UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 73

Sortiert nach

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

Genome Biology, 2021-10, Vol.22 (1), p.299-299, Article 299

2021

Volltextzugriff (PDF)

WhatsHap: Weighted Haplotype Assembly for Future-Generation Sequencing Reads

Journal of computational biology, 2015-06, Vol.22 (6), p.498

2015

Volltextzugriff (PDF)

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Genome Biology, 2022-01, Vol.23 (1), p.29-29, Article 29

2022

Volltextzugriff (PDF)

Hybrid-hybrid correction of errors in long reads with HERO

Genome Biology, 2023-12, Vol.24 (1), p.1-39, Article 275

2023

Volltextzugriff (PDF)

Accurate and scalable variant calling from single cell DNA sequencing data with ProSolo

Nature communications, 2021-11, Vol.12 (1), p.6744-11, Article 6744

2021

Volltextzugriff (PDF)

Overlap graph-based generation of haplotigs for diploids and polyploids

Bioinformatics, 2019-11, Vol.35 (21), p.4281-4289

2019

Volltextzugriff (PDF)

Enhancing Long-Read-Based Strain-Aware Metagenome Assembly

Frontiers in genetics, 2022-05, Vol.13, p.868280-868280

2022

Volltextzugriff (PDF)

Using the structure of genome data in the design of deep neural networks for predicting amyotrophic lateral sclerosis from genotype

Bioinformatics, 2019-07, Vol.35 (14), p.i538-i547

2019

Volltextzugriff (PDF)

Full-length de novo viral quasispecies assembly through variation graph construction

Bioinformatics (Oxford, England), 2019-12, Vol.35 (24), p.5086-5094

2019

Volltextzugriff (PDF)

Varlociraptor: enhancing sensitivity and controlling false discovery rate in somatic indel discovery

Genome Biology, 2020-04, Vol.21 (1), p.98-25, Article 98

2020

Volltextzugriff (PDF)

Ranbow: A fast and accurate method for polyploid haplotype reconstruction

PLoS computational biology, 2020-05, Vol.16 (5), p.e1007843-e1007843

2020

Volltextzugriff (PDF)

OGRE: Overlap Graph-based metagenomic Read clustEring

Bioinformatics, 2021-05, Vol.37 (7), p.905-912

2021

Volltextzugriff (PDF)

Recursive ensemble feature selection provides a robust mRNA expression signature for myalgic encephalomyelitis/chronic fatigue syndrome

Scientific reports, 2021-02, Vol.11 (1), p.4541-4541, Article 4541

2021

Volltextzugriff (PDF)

Viral quasispecies assembly via maximal clique enumeration

PLoS computational biology, 2014-03, Vol.10 (3), p.e1003515

2014

Volltextzugriff (PDF)

MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels

Bioinformatics, 2013-12, Vol.29 (24), p.3143-3150

2013

Volltextzugriff (PDF)

Using population-specific add-on polymorphisms to improve genotype imputation in underrepresented populations

PLoS computational biology, 2022-01, Vol.18 (1), p.e1009628-e1009628

2022

Volltextzugriff (PDF)

Structural variant detection in cancer genomes: computational challenges and perspectives for precision oncology

NPJ precision oncology, 2021-03, Vol.5 (1), p.15-15, Article 15

2021

Volltextzugriff (PDF)

Using hidden Markov models to analyze gene expression time course data

Bioinformatics, 2003, Vol.19 (suppl-1), p.i255-i263

2003

Volltextzugriff (PDF)

Machine Learning-Based Ensemble Recursive Feature Selection of Circulating miRNAs for Cancer Tumor Classification

Cancers, 2020-07, Vol.12 (7), p.1785

2020

Volltextzugriff (PDF)

CLEVER: clique-enumerating variant finder

Bioinformatics, 2012-11, Vol.28 (22), p.2875-2882

2012

Volltextzugriff (PDF)

MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants

iScience, 2019-08, Vol.18, p.20-27

2019

Volltextzugriff (PDF)

Discovering motifs that induce sequencing errors

BMC bioinformatics, 2013-04, Vol.14 Suppl 5 (Suppl 5), p.S1-S1, Article S1

2013

Volltextzugriff (PDF)

Repeat- and error-aware comparison of deletions

Bioinformatics, 2015-09, Vol.31 (18), p.2947-2954

2015

Volltextzugriff (PDF)

Generic Identication of Binary-Valued Hidden Markov Processes

Journal of algebraic statistics, 2014-04, Vol.5 (1)

Schönhuth, Alexander

2014

Volltextzugriff (PDF)

Efficient Tests for Equivalence of Hidden Markov Processes and Quantum Random Walks

IEEE transactions on information theory, 2011-03, Vol.57 (3), p.1746-1753

2011

Volltextzugriff (PDF)

1 – 25 von 73

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(69)
Mit Volltextzugriff
(67)

Publikationsform

Sprache

Englisch
(73)
Japanisch
(8)

Erscheinungsjahr

n.n

Thema

Science & Technology
(61)
Life Sciences & Biomedicine
(49)
Computer Science
(39)
Biochemistry & Molecular Biology
(38)
Biochemical Research Methods
(34)
Mathematical & Computational Biology
(33)
Technology
(31)
Biotechnology & Applied Microbiology
(28)
Humans
(28)
Bioinformatics
(23)
Mathematics
(23)
Physical Sciences
(23)
Statistics & Probability
(23)
Software
(22)
Computer Science, Interdisciplinary Applications
(21)
Genomes
(19)
Algorithms
(17)
Genomics
(14)
Haplotypes
(13)
Genetics
(12)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

phasebook: haplotype-aware de novo assembly of diploid genomes from long reads

WhatsHap: Weighted Haplotype Assembly for Future-Generation Sequencing Reads

Strainline: full-length de novo viral haplotype reconstruction from noisy long reads

Hybrid-hybrid correction of errors in long reads with HERO

Accurate and scalable variant calling from single cell DNA sequencing data with ProSolo

Overlap graph-based generation of haplotigs for diploids and polyploids

Enhancing Long-Read-Based Strain-Aware Metagenome Assembly

Using the structure of genome data in the design of deep neural networks for predicting amyotrophic lateral sclerosis from genotype

Full-length de novo viral quasispecies assembly through variation graph construction

Varlociraptor: enhancing sensitivity and controlling false discovery rate in somatic indel discovery

Ranbow: A fast and accurate method for polyploid haplotype reconstruction

OGRE: Overlap Graph-based metagenomic Read clustEring

Recursive ensemble feature selection provides a robust mRNA expression signature for myalgic encephalomyelitis/chronic fatigue syndrome

Viral quasispecies assembly via maximal clique enumeration

MATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indels

Using population-specific add-on polymorphisms to improve genotype imputation in underrepresented populations

Structural variant detection in cancer genomes: computational challenges and perspectives for precision oncology

Using hidden Markov models to analyze gene expression time course data

Machine Learning-Based Ensemble Recursive Feature Selection of Circulating miRNAs for Cancer Tumor Classification

CLEVER: clique-enumerating variant finder

MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants

Discovering motifs that induce sequencing errors

Repeat- and error-aware comparison of deletions

Generic Identication of Binary-Valued Hidden Markov Processes

Efficient Tests for Equivalence of Hidden Markov Processes and Quantum Random Walks

Suchergebnisse filtern