Dies ist eine Übersicht möglicher Bachelor-, Master- oder Projektarbeitsthemen am Lehrstuhl für RNA Bioinformatik und Hochdurchsatzanalyse.
Ein paar Anmerkungen:
- Die Themen sind forschungsbedingt auf Englisch.
- Die Liste ist nicht vollständig.
- Die Themen sind nicht starr und können noch verändert und angepasst werden.
- Die Themen sind nicht im Detail beschrieben.
- Manche Themen können sowohl als Bachelor- als auch als Masterarbeit bearbeitet werden.
- Die Liste ist nicht immer auf dem neuesten Stand.
Wer Interesse an einem Thema hat, meldet sich bitte per Mail oder kommt direkt am Lehrstuhl vorbei, um die Details abzuklären.
Analysis of host/virus sequencing data: differential alternative splicing during viral infections. Alternative splicing plays crucial roles during many biological processes. Especially, when a host system is challenged by a viral infection, the splicing machinery seems to be disturbed. However, it is not understood on a large scale how viral infections affect the splicing machinery and result in differential expressed isoforms. We want to use transcriptomic (RNA-Seq) datasets publicly available from databases as the NCBI SRA to screen for differential alternative splicing events (such as intron retention, exon skipping, …) and to identify genes, that are generally affected during viral infections.
Sequencing data analysis and method development
Pan-genome pipeline: calculation of bacterial core gene sets (or “dudes”).Defining the core gene set, so the genes that are common among many species (or bacterial strains), is still a challenging task. Although computational tools already exist (Roary, BPGA, panX, …), an easy-to-use pipeline that starts with bacterial genomes as input and automizes all steps from the annotation, clustering, visualization of the results and the downstream analyses (such as phylogeny) is needed. In a pilot project, we already showed that combining sequence homology output and ILPs to resolve gene clusters can outperform current workflows. Here, you can help to test and extend our preliminary pipeline called RIBAP (written in python).
Differential isoform expression analysis by combining short- and long-read data. Long-read sequencing, as provided by Oxford Nanopore Technologies (ONT), is not only revolutionizing genomics but also the way we are able to analyze transcriptomes nowadays. With nanopores, we can for the first time directly sequence native RNA and therefore transcripts in their entirety. Especially for non-model organisms with no available genome sequence, sequencing the transcriptome can directly help to tackle various biological questions. We want to combine short- (Illumina) and long-read (ONT) transcriptomic data to characterize and quantify isoforms de novo.
Identification and annotation of plasmids. Plasmids are most commonly found as small circular, double-stranded DNA molecules in bacteria. In nature, they often carry genes that may benefit the survival of an organism, for example, antibiotic resistance. We want to evaluate current computational tools for plasmid annotation and aim to establish a pipeline for the automatic identification and annotation of plasmids, that should be inspired by the Mitos (http://mitos2.bioinf.uni-leipzig.de) web service for the specific annotation of mitochondrial genomes. An easy-to-use workflow and a comprehensive visualization of the annotations will be crucial parts.
Machine learning techniques to characterize microbial communities based on their metagenome. Our aim is to use machine learning techniques such as neural nets to characterize microbial communities based on their metagenome. We then use these insights to make predictions about diseases as well as other phenotypes. We employ a wide range of wet and dry lab techniques, from Nanopore sequencing and large-scale genome comparison to modern deep learning frameworks. See[bibtex file=https://raw.githubusercontent.com/rnajena/literature/master/webpage_literature.bib key=Viehweger:19]