UB Paderborn / Katalog / Suche / in CDI

1 – 23 von 23

Sortiert nach

"Performance Evaluation of Variant Calling Tools for Human and Microbial Genomes"

2023 International Conference on Emerging Trends in Networks and Computer Communications (ETNCC), 2023, p.235-242

2023

Link zum Volltext

Verfügbarkeit prüfen

Whole-Exome Sequencing (WES) Analysis for ABO Subgroups Identification

2023 20th International Joint Conference on Computer Science and Software Engineering (JCSSE), 2023, p.264-269

2023

Link zum Volltext
Volltext

ArrowSAM: In-Memory Genomics Data Processing Using Apache Arrow

2020 3rd International Conference on Computer Applications & Information Security (ICCAIS), 2020, p.1-6

2020

Link zum Volltext

Verfügbarkeit prüfen

Communication-Efficient Cluster Scalable Genomics Data Processing Using Apache Arrow Flight

2022 21st International Symposium on Parallel and Distributed Computing (ISPDC), 2022, p.138-146

2022

Link zum Volltext

Verfügbarkeit prüfen

An unusual family case of ADA-SCID in Russian patients

2021 IEEE Ural-Siberian Conference on Computational Technologies in Cognitive Science, Genomics and Biomedicine (CSGB), 2021, p.450-453

2021

Link zum Volltext

Verfügbarkeit prüfen

Reconstruction of high read-depth signals from low-depth whole genome sequencing data using deep learning

2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), 2017, p.1227-1232

2017

Link zum Volltext

Verfügbarkeit prüfen

FSALE: Fast Decision-Aiding Tool in the Investigation of Salmonella Enterica Genome Assemblies

2022 International Conference on Decision Aid Sciences and Applications (DASA), 2022, p.460-464

2022

Link zum Volltext

Verfügbarkeit prüfen

A new approach for detection Alzheimer's Disease with machine learning using Whole Genomic and Single Nucleotide Polymorphism-Chip data

2021 IEEE 11th Annual Computing and Communication Workshop and Conference (CCWC), 2021, p.1535-1540

2021

Link zum Volltext

Verfügbarkeit prüfen

Scalable Pathogen Pipeline Platform (SP^3): Enabling Unified Genomic Data Analysis with Elastic Cloud Computing

2019 IEEE 12th International Conference on Cloud Computing (CLOUD), 2019, p.478-480

2019

Link zum Volltext
Volltext

A portable and scalable workflow for detecting structural variants in whole-genome sequencing data

2018 IEEE 14th International Conference on e-Science (e-Science), 2018, p.303-304

2018

Link zum Volltext
Volltext

Noise cancellation for robust copy number variation detection using next generation sequencing data

2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), 2017, p.230-236

2017

Link zum Volltext

Verfügbarkeit prüfen

Machine learning based prediction of gliomas with germline mutations obtained from whole exome sequences from TCGA and 1000 Genomes Project

2019 Third International Conference on Intelligent Computing in Data Sciences (ICDS), 2019, p.1-8

2019

Link zum Volltext

Verfügbarkeit prüfen

Validation of bcbio-nextgen Pipeline Based on NextSeq500 Exome Sequencing

2019 IEEE EMBS International Conference on Biomedical & Health Informatics (BHI), 2019, p.1-6

2019

Link zum Volltext
Volltext

Evaluation of peak calling approaches for genome-wide MBD2-based Methyl-Seq profiling

2017 IEEE 7th International Conference on Computational Advances in Bio and Medical Sciences (ICCABS), 2017, p.1-6

2017

Link zum Volltext
Volltext

ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data

2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), 2016, p.141-144

2016

Link zum Volltext

Verfügbarkeit prüfen

Risk prediction using common and rare genetic variants: Application to Type 2 diabetes

2017 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), 2017, p.1757-1760

2017

Link zum Volltext

Verfügbarkeit prüfen

A systems biology analysis for the whole genome sequencing data

2014 IEEE 4th International Conference on Computational Advances in Bio and Medical Sciences (ICCABS), 2014, p.1-6

2014

Link zum Volltext
Volltext

Prediction of DNA methylation for every CpG loci in chromosome 18 in embryonic stem cells using support vector machine

2017 13th International Computer Engineering Conference (ICENCO), 2017, p.91-94

2017

Link zum Volltext
Volltext

aWGRS: Automates paired-end whole genome re-sequencing data analysis framework

2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), 2016, p.910-916

2016

Link zum Volltext

Verfügbarkeit prüfen

Whole cancer genome analysis using an I/O aware job scheduler on high performance computing resource

2014 IEEE International Conference on Bioinformatics and Biomedicine (BIBM), 2014, p.10-11

2014

Link zum Volltext

Verfügbarkeit prüfen

Poster: A Hidden Markov Model for Copy Number Variant prediction from Whole genome resequencing data

2011 IEEE 1st International Conference on Computational Advances in Bio and Medical Sciences (ICCABS), 2011, p.260-260

2011

Link zum Volltext
Volltext

The Challenge of Scaling Genome Big Data Analysis Software on TH-2 Supercomputer

2015 15th IEEE/ACM International Symposium on Cluster, Cloud and Grid Computing, 2015, p.823-828

2015

Link zum Volltext

Verfügbarkeit prüfen

Comparative copy number variation from whole genome sequencing

2011 IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS), 2011, p.123-126

2011

Link zum Volltext
Volltext

1 – 23 von 23

Suche als RSS-Feed

Aktive Filter

PublikationsformTagungsberichte

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Mit Volltextzugriff
(10)

Sprache

Englisch
(23)

Erscheinungsjahr

n.n

Thema

Genomics
(22)
Bioinformatics
(18)
Sequential Analysis
(14)
Computer Science
(10)
Science & Technology
(10)
Technology
(10)
Whole Genome Sequencing
(9)
Computer Science, Theory & Methods
(6)
Pipelines
(5)
Whole Exome Sequencing
(5)
Cancer
(4)
Dna
(4)
Sociology
(4)
Computer Science, Artificial Intelligence
(3)
Computer Science, Hardware & Architecture
(3)
Computer Science, Interdisciplinary Applications
(3)
Conferences
(3)
Copy Number Variation
(3)
Data Models
(3)
Next Generation Sequencing
(3)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

IEEE Xplore Digital Library
(22)
ACM Digital Library Complete
(1)

Menü

Weitere Dienste

Einstellungen

"Performance Evaluation of Variant Calling Tools for Human and Microbial Genomes"

Whole-Exome Sequencing (WES) Analysis for ABO Subgroups Identification

ArrowSAM: In-Memory Genomics Data Processing Using Apache Arrow

Communication-Efficient Cluster Scalable Genomics Data Processing Using Apache Arrow Flight

An unusual family case of ADA-SCID in Russian patients

Reconstruction of high read-depth signals from low-depth whole genome sequencing data using deep learning

FSALE: Fast Decision-Aiding Tool in the Investigation of Salmonella Enterica Genome Assemblies

A new approach for detection Alzheimer's Disease with machine learning using Whole Genomic and Single Nucleotide Polymorphism-Chip data

Scalable Pathogen Pipeline Platform (SP^3): Enabling Unified Genomic Data Analysis with Elastic Cloud Computing

A portable and scalable workflow for detecting structural variants in whole-genome sequencing data

Noise cancellation for robust copy number variation detection using next generation sequencing data

Machine learning based prediction of gliomas with germline mutations obtained from whole exome sequences from TCGA and 1000 Genomes Project

Validation of bcbio-nextgen Pipeline Based on NextSeq500 Exome Sequencing

Evaluation of peak calling approaches for genome-wide MBD2-based Methyl-Seq profiling

ERDS-pe: A paired hidden Markov model for copy number variant detection from whole-exome sequencing data

Risk prediction using common and rare genetic variants: Application to Type 2 diabetes

A systems biology analysis for the whole genome sequencing data

Prediction of DNA methylation for every CpG loci in chromosome 18 in embryonic stem cells using support vector machine

aWGRS: Automates paired-end whole genome re-sequencing data analysis framework

Whole cancer genome analysis using an I/O aware job scheduler on high performance computing resource

Poster: A Hidden Markov Model for Copy Number Variant prediction from Whole genome resequencing data

The Challenge of Scaling Genome Big Data Analysis Software on TH-2 Supercomputer

Comparative copy number variation from whole genome sequencing

Aktive Filter

Suchergebnisse filtern