The possibility of integrating viral vectors to become a persistent part of the host genome makes them a crucial element of clinical gene therapy. However, viral integration has associated risks, such as the unintentional activation of oncogenes that can result in cancer. Therefore, the analysis of integration sites of retroviral vectors is a crucial step in developing safer vectors for therapeutic use. Here we present VISMapper, a vector integration site analysis web server, to analyze next-generation sequencing data for retroviral vector integration sites. VISMapper can be found at: http://vismapper.babelomics.org . Because it uses novel mapping algorithms VISMapper is remarkably faster than previous available programs. It also provides a...
Analysis of sites of newly integrated DNA in cellular genomes is important to several fields, but me...
Integration of new DNA into cellular genomes mediates replication of retroviruses and transposons; i...
<p>The integration of foreign DNA into target genomes is useful in many experimental settings; gene ...
Abstract Background The possibility of integrating viral vectors to become a persistent part of the ...
Abstract Background Bioinformatics tools designed to identify lentiviral or retroviral vector insert...
Background: Modern gene therapy methods have limited control over where a therapeutic viral vector i...
Integration site profiling and clonality analysis of viral vector distribution in gene therapy is a ...
Abstract Background The analysis of viral vector genomic integration sites is an important component...
Retroviral and lentiviral vectors integrate their DNA into the host cell genome leading to stable tr...
Research in gene therapy involving genome integrating vectors, now often includes analysis of vector...
International audienceIntroduction: The implication of viruses in human cancers, as well as the emer...
The question of where retroviral DNA becomes integrated in chromosomes is important for understandin...
ABSTRACT Motivation: Gene therapy with retroviral vectors can induce adverse effects when those vect...
Integration of retroviral vectors in the human genome follows non random patterns that favor inserti...
Retroviral vectors have induced subtle clonal skewing inmany gene therapy patients and severe clonal...
Analysis of sites of newly integrated DNA in cellular genomes is important to several fields, but me...
Integration of new DNA into cellular genomes mediates replication of retroviruses and transposons; i...
<p>The integration of foreign DNA into target genomes is useful in many experimental settings; gene ...
Abstract Background The possibility of integrating viral vectors to become a persistent part of the ...
Abstract Background Bioinformatics tools designed to identify lentiviral or retroviral vector insert...
Background: Modern gene therapy methods have limited control over where a therapeutic viral vector i...
Integration site profiling and clonality analysis of viral vector distribution in gene therapy is a ...
Abstract Background The analysis of viral vector genomic integration sites is an important component...
Retroviral and lentiviral vectors integrate their DNA into the host cell genome leading to stable tr...
Research in gene therapy involving genome integrating vectors, now often includes analysis of vector...
International audienceIntroduction: The implication of viruses in human cancers, as well as the emer...
The question of where retroviral DNA becomes integrated in chromosomes is important for understandin...
ABSTRACT Motivation: Gene therapy with retroviral vectors can induce adverse effects when those vect...
Integration of retroviral vectors in the human genome follows non random patterns that favor inserti...
Retroviral vectors have induced subtle clonal skewing inmany gene therapy patients and severe clonal...
Analysis of sites of newly integrated DNA in cellular genomes is important to several fields, but me...
Integration of new DNA into cellular genomes mediates replication of retroviruses and transposons; i...
<p>The integration of foreign DNA into target genomes is useful in many experimental settings; gene ...