UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 74

Sortiert nach

Novel genetic causes for cerebral visual impairment

European journal of human genetics : EJHG, 2015-09, Vol.24 (5), p.660-665

2015

Volltextzugriff (PDF)

Genomic epidemiology reveals transmission patterns and dynamics of SARS-CoV-2 in Aotearoa New Zealand

Nature communications, 2020-12, Vol.11 (1), p.6351-7, Article 6351

2020

Volltextzugriff (PDF)

Point mutations as a source of de novo genetic disease

Current opinion in genetics & development, 2013-06, Vol.23 (3), p.257-263

2013

Volltextzugriff (PDF)

The Genomic Scrapheap Challenge; Extracting Relevant Data from Unmapped Whole Genome Sequencing Reads, Including Strain Specific Genomic Segments, in Rats

PloS one, 2016-08, Vol.11 (8), p.e0160036-e0160036

2016

Volltextzugriff (PDF)

Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer

Science (American Association for the Advancement of Science), 2017-10, Vol.358 (6360), p.234-238

2017

Volltextzugriff (PDF)

Mapping and phasing of structural variation in patient genomes using nanopore sequencing

Nature communications, 2017-11, Vol.8 (1), p.1326-13, Article 1326

2017

Volltextzugriff (PDF)

Genetic dissection of colorectal cancer progression by orthotopic transplantation of engineered cancer organoids

Proceedings of the National Academy of Sciences - PNAS, 2017-03, Vol.114 (12), p.E2357-E2364

2017

Volltextzugriff (PDF)

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

The New England journal of medicine, 2012-11, Vol.367 (20), p.1921-1929

2012

Volltextzugriff (PDF)

Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 during Border Quarantine and Air Travel, New Zealand (Aotearoa)

Emerging infectious diseases, 2021-05, Vol.27 (5), p.1274-1278

2021

Volltextzugriff (PDF)

A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases

Cell, 2014-09, Vol.159 (1), p.200-214

2014

Volltextzugriff (PDF)

Exploring the depth and breadth of the genomics toolbox during the COVID-19 pandemic: insights from Aotearoa New Zealand

BMC medicine, 2023-06, Vol.21 (1), p.213-213, Article 213

2023

Volltextzugriff (PDF)

Real-Time Genomics for Tracking Severe Acute Respiratory Syndrome Coronavirus 2 Border Incursions after Virus Elimination, New Zealand

Emerging infectious diseases, 2021-09, Vol.27 (9), p.2361-2368

2021

Volltextzugriff (PDF)

Airborne Transmission of SARS-CoV-2 Delta Variant within Tightly Monitored Isolation Facility, New Zealand (Aotearoa)

Emerging infectious diseases, 2022-03, Vol.28 (3), p.501-509

2022

Volltextzugriff (PDF)

Genomic epidemiology of Delta SARS-CoV-2 during transition from elimination to suppression in Aotearoa New Zealand

Nature communications, 2022-07, Vol.13 (1), p.4035-4035, Article 4035

2022

Volltextzugriff (PDF)

Tracing the international arrivals of SARS-CoV-2 Omicron variants after Aotearoa New Zealand reopened its border

Nature communications, 2022-10, Vol.13 (1), p.6484-6484, Article 6484

2022

Volltextzugriff (PDF)

Genomic Evidence of In-Flight Transmission of SARS-CoV-2 Despite Predeparture Testing

Emerging infectious diseases, 2021-03, Vol.27 (3), p.687-693

2021

Volltextzugriff (PDF)

Scalable Workflows and Reproducible Data Analysis for Genomics

Methods in molecular biology (Clifton, N.J.), 2019, Vol.1910, p.723

2019

Volltextzugriff (PDF)

Use of Genomics to Track Coronavirus Disease Outbreaks, New Zealand

Emerging infectious diseases, 2021-05, Vol.27 (5), p.1317-1322

2021

Volltextzugriff (PDF)

Genomic landscape of rat strain and substrain variation

BMC genomics, 2015-05, Vol.16 (1), p.357, Article 357

2015

Volltextzugriff (PDF)

Toward effective software solutions for big biology

Nature biotechnology, 2015-07, Vol.33 (7), p.686

2015

Volltextzugriff (PDF)

Pangenome graphs in infectious disease: a comprehensive genetic variation analysis of Neisseria meningitidis leveraging Oxford Nanopore long reads

Frontiers in genetics, 2023-08, Vol.14, p.1225248-1225248

2023

Volltextzugriff (PDF)

Phylodynamics reveals the role of human travel and contact tracing in controlling the first wave of COVID-19 in four island nations

Virus evolution, 2021-11, Vol.7 (2), p.veab052

2021

Volltextzugriff (PDF)

Lack of N2-gene amplification on the Cepheid Xpert Xpress SARS-CoV-2 assay and potential novel causative mutations: A case series from Auckland, New Zealand

IDCases, 2021-01, Vol.25, p.e01233, Article e01233

2021

Volltextzugriff (PDF)

1 – 25 von 74

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(71)
Mit Volltextzugriff
(66)

Publikationsform

Artikel
(72)
Berichte
(2)

Sprache

Englisch
(74)
Japanisch
(16)

Erscheinungsjahr

n.n

Thema

Science & Technology
(62)
Life Sciences & Biomedicine
(53)
Humans
(44)
Genetics & Heredity
(29)
Female
(25)
Mutation
(24)
Male
(22)
Genomes
(18)
Animals
(15)
Genomics
(15)
Biochemistry & Molecular Biology
(14)
Covid-19
(13)
Child
(10)
Coronaviruses
(10)
Genetics
(10)
Mice
(10)
Severe Acute Respiratory Syndrome Coronavirus 2
(10)
Disease Transmission
(9)
Intellectual Disability - Genetics
(9)
Sars-Cov-2
(9)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Novel genetic causes for cerebral visual impairment

Genomic epidemiology reveals transmission patterns and dynamics of SARS-CoV-2 in Aotearoa New Zealand

Point mutations as a source of de novo genetic disease

Allelic Mutations of KITLG, Encoding KIT Ligand, Cause Asymmetric and Unilateral Hearing Loss and Waardenburg Syndrome Type 2

The Genomic Scrapheap Challenge; Extracting Relevant Data from Unmapped Whole Genome Sequencing Reads, Including Strain Specific Genomic Segments, in Rats

A Living Biobank of Breast Cancer Organoids Captures Disease Heterogeneity

Use of CRISPR-modified human stem cell organoids to study the origin of mutational signatures in cancer

Mapping and phasing of structural variation in patient genomes using nanopore sequencing

Genetic dissection of colorectal cancer progression by orthotopic transplantation of engineered cancer organoids

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 during Border Quarantine and Air Travel, New Zealand (Aotearoa)

A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases

Exploring the depth and breadth of the genomics toolbox during the COVID-19 pandemic: insights from Aotearoa New Zealand

Real-Time Genomics for Tracking Severe Acute Respiratory Syndrome Coronavirus 2 Border Incursions after Virus Elimination, New Zealand

Airborne Transmission of SARS-CoV-2 Delta Variant within Tightly Monitored Isolation Facility, New Zealand (Aotearoa)

Genomic epidemiology of Delta SARS-CoV-2 during transition from elimination to suppression in Aotearoa New Zealand

Tracing the international arrivals of SARS-CoV-2 Omicron variants after Aotearoa New Zealand reopened its border

Genomic Evidence of In-Flight Transmission of SARS-CoV-2 Despite Predeparture Testing

Scalable Workflows and Reproducible Data Analysis for Genomics

Use of Genomics to Track Coronavirus Disease Outbreaks, New Zealand

Genomic landscape of rat strain and substrain variation

Toward effective software solutions for big biology

Pangenome graphs in infectious disease: a comprehensive genetic variation analysis of Neisseria meningitidis leveraging Oxford Nanopore long reads

Phylodynamics reveals the role of human travel and contact tracing in controlling the first wave of COVID-19 in four island nations

Lack of N2-gene amplification on the Cepheid Xpert Xpress SARS-CoV-2 assay and potential novel causative mutations: A case series from Auckland, New Zealand

Suchergebnisse filtern