BS ISO 20397-1:2022
$142.49
Biotechnology. Massively parallel sequencing – Nucleic acid and library preparation
Published By | Publication Date | Number of Pages |
BSI | 2022 | 24 |
PDF Catalog
PDF Pages | PDF Title |
---|---|
2 | undefined |
7 | Foreword |
8 | Introduction |
9 | 1 Scope 2 Normative references 3 Terms and definitions |
10 | 4 Nucleic acid sample quality evaluation 4.1 General |
11 | 4.2 Sample quantification 4.3 Sample purity 4.4 Sample integrity 4.4.1 General 4.4.2 Agarose gel electrophoresis 4.4.3 Capillary gel electrophoresis 4.4.4 Microfluidic analysis system 4.4.5 PCR method |
12 | 5 Nucleic acid library preparation 5.1 General 5.2 Fragmentation 5.2.1 General 5.2.2 Mechanical fragmentation 5.2.3 Enzymatic fragmentation |
13 | 5.2.4 Chemical fragmentation 5.2.5 Fragmented nucleic acid sample quantity 5.2.6 Fragmented nucleic acid sample purity 5.2.7 Fragmented nucleic acid size distribution 5.2.8 Fragmented nucleic acid purification using gel electrophoresis 5.3 Addition of universal sequences 5.3.1 Repair 5.3.2 Ligation of adapter |
14 | 5.3.3 Barcoding/indexing 5.4 Size selection 5.5 Amplification 5.6 Purification and clean up procedures |
15 | 5.7 Library quantification 5.7.1 Library quantification method 5.7.2 Selection of quantification method 5.8 Library qualification 5.8.1 General 5.8.2 Methods 6 Validation |
16 | 7 Reference materials or controls 7.1 General 7.2 Control samples 7.3 Positive control |
17 | 7.4 Negative control 7.5 No-template control 7.6 Spike-in control 7.7 Reference materials 8 Contaminations 8.1 General 8.2 Primary sample evaluation |
18 | 8.3 Protocol and operation procedure |
19 | Annex A (informative) Checklist for sample quality assessment before library construction |
20 | Annex B (informative) Examples of quality criteria for selected MPS platforms and applications |
22 | Annex C (informative) Reference material list |
23 | Bibliography |