Visualitzant Màster Universitari en Anàlisi de Dades Òmiques per matèria "Bioinformàtica"
Ara mostrant els elements 1-9 de 9
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Association between polymorphic inversions and miRNA in cancer data
(2016-09)Inversion polymorphisms is a mechanism that involves a change in the orientation of a DNA segment within a chromosome, but there is still a lack of their association with disease. However, recently ... -
Bioinformatic tools for Big Data in Omic studies with application to genomic inversion calling and multiomic data integration
(2020-09)Motivation: The diversity and huge omics data take biology and biomedicine research and application into a big data era. Most of the current statistical analyses required to analyze omic data are not ... -
Bioinformatics Pipeline for Next Generation Sequencing Analysis in Association Studies of Idiopathic Pulmonary Fibrosis
(2015-09)A complete bioinformatics pipeline for Next Generation Sequencing (NGS) analysis has been developed and applied to study the association of called variants with susceptibility in Idiopathic Pulmonary ... -
Development of a machine learning algorithm classification tool to improve strain detection in whole genome metagenomics dataset
(2020-05-15)Metagenomics is a pioneering branch of bioinformatics that utilizes genomics techniques, like the sequencing of the DNA, in order to obtain important information about microorganisms. During the recent ... -
Evolution of mtDNA variation during canid’s domestication
(2017-09-18)The close coexistence between human beings and dogs and the efficiency in their domestication have made dogs a very interesting target for basic research. By studying the history and evolution of dogs, ... -
Integration of omics and non-omics data in pancreatic cancer research
(2018-09-17)Background: With the wide-spreading in high-throughput technologies and the arrival of omics era, new bioinformatics tools are available for the integration of different data types. Epidemiological and ... -
Novel transcript discovery in yeast using sequencing reads from Oxford Nanopore Technologies in comparison to Next Generation Sequencing
(2018-09)The advent of Oxford Nanopore Technologies is expected to play a pivotal role in near future sequencing studies. Omics data analysis and related processes, currently bound to Next Generation Sequencing, ... -
Rna sequencing role in the genetic diagnosis of hereditary breast and ovarian cancer
(2024-09-10)Hereditary breast and ovarian cancer (HBOC) is a syndrome defined by an increased risk of developing breast cancer (BC) and/or ovarian cancer (OC), mainly due to germline pathogenic variants in BRCA1 ... -
SVModeler: Simulation of human haplotypes containing synthetic structural variants
(2024-09-19)Abstract Motivation: Long-read sequencing overcomes the limits of short-reads by providing longer sequences that can span repetitive regions, improving the detection of structural variants and accurately ...