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...

Comprehensive analysis of neoantigens derived from structural variation across whole genomes from 2528 tumors

Genome Biology, 2023-07, Vol.24 (1), p.169-169, Article 169

2023

Volltextzugriff (PDF)

Spatiotemporal Immune Landscape of Colorectal Cancer Liver Metastasis at Single-Cell Level

Cancer discovery, 2022-01, Vol.12 (1), p.134-153

2022

Volltextzugriff (PDF)

Whole-genome sequencing of 508 patients identifies key molecular features associated with poor prognosis in esophageal squamous cell carcinoma

Cell research, 2020-10, Vol.30 (10), p.902-913

2020

Volltextzugriff (PDF)

Single-cell gene fusion detection by scFusion

Nature communications, 2022-02, Vol.13 (1), p.1084-12, Article 1084

2022

Volltextzugriff (PDF)

Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants

Nucleic acids research, 2016-07, Vol.44 (13), p.6274-6286

2016

Volltextzugriff (PDF)

Single-cell transcriptomic analysis suggests two molecularly subtypes of intrahepatic cholangiocarcinoma

Nature communications, 2022-03, Vol.13 (1), p.1642-1642

2022

Volltextzugriff (PDF)

Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations

Nature communications, 2017-05, Vol.8 (1), p.15290-11, Article 15290

2017

Volltextzugriff (PDF)

Global immune characterization of HBV/HCV-related hepatocellular carcinoma identifies macrophage and T-cell subsets associated with disease progression

Cell discovery, 2020-12, Vol.6 (1), p.90-15, Article 90

2020

Volltextzugriff (PDF)

Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes

Cell, 2013-05, Vol.153 (4), p.919-929

2013

Volltextzugriff (PDF)

CCL15 Recruits Suppressive Monocytes to Facilitate Immune Escape and Disease Progression in Hepatocellular Carcinoma

Hepatology (Baltimore, Md.), 2019-01, Vol.69 (1), p.143-159

2019

Volltextzugriff (PDF)

Detecting virus integration sites based on multiple related sequencing data by VirTect

BMC medical genomics, 2019-01, Vol.12 (Suppl 1), p.19-19, Article 19

2019

Volltextzugriff (PDF)

Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes

Genome research, 2013-02, Vol.23 (2), p.217-227

2013

Volltextzugriff (PDF)

TAGET: a toolkit for analyzing full-length transcripts from long-read sequencing

Nature communications, 2023-09, Vol.14 (1), p.5935-5935, Article 5935

2023

Volltextzugriff (PDF)

Publisher Correction: Single-cell transcriptomic analysis suggests two molecularly distinct subtypes of intrahepatic cholangiocarcinoma

Nature communications, 2022-05, Vol.13 (1), p.2848-2848, Article 2848

2022

Volltextzugriff (PDF)

Systematic identification of synergistic drug pairs targeting HIV

Nature biotechnology, 2012-11, Vol.30 (11), p.1125-1130

2012

Volltextzugriff (PDF)

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.E1128-E1136

2011

Volltextzugriff (PDF)

Global impact of somatic structural variation on the DNA methylome of human cancers

Genome Biology, 2019-10, Vol.20 (1), p.209-209, Article 209

2019

Volltextzugriff (PDF)

The shaping of cancer genomes with the regional impact of mutation processes

Experimental and Molecular Medicine, 2022, 54(0), , pp.1-12

2022

Volltextzugriff (PDF)

A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases

Cell reports (Cambridge), 2018-07, Vol.24 (2), p.515-527

2018

Volltextzugriff (PDF)

Single-cell transcriptomic analysis suggests two molecularly distinct subtypes of intrahepatic cholangiocarcinoma

Nature communications, 2022-03, Vol.13 (1), Article 1642

2022

Volltextzugriff (PDF)

De novo identification of expressed cancer somatic mutations from single-cell RNA sequencing data

Genome medicine, 2023-12, Vol.15 (1), p.115-18, Article 115

2023

Volltextzugriff (PDF)

Evolutionary dependency of cancer mutations in gene pairs inferred by nonsynonymous-synonymous mutation ratios

Genome medicine, 2024-08, Vol.16 (1), p.1-20

2024

Volltextzugriff (PDF)

Multi-model analysis of gallbladder cancer reveals the role of OxLDL-absorbing neutrophils in promoting liver invasion

Experimental hematology & oncology, 2024-05, Vol.13 (1), p.58-20, Article 58

2024

Volltextzugriff (PDF)

1 – 25 von 123

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(105)
Mit Volltextzugriff
(108)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(91)
Life Sciences & Biomedicine
(54)
Humans
(37)
Technology
(26)
Genomes
(23)
Physical Sciences
(20)
Mutation
(18)
Science & Technology - Other Topics
(17)
Algorithms
(16)
Computer Science
(16)
Cancer
(15)
Chemistry
(14)
Animals
(13)
Biochemistry & Molecular Biology
(13)
Genomics
(13)
Tumors
(13)
Cell Biology
(12)
Multidisciplinary Sciences
(12)
Genetic Aspects
(11)
Biotechnology & Applied Microbiology
(10)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Nature
(9)
Nature Communications
(7)
Angewandte Chemie
(5)
Angewandte Chemie International Edition
(5)
Nature Genetics
(4)
Bioinformatics
(3)
Cell
(3)
Cell Research
(3)
Cell Research/cell Research
(3)
Genome Biology
(3)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Comprehensive analysis of neoantigens derived from structural variation across whole genomes from 2528 tumors

Spatiotemporal Immune Landscape of Colorectal Cancer Liver Metastasis at Single-Cell Level

Whole-genome sequencing of 508 patients identifies key molecular features associated with poor prognosis in esophageal squamous cell carcinoma

Single-cell gene fusion detection by scFusion

Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants

Single-cell transcriptomic analysis suggests two molecularly subtypes of intrahepatic cholangiocarcinoma

Genomic analysis of oesophageal squamous-cell carcinoma identifies alcohol drinking-related mutation signature and genomic alterations

Global immune characterization of HBV/HCV-related hepatocellular carcinoma identifies macrophage and T-cell subsets associated with disease progression

Diverse Mechanisms of Somatic Structural Variations in Human Cancer Genomes

CCL15 Recruits Suppressive Monocytes to Facilitate Immune Escape and Disease Progression in Hepatocellular Carcinoma

Detecting virus integration sites based on multiple related sequencing data by VirTect

Comprehensive analysis of the chromatin landscape in Drosophila melanogaster

Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes

TAGET: a toolkit for analyzing full-length transcripts from long-read sequencing

Publisher Correction: Single-cell transcriptomic analysis suggests two molecularly distinct subtypes of intrahepatic cholangiocarcinoma

Systematic identification of synergistic drug pairs targeting HIV

Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Global impact of somatic structural variation on the DNA methylome of human cancers

The shaping of cancer genomes with the regional impact of mutation processes

A Pan-Cancer Compendium of Genes Deregulated by Somatic Genomic Rearrangement across More Than 1,400 Cases

Single-cell transcriptomic analysis suggests two molecularly distinct subtypes of intrahepatic cholangiocarcinoma

De novo identification of expressed cancer somatic mutations from single-cell RNA sequencing data

Evolutionary dependency of cancer mutations in gene pairs inferred by nonsynonymous-synonymous mutation ratios

Author Correction: Whole-genome sequencing of 508 patients identifies key molecular features associated with poor prognosis in esophageal squamous cell carcinoma

Multi-model analysis of gallbladder cancer reveals the role of OxLDL-absorbing neutrophils in promoting liver invasion

Suchergebnisse filtern