Janus-a comprehensive tool investigating the two faces of transcription

被引:1
作者
Barann, Matthias [1 ]
Esser, Daniela [1 ]
Klostermeier, Ulrich C. [1 ]
Lappalainen, Tuuli [2 ]
Luzius, Anne [1 ]
Kuiper, Jan W. P. [1 ]
Ammerpohl, Ole [3 ]
Vater, Inga [3 ]
Siebert, Reiner [3 ]
Amstislavskiy, Vyacheslav [4 ]
Sudbrak, Ralf [4 ]
Lehrach, Hans [4 ,5 ]
Schreiber, Stefan [1 ]
Rosenstiel, Philip [1 ]
机构
[1] Univ Kiel, ICMB, D-24105 Kiel, Germany
[2] Univ Geneva, Sch Med, Dept Genet Med & Dev, CH-1211 Geneva 4, Switzerland
[3] Univ Kiel, Inst Human Genet, D-24105 Kiel, Germany
[4] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[5] Dahlem Ctr Genome Res & Med Syst Biol, D-14195 Berlin, Germany
关键词
CLASSICAL HODGKIN LYMPHOMA; ANTISENSE TRANSCRIPTION; MOUSE; REVEALS; GENES; MAP;
D O I
10.1093/bioinformatics/btt185
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Protocols to generate strand-specific transcriptomes with next-generation sequencing platforms have been used by the scientific community roughly since 2008. Strand-specific reads allow for detection of antisense events and a higher resolution of expression profiles enabling extension of current transcript annotations. However, applications making use of this strandedness information are still scarce. Results: Here we present a tool (Janus), which focuses on the identification of transcriptional active regions in antisense orientation to known and novel transcribed elements of the genome. Janus can compare the antisense events of multiple samples and assigns scores to identify mutual expression of either transcript in a sense/antisense pair, which could hint to regulatory mechanisms. Janus is able to make use of single-nucleotide variant (SNV) and methylation data, if available, and reports the sense to antisense ratio of regions in the vicinity of the identified genetic and epigenetic variation. Janus interrogates positions of heterozygous SNVs to identify strand-specific allelic imbalance.
引用
收藏
页码:1600 / 1606
页数:7
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