Use of an Integrated Pan-Cancer Oncology Enrichment Next-Generation Sequencing Assay to Measure Tumour Mutational Burden and Detect Clinically Actionable Variants
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1179-2000
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Use of an Integrated Pan-Cancer Oncology Enrichment Next-Generation Sequencing Assay to Measure Tumour Mutational Burden and Detect Clinically Actionable Variants ; volume:24 ; number:3 ; day:18 ; month:4 ; year:2020 ; pages:339-349 ; date:6.2020
Molecular diagnosis & therapy ; 24, Heft 3 (18.4.2020), 339-349, 6.2020
- Creator
-
Pestinger, Valerie
Smith, Matthew
Sillo, Toju
Findlay, John M.
Laes, Jean-Francois
Martin, Gerald
Middleton, Gary
Taniere, Phillipe
Beggs, Andrew D.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s40291-020-00462-x
- URN
-
urn:nbn:de:101:1-2020090420315740930358
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:44 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Pestinger, Valerie
- Smith, Matthew
- Sillo, Toju
- Findlay, John M.
- Laes, Jean-Francois
- Martin, Gerald
- Middleton, Gary
- Taniere, Phillipe
- Beggs, Andrew D.
- SpringerLink (Online service)
Other Objects (12)
Correction to: Use of an Integrated Pan-Cancer Oncology Enrichment Next-Generation Sequencing Assay to Measure Tumour Mutational Burden and Detect Clinically Actionable Variants
Mutational landscape of pan-cancer patients with PIK3CA alterations in Chinese population
Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients
Next-generation fungal identification using target enrichment and Nanopore sequencing
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
Comprehensive assessment of actionable genomic alterations in primary colorectal carcinoma using targeted next-generation sequencing
Mutational concordance between primary and metastatic melanoma: a next-generation sequencing approach
Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing
Machine actionable metadata models
Next-Generation Sequencing Analysis of Cell-Free DNA Identifies Actionable Alterations and Genomic Features in Pediatric Cancers
Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing
Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses
Correction to: Use of an Integrated Pan-Cancer Oncology Enrichment Next-Generation Sequencing Assay to Measure Tumour Mutational Burden and Detect Clinically Actionable Variants
Mutational landscape of pan-cancer patients with PIK3CA alterations in Chinese population
Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients
Next-generation fungal identification using target enrichment and Nanopore sequencing
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
Comprehensive assessment of actionable genomic alterations in primary colorectal carcinoma using targeted next-generation sequencing
Mutational concordance between primary and metastatic melanoma: a next-generation sequencing approach
Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing
Machine actionable metadata models
Next-Generation Sequencing Analysis of Cell-Free DNA Identifies Actionable Alterations and Genomic Features in Pediatric Cancers
Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing
Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses
Correction to: Use of an Integrated Pan-Cancer Oncology Enrichment Next-Generation Sequencing Assay to Measure Tumour Mutational Burden and Detect Clinically Actionable Variants
Mutational landscape of pan-cancer patients with PIK3CA alterations in Chinese population
Enrichment of colibactin-associated mutational signatures in unexplained colorectal polyposis patients
Next-generation fungal identification using target enrichment and Nanopore sequencing
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
Comprehensive assessment of actionable genomic alterations in primary colorectal carcinoma using targeted next-generation sequencing
Mutational concordance between primary and metastatic melanoma: a next-generation sequencing approach
Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing
Machine actionable metadata models
Next-Generation Sequencing Analysis of Cell-Free DNA Identifies Actionable Alterations and Genomic Features in Pediatric Cancers
Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing