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...

An open resource for accurately benchmarking small variant and reference calls

Nature biotechnology, 2019-05, Vol.37 (5), p.561-566

2019

Volltextzugriff (PDF)

Chromosome-scale, haplotype-resolved assembly of human genomes

Nature biotechnology, 2021-03, Vol.39 (3), p.309-312

2021

Volltextzugriff (PDF)

Assembly and annotation of an Ashkenazi human reference genome

Genome Biology, 2020-06, Vol.21 (1), p.129-18, Article 129

2020

Volltextzugriff (PDF)

Genome-wide reconstruction of complex structural variants using read clouds

Nature methods, 2017-09, Vol.14 (9), p.915-920

2017

Volltextzugriff (PDF)

LongTR: genome-wide profiling of genetic variation at tandem repeats from long reads

Genome Biology, 2024-07, Vol.25 (1), p.1-12, Article 176

2024

Volltextzugriff (PDF)

Effects of temperature, acyl chain length, and flow-rate ratio on liposome formation and size in a microfluidic hydrodynamic focusing device

Soft matter, 2010-01, Vol.6 (6), p.1352

2010

Volltextzugriff (PDF)

svviz: a read viewer for validating structural variants

Bioinformatics (Oxford, England), 2015-12, Vol.31 (24), p.3994-3996

2015

Volltextzugriff (PDF)

A diploid assembly-based benchmark for variants in the major histocompatibility complex

Nature communications, 2020-09, Vol.11 (1), p.4794-4794, Article 4794

2020

Volltextzugriff (PDF)

svclassify: a method to establish benchmark structural variant calls

BMC genomics, 2016-01, Vol.17 (1), p.64-64, Article 64

2016

Volltextzugriff (PDF)

Measuring silver nanoparticle dissolution in complex biological and environmental matrices using UV–visible absorbance

Analytical and bioanalytical chemistry, 2011-10, Vol.401 (6), p.1993-2002

2011

Volltextzugriff (PDF)

Measuring Agglomerate Size Distribution and Dependence of Localized Surface Plasmon Resonance Absorbance on Gold Nanoparticle Agglomerate Size Using Analytical Ultracentrifugation

ACS nano, 2011-10, Vol.5 (10), p.8070-8079

2011

Volltextzugriff (PDF)

Medical implications of technical accuracy in genome sequencing

Genome medicine, 2016-03, Vol.8 (1), p.24-24, Article 24

2016

Volltextzugriff (PDF)

FixItFelix: improving genomic analysis by fixing reference errors

Genome Biology, 2023-02, Vol.24 (1), p.31-21, Article 31

2023

Volltextzugriff (PDF)

Best practices for evaluating single nucleotide variant calling methods for microbial genomics

Frontiers in genetics, 2015-07, Vol.6, p.235-235

2015

Volltextzugriff (PDF)

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

Nature biotechnology, 2014-03, Vol.32 (3), p.246-251

2014

Volltextzugriff (PDF)

Synthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing

PloS one, 2012-07, Vol.7 (7), p.e41356-e41356

2012

Volltextzugriff (PDF)

A crowdsourced set of curated structural variants for the human genome

PLoS computational biology, 2020-06, Vol.16 (6), p.e1007933

2020

Volltextzugriff (PDF)

Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

Nature biotechnology, 2019-10, Vol.37 (10), p.1155-1162

2019

Volltextzugriff (PDF)

Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes

Nature biotechnology, 2020-09, Vol.38 (9), p.1044-1053

2020

Volltextzugriff (PDF)

Best practices for benchmarking germline small-variant calls in human genomes

Nature biotechnology, 2019-05, Vol.37 (5), p.555-560

2019

Volltextzugriff (PDF)

Variant calling and benchmarking in an era of complete human genome sequences

Nature reviews. Genetics, 2023-07, Vol.24 (7), p.464-483

2023

Volltextzugriff (PDF)

Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study

Nature biotechnology, 2021-09, Vol.39 (9), p.1129-1140

2021

Volltextzugriff (PDF)

Challenging a bioinformatic tool's ability to detect microbial contaminants using in silico whole genome sequencing data

PeerJ (San Francisco, CA), 2017-09, Vol.5, p.e3729-e3729, Article e3729

2017

Volltextzugriff (PDF)

Advancing Benchmarks for Genome Sequencing

Cell systems, 2015-09, Vol.1 (3), p.176-177

2015

Volltextzugriff (PDF)

Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes

Nature methods, 2023-08, Vol.20 (8), p.1213-1221

2023

Volltextzugriff (PDF)

1 – 25 von 74

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(71)
Mit Volltextzugriff
(53)

Publikationsform

Sprache

Englisch
(74)
Japanisch
(16)

Erscheinungsjahr

n.n

Thema

Science & Technology
(59)
Life Sciences & Biomedicine
(41)
Humans
(31)
Genomes
(24)
Genomics
(21)
Biotechnology & Applied Microbiology
(17)
Chemistry
(17)
Dna Sequencing
(16)
Physical Sciences
(16)
Genome, Human
(15)
Genetics & Heredity
(12)
High-Throughput Nucleotide Sequencing - Methods
(12)
Algorithms
(11)
Chemistry, Analytical
(10)
Biochemistry & Molecular Biology
(9)
High-Throughput Nucleotide Sequencing
(9)
Science & Technology - Other Topics
(9)
Sequence Analysis, Dna - Methods
(9)
Software
(9)
Analytical Chemistry
(8)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

An open resource for accurately benchmarking small variant and reference calls

Chromosome-scale, haplotype-resolved assembly of human genomes

Assembly and annotation of an Ashkenazi human reference genome

Genome-wide reconstruction of complex structural variants using read clouds

LongTR: genome-wide profiling of genetic variation at tandem repeats from long reads

Effects of temperature, acyl chain length, and flow-rate ratio on liposome formation and size in a microfluidic hydrodynamic focusing device

svviz: a read viewer for validating structural variants

A diploid assembly-based benchmark for variants in the major histocompatibility complex

svclassify: a method to establish benchmark structural variant calls

Measuring silver nanoparticle dissolution in complex biological and environmental matrices using UV–visible absorbance

Measuring Agglomerate Size Distribution and Dependence of Localized Surface Plasmon Resonance Absorbance on Gold Nanoparticle Agglomerate Size Using Analytical Ultracentrifugation

Medical implications of technical accuracy in genome sequencing

FixItFelix: improving genomic analysis by fixing reference errors

Best practices for evaluating single nucleotide variant calling methods for microbial genomics

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

Synthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing

A crowdsourced set of curated structural variants for the human genome

Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes

Best practices for benchmarking germline small-variant calls in human genomes

Variant calling and benchmarking in an era of complete human genome sequences

Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study

Challenging a bioinformatic tool's ability to detect microbial contaminants using in silico whole genome sequencing data

Advancing Benchmarks for Genome Sequencing

Multiscale analysis of pangenomes enables improved representation of genomic diversity for repetitive and clinically relevant genes

Suchergebnisse filtern