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...

The ExAC browser: displaying reference data information from over 60 000 exomes

Nucleic acids research, 2017-01, Vol.45 (D1), p.D840-D845

2017

Volltextzugriff (PDF)

Annotation of functional variation in personal genomes using RegulomeDB

Genome research, 2012-09, Vol.22 (9), p.1790-1797

2012

Volltextzugriff (PDF)

Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

Nature genetics, 2021-02, Vol.53 (2), p.195-204

2021

Volltextzugriff (PDF)

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes

Genome research, 2013-05, Vol.23 (5), p.749-761

2013

Volltextzugriff (PDF)

Polygenic architecture of rare coding variation across 394,783 exomes

Nature (London), 2023-02, Vol.614 (7948), p.492-499

2023

Volltextzugriff (PDF)

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

Nature genetics, 2017-04, Vol.49 (4), p.504-510

2017

Volltextzugriff (PDF)

Performance comparison of exome DNA sequencing technologies

Nature biotechnology, 2011-10, Vol.29 (10), p.908-914

2011

Volltextzugriff (PDF)

Patterns of genic intolerance of rare copy number variation in 59,898 human exomes

Nature genetics, 2016-10, Vol.48 (10), p.1107-1111

2016

Volltextzugriff (PDF)

Bioinformatics challenges for personalized medicine

Bioinformatics, 2011-07, Vol.27 (13), p.1741-1748

2011

Volltextzugriff (PDF)

High temperature corrosion evaluation and lifetime prediction of porous Fe22Cr stainless steel in air in temperature range 700–900 °C

Corrosion science, 2021-08, Vol.189, p.109589, Article 109589

2021

Volltextzugriff (PDF)

Integrative omics for health and disease

Nature reviews. Genetics, 2018-05, Vol.19 (5), p.299-310

2018

Volltextzugriff (PDF)

Extensive genetic variation in somatic human tissues

Proceedings of the National Academy of Sciences - PNAS, 2012-10, Vol.109 (44), p.18018-18023

2012

Volltextzugriff (PDF)

Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine

PloS one, 2013-07, Vol.8 (7), p.e68853-e68853

2013

Volltextzugriff (PDF)

Morphology changes in Fe-Cr porous alloys upon high-temperature oxidation quantified by X-ray tomographic microscopy

Materials & design, 2022-03, Vol.215, p.110492, Article 110492

2022

Volltextzugriff (PDF)

Variation in Transcription Factor Binding among Humans

Science (American Association for the Advancement of Science), 2010-04, Vol.328 (5975), p.232-235

2010

Volltextzugriff (PDF)

Ten Simple Rules to Enable Multi-site Collaborations through Data Sharing

PLoS computational biology, 2017-01, Vol.13 (1), p.e1005278-e1005278

2017

Volltextzugriff (PDF)

CGO as a barrier layer between LSCF electrodes and YSZ electrolyte fabricated by spray pyrolysis for solid oxide fuel cells

Solid state ionics, 2017-04, Vol.302, p.113-117

2017

Volltextzugriff (PDF)

The evolutionary impact of childhood cancer on the human gene pool

Nature communications, 2024-02, Vol.15 (1), p.1881-1881, Article 1881

2024

Volltextzugriff (PDF)

Chapter 7: Pharmacogenomics

PLoS computational biology, 2012-12, Vol.8 (12), p.e1002817

2012

Volltextzugriff (PDF)

Electrochemical properties of porous Sr0.86Ti0.65Fe0.35O3 oxygen electrodes in solid oxide cells: Impedance study of symmetrical electrodes

International journal of hydrogen energy, 2019-01, Vol.44 (3), p.1827-1838

2019

Volltextzugriff (PDF)

Using ALoFT to determine the impact of putative loss-of-function variants in protein-coding genes

Nature communications, 2017-08, Vol.8 (1), p.382-11, Article 382

2017

Volltextzugriff (PDF)

Low-strain sensor based on the flexible boron-doped diamond-polymer structures

Carbon (New York), 2021-03, Vol.173, p.832-841

2021

Volltextzugriff (PDF)

Systematic functional regulatory assessment of disease-associated variants

Proceedings of the National Academy of Sciences - PNAS, 2013-06, Vol.110 (23), p.9607-9612

2013

Volltextzugriff (PDF)

Coherent functional modules improve transcription factor target identification, cooperativity prediction, and disease association

PLoS genetics, 2014-02, Vol.10 (2), p.e1004122-e1004122

2014

Volltextzugriff (PDF)

1 – 25 von 1.760

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(1.610)
Mit Volltextzugriff
(1.623)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

2 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(1.397)
Physical Sciences
(1.080)
Technology
(964)
Computer Science
(787)
Computer Science, Theory & Methods
(770)
Mathematics
(670)
Mathematics, Applied
(645)
Physics
(407)
Computer Science, Software Engineering
(378)
Physics, Condensed Matter
(212)
Computer Science, Hardware & Architecture
(202)
Materials Science
(175)
Physics, Applied
(153)
Materials Science, Multidisciplinary
(148)
Life Sciences & Biomedicine
(141)
Humans
(140)
Computer Science, Information Systems
(132)
Exact Sciences And Technology
(101)
Physics, Multidisciplinary
(89)
Condensed Matter: Electronic Structure, Electrical, Magnetic, And Optical Properties
(84)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

The ExAC browser: displaying reference data information from over 60 000 exomes

Annotation of functional variation in personal genomes using RegulomeDB

Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power

The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes

Polygenic architecture of rare coding variation across 394,783 exomes

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

Performance comparison of exome DNA sequencing technologies

Patterns of genic intolerance of rare copy number variation in 59,898 human exomes

Bioinformatics challenges for personalized medicine

Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes

High temperature corrosion evaluation and lifetime prediction of porous Fe22Cr stainless steel in air in temperature range 700–900 °C

Integrative omics for health and disease

Extensive genetic variation in somatic human tissues

Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine

Morphology changes in Fe-Cr porous alloys upon high-temperature oxidation quantified by X-ray tomographic microscopy

Variation in Transcription Factor Binding among Humans

Ten Simple Rules to Enable Multi-site Collaborations through Data Sharing

CGO as a barrier layer between LSCF electrodes and YSZ electrolyte fabricated by spray pyrolysis for solid oxide fuel cells

The evolutionary impact of childhood cancer on the human gene pool

Chapter 7: Pharmacogenomics

Electrochemical properties of porous Sr0.86Ti0.65Fe0.35O3 oxygen electrodes in solid oxide cells: Impedance study of symmetrical electrodes

Using ALoFT to determine the impact of putative loss-of-function variants in protein-coding genes

Low-strain sensor based on the flexible boron-doped diamond-polymer structures

Systematic functional regulatory assessment of disease-associated variants

Coherent functional modules improve transcription factor target identification, cooperativity prediction, and disease association

Suchergebnisse filtern