{"id":402162,"date":"2024-10-20T04:59:52","date_gmt":"2024-10-20T04:59:52","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bs-iso-22942-12022\/"},"modified":"2024-10-26T08:52:13","modified_gmt":"2024-10-26T08:52:13","slug":"bs-iso-22942-12022","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bs-iso-22942-12022\/","title":{"rendered":"BS ISO 22942-1:2022"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
2<\/td>\n | undefined <\/td>\n<\/tr>\n | ||||||
7<\/td>\n | Foreword <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | Introduction <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | 4 Principle 5 Development of an isoPCR method 5.1 General 5.2 Intended purpose 5.3 Scientific basis <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | 5.4 Units of measurement 5.5 Method validation 5.6 Performance criteria 5.6.1 General 5.6.2 Sensitivity <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | 5.6.3 Nucleic acid extract quality 5.6.4 Applicability 5.6.5 Nucleic acid sequence specificity 5.6.6 Precision <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | 5.6.7 Accuracy 5.6.8 Selectivity 5.6.9 Linearity 5.6.10 Limit of detection (LOD) <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | 5.6.11 Limit of quantification (LOQ) <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | 5.6.12 Range 5.6.13 Robustness <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | 6 General laboratory and procedural requirements 6.1 Competence 6.2 Sample preparation 6.2.1 General 6.2.2 Obtaining a representative sample 6.2.3 Preparation of the test portion <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | 6.2.4 Nucleic acid extraction 6.3 Use of controls 6.3.1 General 6.3.2 Environmental controls 6.3.3 Positive controls 6.3.4 Negative controls 6.3.5 Extraction controls <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | 6.4 Workspace organization 6.4.1 General 6.4.2 Design of the workspace \u2014 Laboratory design 6.4.3 Design of non-laboratory workspaces 6.4.4 Personnel <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | 6.4.5 Apparatus and equipment 7 Materials and reagents 8 Interpretation of results 8.1 General 8.2 Interpretation of controls <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | 8.3 Expression of results 8.3.1 General 8.3.2 Expression of a negative result <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | 8.3.3 Expression of a positive result 8.3.4 Expression of quantitative results 8.3.5 Expression of ambiguous results 9 Test report <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | Annex A (informative) Minimum information for an isoPCR experiment (MIIPCRE) <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | Annex B (normative) Use of controls <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | Annex C (informative) Examples of isothermal nucleic acid isoPCR amplification results <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | Annex D (informative) Loop mediated isothermal amplification (LAMP) <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | Annex E (informative) Rolling circle amplification (RCA) <\/td>\n<\/tr>\n | ||||||
35<\/td>\n | Annex F (informative) Helicase dependent amplification (HDA) <\/td>\n<\/tr>\n | ||||||
37<\/td>\n | Annex G (informative) Recombinase polymerase amplification (RPA) <\/td>\n<\/tr>\n | ||||||
39<\/td>\n | Annex H (informative) Strand displacement amplification (SDA) <\/td>\n<\/tr>\n | ||||||
41<\/td>\n | Annex I (informative) Nucleic acid sequence based amplification (NASBA) <\/td>\n<\/tr>\n | ||||||
44<\/td>\n | Annex J (informative) Cas9nAR amplification <\/td>\n<\/tr>\n | ||||||
46<\/td>\n | Bibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" Molecular biomarker analysis. Isothermal polymerase chain reaction (isoPCR) methods – General requirements<\/b><\/p>\n |