Preparation of the standard cell lines for reference mutations in cancer gene-panels by genome editing in HEK 293 T/17 cells
Available in National Diet Library
Find on the publisher's website
NDL Digital Collections
Digital data available
Check on the publisher's website
DOI[10.1186/s41021-020-0147-2]to the data of the same series
Holdings of Libraries in Japan
This page shows libraries in Japan other than the National Diet Library that hold the material.
Please contact your local library for information on how to use materials or whether it is possible to request materials from the holding libraries.
other
CiNii Research
Search ServiceDigitalYou can check the holdings of institutions and databases with which CiNii Research is linked at the site of CiNii Research.
Bibliographic Record
You can check the details of this material, its authority (keywords that refer to materials on the same subject, author's name, etc.), etc.
- Material Type
- 記事
- Author/Editor
- Takayoshi SuzukiYoshinori TsukumoChie Furihata
- Publication, Distribution, etc.
- Publication Date
- 2020-02-11
- Publication Date (W3CDTF)
- 2020-02-11
- Periodical title
- Genes and environment
- No. or year of volume/issue
- 42(8)
- Volume
- 42(8)
- ISSN (Periodical Title)
- 1880-7062
- ISSN-L (Periodical Title)
- 1880-7046
- Text Language Code
- eng
- DOI
- 10.1186/s41021-020-0147-2
- Persistent ID (NDL)
- info:ndljp/pid/11467648
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2020-03-23T18:58:42+09:00
- Date Captured (W3CDTF)
- 2020-03-23
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11467640
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- DOI
- 10.1186/s41021-020-0147-2
- Access Restrictions
- インターネット公開
- Related Material (URI)
- References
- Next generation sequencing‐based gene panel tests for the management of solid tumorsUse of the Ion AmpliSeq Cancer Hotspot Panel in clinical molecular pathology laboratories for analysis of solid tumours: With emphasis on validation with relevant single molecular pathology tests and the Oncomine Focus AssayProgress in the application of CRISPR: From gene to base editingValidation of the Oncomine™ focus panel for next-generation sequencing of clinical tumour samplesComplementary Versus Companion Diagnostics: Apples and Oranges?Feasibility and utility of a panel testing for 114 cancer‐associated genes in a clinical setting: A hospital‐based studyA computational tool to detect DNA alterations tailored to formalin-fixed paraffin-embedded samples in cancer clinical sequencingHighly efficient genome editing for single-base substitutions using optimized ssODNs with Cas9-RNPsTargeted gene correction of α1-antitrypsin deficiency in induced pluripotent stem cellsNext-generation sequencing-based clinical sequencing: toward precision medicine in solid tumorsAdvances in understanding cancer genomes through second-generation sequencingCRISPR-Cas guides the future of genetic engineeringPrecision Oncology: Who, How, What, When, and When Not?Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9Clinical Validation and Implementation of a Targeted Next-Generation Sequencing Assay to Detect Somatic Variants in Non-Small Cell Lung, Melanoma, and Gastrointestinal MalignanciesClinical Applications of Next-Generation Sequencing in Cancer DiagnosisAnalysis of error profiles in deep next-generation sequencing dataReference standards for next-generation sequencingCompanion diagnostics—a tool to improve pharmacotherapyGenome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulationsA Targeted High-Throughput Next-Generation Sequencing Panel for Clinical Screening of Mutations, Gene Amplifications, and Fusions in Solid TumorsGuidelines for Validation of Next-Generation Sequencing–Based Oncology PanelsUse of synthetic DNA spike-in controls (sequins) for human genome sequencingCompanion and Complementary Diagnostics: Clinical and Regulatory PerspectivesAn Efficient Genotyping Method for Genome-modified Animals and Human Cells Generated with CRISPR/Cas9 System
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossref科学研究費助成事業データベース
- Bibliographic ID (NDL)
- 11467648