Preparation of the standard cell lines for reference mutations in cancer gene-panels by genome editing in HEK 293 T/17 cells

• 資料種別: 記事
• タイトル: Preparation of the standard cell lines for reference mutations in cancer gene-panels by genome editing in HEK 293 T/17 cells
• 著者・編者: Takayoshi Suzuki; Yoshinori Tsukumo; Chie Furihata
• 出版事項: 日本 : Springer Nature
• 出版年月日等: 2020-02-11
• 出版年（W3CDTF）: 2020-02-11
• タイトル（掲載誌）: Genes and environment
• 巻号年月日等（掲載誌）: 42(8)
• 掲載巻: 42(8)
• ISSN（掲載誌）: 1880-7062
• ISSN-L（掲載誌）: 1880-7046
• 本文の言語コード: eng
• DOI: 10.1186/s41021-020-0147-2; https://doi.org/10.1186/s41021-020-0147-2
• 国立国会図書館永続的識別子: info:ndljp/pid/11467648; https://dl.ndl.go.jp/pid/11467648
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 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; https://dl.ndl.go.jp/collections/B00035
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2020-03-23T18:58:42+09:00
• 保存日（W3CDTF）: 2020-03-23
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://genesenvironment.biomedcentral.com/articles
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/11467640; https://dl.ndl.go.jp/pid/11467640
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: 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; https://doi.org/10.1186/s41021-020-0147-2
• オンライン閲覧公開範囲: インターネット公開
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/11467648; https://dl.ndl.go.jp/pid/11467648; http://link.springer.com/content/pdf/10.1186/s41021-020-0147-2.pdf; http://link.springer.com/article/10.1186/s41021-020-0147-2/fulltext.html
• 参照: Next generation sequencing‐based gene panel tests for the management of solid tumors; https://cir.nii.ac.jp/crid/1360004235490456960; Use 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 Assay; https://cir.nii.ac.jp/crid/1360011145851704704; Progress in the application of CRISPR: From gene to base editing; https://cir.nii.ac.jp/crid/1360011146003108480; Validation of the Oncomine™ focus panel for next-generation sequencing of clinical tumour samples; https://cir.nii.ac.jp/crid/1360292617914353664; Complementary Versus Companion Diagnostics: Apples and Oranges?; https://cir.nii.ac.jp/crid/1360292619704944256; Feasibility and utility of a panel testing for 114 cancer‐associated genes in a clinical setting: A hospital‐based study; https://cir.nii.ac.jp/crid/1360848660420793600; A computational tool to detect DNA alterations tailored to formalin-fixed paraffin-embedded samples in cancer clinical sequencing; https://cir.nii.ac.jp/crid/1360848661771960320; Highly efficient genome editing for single-base substitutions using optimized ssODNs with Cas9-RNPs; https://cir.nii.ac.jp/crid/1360855570088300544; Targeted gene correction of α1-antitrypsin deficiency in induced pluripotent stem cells; https://cir.nii.ac.jp/crid/1360855571158050944; Next-generation sequencing-based clinical sequencing: toward precision medicine in solid tumors; https://cir.nii.ac.jp/crid/1361137044489293568; Advances in understanding cancer genomes through second-generation sequencing; https://cir.nii.ac.jp/crid/1361418519653792640; CRISPR-Cas guides the future of genetic engineering; https://cir.nii.ac.jp/crid/1361699993702540800; Precision Oncology: Who, How, What, When, and When Not?; https://cir.nii.ac.jp/crid/1361699993904008448; Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9; https://cir.nii.ac.jp/crid/1361981468972630272; Clinical Validation and Implementation of a Targeted Next-Generation Sequencing Assay to Detect Somatic Variants in Non-Small Cell Lung, Melanoma, and Gastrointestinal Malignancies; https://cir.nii.ac.jp/crid/1361981470168585728; Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis; https://cir.nii.ac.jp/crid/1361981470697723648; Analysis of error profiles in deep next-generation sequencing data; https://cir.nii.ac.jp/crid/1361981470711236352; Reference standards for next-generation sequencing; https://cir.nii.ac.jp/crid/1362544420823969792; Companion diagnostics—a tool to improve pharmacotherapy; https://cir.nii.ac.jp/crid/1362825894978571264; Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations; https://cir.nii.ac.jp/crid/1363107368704603008; A Targeted High-Throughput Next-Generation Sequencing Panel for Clinical Screening of Mutations, Gene Amplifications, and Fusions in Solid Tumors; https://cir.nii.ac.jp/crid/1363388845149368448; Guidelines for Validation of Next-Generation Sequencing–Based Oncology Panels; https://cir.nii.ac.jp/crid/1363951793258966784; Use of synthetic DNA spike-in controls (sequins) for human genome sequencing; https://cir.nii.ac.jp/crid/1364233268293297536; Companion and Complementary Diagnostics: Clinical and Regulatory Perspectives; https://cir.nii.ac.jp/crid/1364233270134448384; An Efficient Genotyping Method for Genome-modified Animals and Human Cells Generated with CRISPR/Cas9 System; https://cir.nii.ac.jp/crid/1364233270588770176
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• 書誌ID（NDLBibID）: 11467648; http://id.ndl.go.jp/bib/11467648