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10.1186/s12866-015-0470-0 http://scihub22266oqcxt.onion/10.1186/s12866-015-0470-0 C4487798!4487798!26129912     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMC+Microbiol 2015 ; 15 (ä): ä Nephropedia Template TP {{tp|p=26129912|t=2015. Characterization of pseudorabies virus transcriptome by Illumina sequencing |pdf=|usr=}}{{26129912}} gab.com Text Characterization of pseudorabies virus transcriptome by Illumina sequencing JO: BMC Microbiol http://www.kidney.de/pget.php?&tw=1&pmid=26129912 #FOAvip Background: Pseudorabies virus is a widely-studied model organism of the Herpesviridae family, with a compact genome arrangement of 72 known coding sequences. In order to obtain an up-to-date genetic map of the virus, a combination of RNA-sequencing approaches were applied, as recent advancements in high-throughput sequencing methods have provided a wealth of information on novel RNA species and transcript isoforms, revealing additional layers of transcriptome complexity in several viral species. Results: The total RNA content and polyadenylation landscape of pseudorabies virus were characterized for the first time at high coverage by Illumina high-throughput sequencing of cDNA samples collected during the lytic infectious cycle. As anticipated, nearly all of the viral genome was transcribed, with the exception of loci in the large internal and terminal repeats, and several small intergenic repetitive sequences. Our findings included a small novel polyadenylated non-coding RNA near an origin of replication, and the single-base resolution mapping of 3? UTRs across the viral genome. Alternative polyadenylation sites were found in a number of genes and a novel alternative splice site was characterized in the ep0 gene, while previously known splicing events were confirmed, yielding no alternative splice isoforms. Additionally, we detected the active polyadenylation of transcripts earlier believed to be transcribed as part of polycistronic RNAs. Conclusion: To the best of our knowledge, the present work has furnished the highest-resolution transcriptome map of an alphaherpesvirus to date, and reveals further complexities of viral gene expression, with the identification of novel transcript boundaries, alternative splicing of the key transactivator EP0, and a highly abundant, novel non-coding RNA near the lytic replication origin. These advances provide a detailed genetic map of PRV for future research. Electronic supplementary material: The online version of this article (doi:10.1186/s12866-015-0470-0) contains supplementary material, which is available to authorized users. Twit Text FOAVip Characterization of pseudorabies virus transcriptome by Illumina sequencing ????BMC Microbiol http://www.kidney.de/pget.php?&tw=1&pmid=26129912 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26129912 #FOAvip English Wikipedia <ref>{{Cite pmid|26129912}}</ref> Characterization of pseudorabies virus transcriptome by Illumina sequencing #MMPMID26129912 Oláh P; Tombácz D; Póka N; Csabai Z; Prazsák I; Boldogk?i Z BMC Microbiol 2015[]; 15 (ä): ä PMID26129912show ga Background: Pseudorabies virus is a widely-studied model organism of the Herpesviridae family, with a compact genome arrangement of 72 known coding sequences. In order to obtain an up-to-date genetic map of the virus, a combination of RNA-sequencing approaches were applied, as recent advancements in high-throughput sequencing methods have provided a wealth of information on novel RNA species and transcript isoforms, revealing additional layers of transcriptome complexity in several viral species. Results: The total RNA content and polyadenylation landscape of pseudorabies virus were characterized for the first time at high coverage by Illumina high-throughput sequencing of cDNA samples collected during the lytic infectious cycle. As anticipated, nearly all of the viral genome was transcribed, with the exception of loci in the large internal and terminal repeats, and several small intergenic repetitive sequences. Our findings included a small novel polyadenylated non-coding RNA near an origin of replication, and the single-base resolution mapping of 3? UTRs across the viral genome. Alternative polyadenylation sites were found in a number of genes and a novel alternative splice site was characterized in the ep0 gene, while previously known splicing events were confirmed, yielding no alternative splice isoforms. Additionally, we detected the active polyadenylation of transcripts earlier believed to be transcribed as part of polycistronic RNAs. Conclusion: To the best of our knowledge, the present work has furnished the highest-resolution transcriptome map of an alphaherpesvirus to date, and reveals further complexities of viral gene expression, with the identification of novel transcript boundaries, alternative splicing of the key transactivator EP0, and a highly abundant, novel non-coding RNA near the lytic replication origin. These advances provide a detailed genetic map of PRV for future research. Electronic supplementary material: The online version of this article (doi:10.1186/s12866-015-0470-0) contains supplementary material, which is available to authorized users. äCharacterization of pseudorabies virus transcriptome by Illumina seque(epmc).pdf DeepDyve Pubget Overpricing