UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture

Scientific reports, 2019-08, Vol.9 (1), p.11399-7, Article 11399

2019

Volltextzugriff (PDF)

DeepFeature: feature selection in nonimage data using convolutional neural network

Briefings in bioinformatics, 2021-11, Vol.22 (6)

2021

Volltextzugriff (PDF)

DeepInsight-3D architecture for anti-cancer drug response prediction with deep-learning on multi-omics

Scientific reports, 2023-02, Vol.13 (1), p.2483-2483, Article 2483

2023

Volltextzugriff (PDF)

Association between high immune activity and worse prognosis in uveal melanoma and low-grade glioma in TCGA transcriptomic data

BMC genomics, 2022-05, Vol.23 (1), p.351-351, Article 351

2022

Volltextzugriff (PDF)

Enhanced analysis of tabular data through Multi-representation DeepInsight

Scientific reports, 2024-06, Vol.14 (1), p.12851-12851

2024

Volltextzugriff (PDF)

Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity

Nature communications, 2015-01, Vol.6 (1), p.6120-6120, Article 6120

2015

Volltextzugriff (PDF)

Performance comparison of four commercial human whole-exome capture platforms

Scientific reports, 2015-08, Vol.5 (1), p.12742-12742, Article 12742

2015

Volltextzugriff (PDF)

Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer's disease created by integrative analysis of multi-omics data

Alzheimer's research & therapy, 2020-11, Vol.12 (1), p.145-145, Article 145

2020

Volltextzugriff (PDF)

Hierarchical Maximum Likelihood Clustering Approach

IEEE transactions on biomedical engineering, 2017-01, Vol.64 (1), p.112-122

2017

Volltextzugriff (PDF)

Quantification of multicellular colonization in tumor metastasis using exome‐sequencing data

International journal of cancer, 2020-05, Vol.146 (9), p.2488-2497

2020

Volltextzugriff (PDF)

Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance

Diabetes (New York, N.Y.), 2017-10, Vol.66 (10), p.2713-2723

2017

Volltextzugriff (PDF)

An integrative machine learning approach for prediction of toxicity-related drug safety

Life science alliance, 2018-12, Vol.1 (6), p.e201800098

2018

Volltextzugriff (PDF)

The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort

PloS one, 2014-03, Vol.9 (3), p.e92549-e92549

2014

Volltextzugriff (PDF)

A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data

BMC medical genomics, 2019-10, Vol.12 (1), p.150-150, Article 150

2019

Volltextzugriff (PDF)

Stepwise iterative maximum likelihood clustering approach

BMC bioinformatics, 2016-08, Vol.17 (1), p.319-319, Article 319

2016

Volltextzugriff (PDF)

Systematic analysis of mutation distribution in three dimensional protein structures identifies cancer driver genes

Scientific reports, 2016-05, Vol.6 (1), p.26483-26483, Article 26483

2016

Volltextzugriff (PDF)

A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome

Journal of human genetics, 2018-09, Vol.63 (9), p.957-963

2018

Volltextzugriff (PDF)

Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data

Communications biology, 2019-02, Vol.2 (1), p.77-77, Article 77

2019

Volltextzugriff (PDF)

Functional Genomics of the Cilium, a Sensory Organelle

Current biology, 2005-05, Vol.15 (10), p.935-941

2005

Volltextzugriff (PDF)

A practical method to detect SNVs and indels from whole genome and exome sequencing data

Scientific reports, 2013-07, Vol.3 (1), p.2161-2161, Article 2161

2013

Volltextzugriff (PDF)

scDeepInsight: a supervised cell-type identification method for scRNA-seq data with deep learning

Briefings in bioinformatics, 2023-09, Vol.24 (5)

2023

Volltextzugriff (PDF)

Advances in AI and machine learning for predictive medicine

Journal of human genetics, 2024-10, Vol.69 (10), p.487-497

2024

Volltextzugriff (PDF)

Assessing the feasibility of GS FLX Pyrosequencing for sequencing the Atlantic salmon genome

BMC genomics, 2008-08, Vol.9 (1), p.404-404, Article 404

2008

Volltextzugriff (PDF)

Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

Scientific reports, 2018-07, Vol.8 (1), p.10367-2, Article 10367

2018

Volltextzugriff (PDF)

1 – 25 von 64

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(62)
Mit Volltextzugriff
(53)

Publikationsform

Sprache

Englisch
(63)
Japanisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(51)
Life Sciences & Biomedicine
(33)
Humans
(32)
Science
(21)
Genomes
(20)
Humanities And Social Sciences
(19)
Multidisciplinary
(19)
Multidisciplinary Sciences
(19)
Science & Technology - Other Topics
(19)
Mutation
(18)
Genetics & Heredity
(16)
Genomics
(13)
Biomedical And Life Sciences
(12)
Cancer
(12)
Female
(12)
Gene Expression
(12)
Tumors
(12)
Genomics - Methods
(10)
Male
(10)
Medicin Och Hälsovetenskap
(10)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

DeepInsight: A methodology to transform a non-image data to an image for convolution neural network architecture

DeepFeature: feature selection in nonimage data using convolutional neural network

DeepInsight-3D architecture for anti-cancer drug response prediction with deep-learning on multi-omics

Association between high immune activity and worse prognosis in uveal melanoma and low-grade glioma in TCGA transcriptomic data

Enhanced analysis of tabular data through Multi-representation DeepInsight

Whole-genome mutational landscape of liver cancers displaying biliary phenotype reveals hepatitis impact and molecular diversity

Integrated analysis of whole genome and transcriptome sequencing reveals diverse transcriptomic aberrations driven by somatic genomic changes in liver cancers

Performance comparison of four commercial human whole-exome capture platforms

Prognosis prediction model for conversion from mild cognitive impairment to Alzheimer's disease created by integrative analysis of multi-omics data

Hierarchical Maximum Likelihood Clustering Approach

Quantification of multicellular colonization in tumor metastasis using exome‐sequencing data

Structural Basis and Genotype-Phenotype Correlations of INSR Mutations Causing Severe Insulin Resistance

An integrative machine learning approach for prediction of toxicity-related drug safety

The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort

A comparison of machine learning classifiers for dementia with Lewy bodies using miRNA expression data

Stepwise iterative maximum likelihood clustering approach

Systematic analysis of mutation distribution in three dimensional protein structures identifies cancer driver genes

A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome

Risk prediction models for dementia constructed by supervised principal component analysis using miRNA expression data

Functional Genomics of the Cilium, a Sensory Organelle

A practical method to detect SNVs and indels from whole genome and exome sequencing data

scDeepInsight: a supervised cell-type identification method for scRNA-seq data with deep learning

Advances in AI and machine learning for predictive medicine

Assessing the feasibility of GS FLX Pyrosequencing for sequencing the Atlantic salmon genome

Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

Suchergebnisse filtern