Titlebook: Cancer Bioinformatics; Alexander Krasnitz Book 2019 Springer Science+Business Media, LLC, part of Springer Nature 2019 cancer informatics.

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Book 2019o attract a broad readership, ranging from active researchers in computational biology and bioinformatics developers, clinical oncologists, and anti-cancer drug developers wishing to rationalize their search for new compounds. Written in the highly successful .Methods in Molecular Biology. series fo

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Hallucinations in Parkinson’s Disease of the problem of computational genomic SV detection using next-generation sequencing (NGS) platforms, along with a brief overview of typical approaches for addressing this problem. It also discusses the general protocol that should be followed to analyze a cancer genome for SV detection in NGS data.

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https://doi.org/10.1007/978-3-658-34174-9ghts following the study of the mechanisms underlying the differential expression of these lncRNAs in association with and possibly contributing to cancer recurrence. Ultimately, the expanding knowledge of the function of lncRNAs curated by computational analysis will suggest new targets for cancer treatment.

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Neuropsychoanalytical Research,d describe the computational steps and statistical considerations going from processing of the raw array data to analysis of differential methylation. Moreover, we provide detailed guidelines on how to perform tumor subtype classification based on DNA methylation signatures.

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1064-3745 tion advice from the experts.This volume covers a wide variety of state of the art cancer-related methods and tools for data analysis and interpretation. Chapters were designed to attract a broad readership, ranging from active researchers in computational biology and bioinformatics developers, clin

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Neuropsychoanalytische Forschung,his chapter, we describe a fast and reliable analysis pipeline to study allele-specific expression in cancer using next-generation sequencing data. The pipeline provides a gene-level analysis approach that exploits paired germline DNA and tumor RNA sequencing data and benefits from parallel computation resources when available.