Browsing University of Bergen Library by Journals "Bioinformatics"
Now showing items 1-6 of 6
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Extending protein interaction networks using proteoforms and small molecules
(Journal article; Peer reviewed, 2023)Motivation: Biological network analysis for high-throughput biomedical data interpretation relies heavily on topological characteristics. Networks are commonly composed of nodes representing genes or proteins that are ... -
HyperHMM: efficient inference of evolutionary and progressive dynamics on hypercubic transition graphs
(Journal article; Peer reviewed, 2023)Motivation: The evolution of bacterial drug resistance and other features in biology, the progression of cancer and other diseases and a wide range of broader questions can often be viewed as the sequential stochastic ... -
Model-based clustering of multi-tissue gene expression data
(Journal article; Peer reviewed, 2020)Motivation Recently, it has become feasible to generate large-scale, multi-tissue gene expression data, where expression profiles are obtained from multiple tissues or organs sampled from dozens to hundreds of individuals. ... -
ramr: an R/Bioconductor package for detection of rare aberrantly methylated regions
(Journal article; Peer reviewed, 2022)Motivation: With recent advances in the field of epigenetics, the focus is widening from large and frequent disease- or phenotype-related methylation signatures to rare alterations transmitted mitotically or transgenerationally ... -
Reconstructing ribosomal genes from large scale total RNA meta-transcriptomic data
(Journal article; Peer reviewed, 2020-03-13)Motivation Technological advances in meta-transcriptomics have enabled a deeper understanding of the structure and function of microbial communities. ‘Total RNA’ meta-transcriptomics, sequencing of total reverse transcribed ... -
SeeCiTe: a method to assess CNV calls from SNP arrays using trio data
(Journal article; Peer reviewed, 2021)Motivation Single nucleotide polymorphism (SNP) genotyping arrays remain an attractive platform for assaying copy number variants (CNVs) in large population-wide cohorts. However, current tools for calling CNVs are still ...