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@ARTICLE{Afzal:154647,
author = {S. Afzal$^*$ and R. Fronza and M. Schmidt$^*$},
title = {{VS}eq-{T}oolkit: {C}omprehensive {C}omputational
{A}nalysis of {V}iral {V}ectors in {G}ene {T}herapy.},
journal = {Molecular therapy Methods $\&$ clinical development [...]},
volume = {17},
issn = {2329-0501},
address = {New York, NY},
publisher = {Nature Publishing Group},
reportid = {DKFZ-2020-00910},
pages = {752 - 757},
year = {2020},
note = {2020 Mar 30;17:752-757#EA:G100#LA:G100#translationale
Onkologie},
abstract = {Viral vector characterization and analysis are important
components for the development of safe gene therapeutic
products, elucidating the potential genotoxic and
immunogenic effects of vectors and establishing their safety
profiles. Here, we present VSeq-Toolkit, which offers
varying analysis modes for viral gene therapy data. The
first mode determines the undesirable known contaminants and
their frequency in viral preparations or other sequencing
data. The second mode is designed for the analysis of
intra-vector fusion breakpoints and the third mode for
unraveling the viral-host fusion events distribution.
Analysis modes of our toolkit can be executed independently
or together and allow the analysis of multiple viral vectors
concurrently. It has been designed and evaluated for the
analysis of short read high-throughput sequencing data,
including whole-genome or targeted sequencing. VSeq-Toolkit
is developed in Perl and Bash programming languages and is
available at https://github.com/CompMeth/VSeq-Toolkit.},
cin = {G100 / B340},
ddc = {610},
cid = {I:(DE-He78)G100-20160331 / I:(DE-He78)B340-20160331},
pnm = {312 - Functional and structural genomics (POF3-312)},
pid = {G:(DE-HGF)POF3-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32346552},
pmc = {pmc:PMC7177155},
doi = {10.1016/j.omtm.2020.03.024},
url = {https://inrepo02.dkfz.de/record/154647},
}