program at identifying exact junction coordinates for both kinds of datasets, and the one showing the best trade-off between sensitivity and precision. Applied to 106 ENCODE human RNA-seq datasets, ChimPipe identified 137 high confidence chimeras connecting the protein coding sequence of their parent genes. In subsequent experiments, three out of four predicted chimeras, two of which recurrently expressed in a large majority of the samples, could be validated. Cloning and sequencing of the three cases revealed several new chimeric transcript structures, 3 of which with the potential to encode a chimeric protein for which we hypothesized a new role.Conclusions ChimPipe combines spanning and paired end RNA-seq reads to detect any kind of chimeras, including read-throughs, and shows an excellent trade-off between sensitivity and precision. The chimeras found by ChimPipe can be validated in-vitro with high accuracy.- EST =Expressed Sequence Tag- cDNA =complementary DNA- mRNA =messenger RNA- 3D =three dimensional- RT-PCR =reverse transcriptase polymerase chain reaction- PE =paired end-bp =base pair-kb =kilobase-RAM =random access memory-Gb =Gigabyte ER -