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Common integration sites of published datasets identified using a graph-based framework.


ABSTRACT: With next-generation sequencing, the genomic data available for the characterization of integration sites (IS) has dramatically increased. At present, in a single experiment, several thousand viral integration genome targets can be investigated to define genomic hot spots. In a previous article, we renovated a formal CIS analysis based on a rigid fixed window demarcation into a more stretchy definition grounded on graphs. Here, we present a selection of supporting data related to the graph-based framework (GBF) from our previous article, in which a collection of common integration sites (CIS) was identified on six published datasets. In this work, we will focus on two datasets, ISRTCGD and ISHIV, which have been previously discussed. Moreover, we show in more detail the workflow design that originates the datasets.

SUBMITTER: Vasciaveo A 

PROVIDER: S-EPMC4874583 | biostudies-literature | 2016

REPOSITORIES: biostudies-literature

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Common integration sites of published datasets identified using a graph-based framework.

Vasciaveo Alessandro A   Velevska Ivana I   Politano Gianfranco G   Savino Alessandro A   Schmidt Manfred M   Fronza Raffaele R  

Computational and structural biotechnology journal 20151129


With next-generation sequencing, the genomic data available for the characterization of integration sites (IS) has dramatically increased. At present, in a single experiment, several thousand viral integration genome targets can be investigated to define genomic hot spots. In a previous article, we renovated a formal CIS analysis based on a rigid fixed window demarcation into a more stretchy definition grounded on graphs. Here, we present a selection of supporting data related to the graph-based  ...[more]

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