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xiii | |
| About the editor |
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xvii | |
| Preface |
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xix | |
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1 Overview of healthcare biotechnology |
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1 | (26) |
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1 | (1) |
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1 | (6) |
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1.2.1 Genetic screening and testing |
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3 | (1) |
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1.2.2 Diagnosis of genetic disorders |
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3 | (3) |
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1.2.3 Pharmacogenomics and epigenomics |
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6 | (1) |
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1.2.4 Personalized medicine |
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6 | (1) |
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7 | (3) |
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1.3.1 Tools of transcriptomics |
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7 | (2) |
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1.3.2 Transcriptomics in disease diagnosis |
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9 | (1) |
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1.3.3 Transcriptome profiling in drug discovery |
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10 | (1) |
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10 | (4) |
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1.4.1 Tools and techniques in the proteomics-based study |
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10 | (3) |
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1.4.2 Biomarker discovery |
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13 | (1) |
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13 | (1) |
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14 | (6) |
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1.5.1 Tools and techniques in metabolomics study |
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16 | (2) |
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1.5.2 Metabolomics in treatment of cancer, neurological, and psychiatric disorders |
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18 | (2) |
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1.5.3 Individualized metabolomics |
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20 | (1) |
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20 | (1) |
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20 | (1) |
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20 | (7) |
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2 Three-dimensional printing in healthcare |
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27 | (14) |
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27 | (1) |
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2.2 Three-dimensional printing technology (hardware and software) |
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27 | (3) |
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2.3 Materials of three-dimensional printing |
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30 | (1) |
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2.4 Three-dimensional printing in surgical planning and medical education |
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31 | (1) |
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2.5 Three-dimensional printing in oral and maxillofacial surgery |
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32 | (1) |
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2.6 Three-dimensional printing in orthopedics |
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33 | (1) |
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2.7 Three-dimensional printing in neurosurgery |
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33 | (2) |
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2.8 Bioprinting tissue and organ fabrication |
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35 | (1) |
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2.9 Three-dimensional printing in pharmaceutical industry |
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36 | (1) |
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2.10 Future of three-dimensional printing |
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36 | (1) |
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2.10.1 Limitations of three-dimensional printings |
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37 | (1) |
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37 | (1) |
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37 | (4) |
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3 Synthetic biology in healthcare: technologies and applications |
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41 | (14) |
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41 | (1) |
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3.1.1 Cell-free systems and applications |
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41 | (1) |
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3.2 Technologies for synthetic DNA, proteins, and organisms |
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41 | (1) |
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3.2.1 Synthetic biology-based Doggybone DNA technology and its uses in vaccines and DNA-based gene therapy products |
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41 | (1) |
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3.2.2 Development of linear dbDNA vaccine construct |
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42 | (1) |
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3.3 Gen9 technology---microfluidic devices and methods for gene synthesis |
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42 | (4) |
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3.3.1 DNA synthesis and scale up (BioFab platform) |
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42 | (1) |
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3.3.2 Technologies for synthetic genomes |
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43 | (1) |
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3.3.3 Synthetic biology to create an artificial membrane-binding protein |
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43 | (1) |
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3.3.4 Pathway rewiring with adapters and scaffolds |
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44 | (1) |
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3.3.5 Synthetic DNA for developing new antibiotics |
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44 | (1) |
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3.3.6 Synthetic DNA for amino-acid replacement |
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44 | (1) |
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3.3.7 Synthetic proteins technologies |
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45 | (1) |
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3.3.8 Technologies to create synthetic organisms |
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45 | (1) |
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3.3.9 Synthetic biology applications in diagnostics |
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46 | (1) |
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3.4 Transcriptional, posttranslational, and hybrid biosensing and applications |
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46 | (1) |
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3.4.1 Transcriptional biosensing |
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46 | (1) |
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3.4.2 Posttranslational biosensing |
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46 | (1) |
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46 | (1) |
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46 | (3) |
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3.5.1 Paper-based diagnostic |
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47 | (1) |
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3.5.2 Synthetic biology applications for drug discovery and therapy |
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47 | (1) |
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3.5.3 Drug-target identification (synthetic pathways and systems) |
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48 | (1) |
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48 | (1) |
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3.5.5 Therapeutic treatment (synthetic biology devices) |
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48 | (1) |
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3.5.6 Therapeutic delivery |
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48 | (1) |
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3.6 Synthetic biology for creating living systems to produce small molecules, for instance, aspirin, that characteristically come from chemical rather than the biological processes |
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49 | (1) |
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3.6.1 CodeEvolver-like protein-engineering synthetic-biology platform to create unique enzymes as therapeutics |
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49 | (1) |
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3.6.2 Chimeric antigen receptor |
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49 | (1) |
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3.6.3 Synthetic genomes and vaccine design (SARS-CoV-2 and other viruses) |
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49 | (1) |
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3.7 Living therapies---engineering microbes and bacteriophage to treat disease |
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50 | (1) |
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3.7.1 Engineered bacteria (such as Salmonella) to deliver vaccines |
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50 | (1) |
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3.7.2 Understanding disease mechanism |
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50 | (1) |
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3.7.3 Synthetic biology-based pathway engineering for pharmaceutical production |
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50 | (1) |
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3.7.4 Constructing biosynthetic pathways |
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50 | (1) |
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3.7.5 Optimizing pathway flux |
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51 | (1) |
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3.7.6 Programming novel functionality and materials |
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51 | (1) |
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3.7.7 Chemical retrosynthesis and its future applications in healthcare |
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51 | (1) |
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3.8 Future challenges and conclusions |
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51 | (1) |
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52 | (1) |
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52 | (3) |
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4 Nanotechnology in healthcare: nanoparticles for diagnostic and therapy |
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55 | (16) |
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55 | (1) |
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4.2 Classification and properties of nanoparticles |
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56 | (3) |
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56 | (1) |
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4.2.2 Magnetic nanoparticles |
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57 | (1) |
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57 | (1) |
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4.2.4 Carbon nanostructures |
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58 | (1) |
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4.2.5 Polymeric nanoparticles |
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58 | (1) |
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4.3 Nanoparticle-based biosensors for medical diagnosis |
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59 | (2) |
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4.3.1 Plasmonic biosensors |
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59 | (1) |
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4.3.2 QD-based biosensors |
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60 | (1) |
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4.3.3 Carbon nanostructure-based biosensors |
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61 | (1) |
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4.4 Nanoparticle-based therapy and imaging |
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61 | (4) |
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4.4.1 Targeted drug delivery |
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62 | (1) |
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4.4.2 Bioimaging and photothermal therapy |
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63 | (1) |
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4.4.3 Nanoparticles in the clinic |
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64 | (1) |
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4.5 Conclusion and future perspective |
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65 | (1) |
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65 | (6) |
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5 Analysis and applications of sequencing in healthcare |
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71 | (12) |
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Maloyjo Joyraj Bhattacharjee |
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71 | (1) |
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5.2 Method of de-novo and reference-based DNA sequencing |
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71 | (1) |
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5.3 Generation of DNA reads |
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72 | (1) |
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5.4 Quality assessment of reads |
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73 | (1) |
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5.5 Trimming of DNA reads |
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74 | (1) |
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74 | (1) |
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75 | (1) |
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5.8 Analysis of DNA sequences for marker-based surveillance of diseases |
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75 | (1) |
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5.9 Phylomedicine of genetic diseases |
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76 | (1) |
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5.10 Method of de-novo and reference-based RNA sequencing |
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76 | (1) |
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5.11 Generation of short RNA reads and quality assessment |
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77 | (1) |
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5.12 Trimming of RNA reads |
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77 | (1) |
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5.13 Mapping of RNA reads |
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77 | (1) |
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5.14 Assembly of RNA reads |
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77 | (1) |
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5.15 Analysis of differential expression of genes in diseases states and in prognosis of disease |
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78 | (1) |
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5.16 Analysis of alternative splicing of genes and gene fusion in disease states |
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78 | (1) |
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5.17 Analysis of long noncoding RNA and its relevance to disease |
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78 | (1) |
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5.18 Gene coexpression analysis and annotation of TF-TFBS and gene regulatory network |
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79 | (1) |
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5.19 Method of DAP-sequencing and genome-wide annotation of cistrome |
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79 | (2) |
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5.20 Analysis of DAP sequences and its application in healthcare |
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81 | (1) |
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5.21 Genome-wide mapping of TF-TFBS and visualization of gene-regulatory network |
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81 | (1) |
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81 | (2) |
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6 Innovative technologies in precision healthcare |
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83 | (20) |
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6.1 Defining precision and personalized medicine |
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83 | (2) |
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6.1.1 Assessing emerging technologies for personalized precision medicines' clinical trials |
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83 | (1) |
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6.1.2 Biosensors in personalized medicine |
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84 | (1) |
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6.1.3 Omics in precision healthcare |
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84 | (1) |
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6.1.4 Engineering precision medicine technology and platforms |
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84 | (1) |
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6.2 Databases applications in precision healthcare |
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85 | (2) |
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6.2.1 Microbiome databases |
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85 | (1) |
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6.2.2 Databases for protein-coding genes |
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86 | (1) |
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6.2.3 Databases for noncoding genes |
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86 | (1) |
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6.2.4 Databases used for annotation of human genetic variants and rearrangements |
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86 | (1) |
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6.2.5 Prediction of gene function |
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87 | (1) |
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6.3 Bioengineering, machine learning for personalized medicine |
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87 | (3) |
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6.3.1 Principle of machine learning |
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87 | (1) |
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6.3.2 Why machine learning? |
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88 | (1) |
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6.3.3 Supervised machine learning |
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89 | (1) |
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6.3.4 Unsupervised machine learning |
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89 | (1) |
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6.3.5 Reinforcement learning |
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89 | (1) |
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90 | (1) |
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6.3.7 Recommendations in machine learning |
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90 | (1) |
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6.3.8 Testing and verification |
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90 | (1) |
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6.4 Application of bioinformatics machine learning and in-depth data analysis |
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90 | (10) |
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91 | (1) |
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6.4.2 Explore and prepare data |
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91 | (1) |
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6.4.3 Feature selection with decision trees |
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92 | (2) |
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6.4.4 Feature selection by analysis |
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94 | (1) |
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6.4.5 Analysis with edgeR or DESeq2 |
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94 | (2) |
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6.4.6 Pickup machine learning models |
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96 | (1) |
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6.4.7 Evaluate machine learning model |
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96 | (2) |
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6.4.8 Workflow for processing readings in RNA-seq |
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98 | (2) |
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100 | (1) |
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101 | (1) |
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101 | (2) |
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7 Omics applications in reproductive medicine |
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103 | (22) |
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7.1 Genetic testing and molecular methods of female infertility |
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103 | (6) |
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7.1.1 Molecular methods of transcriptome analysis in female infertility |
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103 | (1) |
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7.1.2 Methods of metabolomics analysis of female infertility |
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104 | (2) |
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7.1.3 Methods of proteomics analysis of female infertility |
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106 | (1) |
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7.1.4 Molecular methods of microbial analysis of female infertility |
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107 | (1) |
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7.1.5 Molecular methods of genomic analysis of female infertility |
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108 | (1) |
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7.2 Genetic testing and molecular methods of male infertility |
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109 | (6) |
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7.2.1 Molecular methods of transcriptome analysis of male infertility |
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110 | (1) |
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7.2.2 Methods of metabolomics analysis of male infertility |
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111 | (1) |
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7.2.3 Molecular methods of proteomic analysis of male infertility |
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111 | (1) |
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7.2.4 Molecular methods of microbial anafysis of male infertility |
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112 | (1) |
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7.2.5 Molecular methods of genomic analysis of male infertility |
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113 | (2) |
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7.3 Genetic testing and molecular methods of embryonic analysis and monitoring during the in vitro fertilization process |
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115 | (3) |
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7.3.1 Invasive preimplantation genetic testing of the embryo in the in vitro fertilization process |
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115 | (1) |
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7.3.2 Noninvasive genetic testing of embryo quality for the in vitro fertilization process from the spent blastocyst medium |
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115 | (1) |
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7.3.3 Transcriptomic analyses in spent culture medium |
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116 | (2) |
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7.4 Omics methods of infertility |
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118 | (1) |
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119 | (1) |
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119 | (6) |
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8 Biotechnology approaches in developing novel drug-delivery systems |
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125 | (22) |
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125 | (1) |
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8.1.1 Novel drug-delivery system |
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125 | (1) |
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8.2 Drug-delivery mechanism |
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126 | (1) |
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8.2.1 Passive and active targeting |
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126 | (1) |
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8.3 Basic components of a drug-delivery system |
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127 | (1) |
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8.4 Different routes of a drug-delivery system |
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128 | (3) |
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128 | (1) |
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8.4.2 Nasal and intranasal drug delivery |
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128 | (1) |
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8.4.3 Transdermal drug delivery |
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129 | (1) |
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8.4.4 Pulmonary drug delivery |
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130 | (1) |
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8.4.5 Colon-specific drug delivery |
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130 | (1) |
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8.4.6 Ophthalmic drug delivery |
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130 | (1) |
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8.4.7 Mucoadhesive drug delivery |
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130 | (1) |
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8.4.8 Osmotically controlled drug delivery |
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131 | (1) |
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131 | (12) |
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132 | (1) |
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133 | (1) |
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134 | (4) |
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138 | (1) |
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8.5.5 Protein or peptide drug-delivery system |
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139 | (1) |
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140 | (1) |
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140 | (1) |
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141 | (1) |
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141 | (1) |
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8.5.10 Microparticle-based lipids |
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142 | (1) |
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8.5.11 Herbal phytoconstituent-based novel drugs and their delivery systems |
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142 | (1) |
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143 | (1) |
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143 | (4) |
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9 Gene therapy and gene editing in healthcare |
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147 | (30) |
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9.1 Introduction: gene therapy and gene editing |
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147 | (3) |
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147 | (1) |
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9.1.2 Gene transfer strategy: delivery vehicle |
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148 | (2) |
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9.2 Gene-editing technologies |
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150 | (2) |
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150 | (1) |
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9.2.2 Zinc-finger nucleases |
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150 | (1) |
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9.2.3 Transcription activator-like effector nucleases |
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150 | (1) |
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151 | (1) |
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9.3 Clinical trials of gene therapy and gene editing (in vivo and ex vivo): an update |
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152 | (1) |
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9.4 Gene therapy and gene editing in diseases/disorders: current progress |
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152 | (15) |
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9.4.1 Gene therapy and gene editing in hemophilia |
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153 | (1) |
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9.4.2 Gene therapy and gene editing in cardiovascular disorders |
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153 | (1) |
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9.4.3 Gene therapy and gene editing in metabolic syndrome |
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154 | (1) |
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9.4.4 Gene therapy and gene editing in neurological disorders |
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154 | (1) |
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9.4.5 Gene therapy and gene editing in HIV infection |
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155 | (5) |
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9.4.6 Gene therapy and gene editing in various cancers |
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160 | (7) |
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9.5 Miscellaneous diseases and disorders |
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167 | (1) |
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9.5.1 Gene therapies in ophthalmic disease |
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168 | (1) |
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9.5.2 Gene therapy in dermatology |
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168 | (1) |
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9.6 Obstacles and ethical concerns |
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168 | (2) |
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9.6.1 Activation and delivery of gene |
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169 | (1) |
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9.6.2 Controlled gene expression |
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169 | (1) |
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9.6.3 Activation of immune response |
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169 | (1) |
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9.6.4 Improving efficiency of nuclease editing |
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169 | (1) |
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170 | (1) |
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9.7 Conclusions and future prospective |
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170 | (1) |
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170 | (1) |
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170 | (7) |
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10 Algae biotechnology for nutritional and pharmaceutical applications |
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177 | (18) |
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177 | (2) |
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179 | (3) |
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179 | (1) |
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179 | (2) |
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181 | (1) |
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181 | (1) |
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182 | (1) |
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182 | (1) |
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10.2.7 Additional nutrients |
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182 | (1) |
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182 | (2) |
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10.3.1 Dairy and probiotic products |
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184 | (1) |
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10.4 Pharmaceutical algae feature |
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184 | (6) |
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10.4.1 Antioxidant, antiinflammatory, and antimicrobial activities |
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184 | (5) |
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10.4.2 Antitherapy activity |
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189 | (1) |
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10.4.3 Microalgae anticancer property |
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190 | (1) |
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10.4.4 Anticancer properties of macroalgae |
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190 | (1) |
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190 | (1) |
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190 | (1) |
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191 | (1) |
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191 | (4) |
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11 Phage therapy: a promising approach to counter antimicrobial drug resistance |
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195 | (10) |
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11.1 Overview of antimicrobial drug resistance |
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195 | (1) |
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11.2 Phage therapy to counter antibacterial resistance |
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195 | (1) |
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11.3 Phages against antimicrobial resistance---an alternative strategy |
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196 | (1) |
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11.4 Mode of action of phage |
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196 | (1) |
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11.5 Journey of phage therapy |
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197 | (1) |
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11.6 Different approaches for phage therapy |
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198 | (1) |
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11.6.1 Single-phage therapy and polyphage therapy |
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198 | (1) |
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11.6.2 Phage combined with antibiotics |
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199 | (1) |
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11.6.3 Phage-derived enzymes as antimicrobials |
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199 | (1) |
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199 | (1) |
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11.7 Strategies and recent advances in phage therapy |
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199 | (1) |
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11.8 Options for the administration of phage therapy |
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200 | (1) |
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11.9 Real-time use of phage therapy |
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200 | (1) |
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11.10 Upside and flipside of phage therapy |
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200 | (1) |
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11.11 Regulatory requirements |
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201 | (1) |
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11.12 Outstanding challenges in phage therapy |
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202 | (1) |
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11.13 Conclusion and future directions |
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202 | (1) |
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202 | (1) |
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202 | (3) |
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12 Biotechnology strategies for the development of novel therapeutics and vaccines against the novel COVID-19 pandemic |
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205 | (22) |
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12.1 Antiviral COVID-19 drugs |
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205 | (4) |
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12.2 Monoclonal antibodies against COVID-19 |
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209 | (2) |
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12.3 Vaccines against COVID-19 |
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211 | (9) |
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12.3.1 Inactivated and attenuated viruses |
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211 | (4) |
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12.3.2 Protein-and peptide-based vaccines |
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215 | (2) |
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12.3.3 Viral vector-based vaccine |
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217 | (1) |
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12.3.4 DNA-based vaccines |
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218 | (1) |
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12.3.5 RNA-based vaccines |
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219 | (1) |
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220 | (1) |
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220 | (7) |
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13 Applications of microbial omics in healthcare |
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227 | (22) |
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13.1 Introduction to microbial omics |
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227 | (2) |
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13.1.1 Microbial omics approaches |
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227 | (1) |
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13.1.2 Microbial omics data types |
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228 | (1) |
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13.2 Phylogenomics: inferring evolutionary relationships between microorganisms |
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229 | (2) |
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229 | (1) |
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13.2.2 Microbial evolution |
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230 | (1) |
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13.2.3 Tools for microbial phylogenomic analysis |
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230 | (1) |
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13.3 Metagenomics: concepts in reconstructing genomes from metagenomes |
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231 | (2) |
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13.3.1 Significance of human microbiome |
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231 | (1) |
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13.3.2 Metagenomic analysis |
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232 | (1) |
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13.3.3 Phylogenetic analysis |
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232 | (1) |
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232 | (1) |
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13.4 Applications of microbial omics in diagnosis |
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233 | (3) |
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233 | (1) |
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13.4.2 Multilocus sequence typing |
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234 | (1) |
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13.4.3 Pulse-field gel electrophoresis |
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235 | (1) |
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235 | (1) |
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13.4.5 Next-generation sequencing |
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236 | (1) |
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13.4.6 Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry |
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236 | (1) |
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13.4.7 Protein as biomarkers |
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236 | (1) |
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13.5 Pan-genomics: comparative genomics in the era of omics data explosion |
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236 | (3) |
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13.5.1 Microbial pan-genome as tool to analyze pathogenic bacterial species |
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236 | (1) |
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13.5.2 Application of comparative microbial genomics and tools |
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237 | (1) |
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13.5.3 Comparative microbial genomics tools |
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238 | (1) |
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13.6 Therapeutic approaches employing microbial genomes and proteomes |
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239 | (2) |
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13.6.1 Drug target identification |
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239 | (1) |
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13.6.2 Vaccine development |
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240 | (1) |
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240 | (1) |
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241 | (1) |
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241 | (1) |
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241 | (8) |
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14 Artificial intelligence applied to healthcare and biotechnology |
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249 | (10) |
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249 | (1) |
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250 | (1) |
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14.3 Algorithms used in artificial intelligence applications |
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251 | (1) |
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14.4 Supervised and unsupervised classification methods |
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251 | (1) |
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14.5 Machine learning and deep learning |
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251 | (1) |
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14.6 Steps needed during the application of artificial intelligence |
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252 | (1) |
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14.6.1 Data preprocessing |
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252 | (1) |
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14.7 Analysis and interpretation of the data |
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252 | (1) |
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14.8 The need for validation |
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253 | (1) |
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14.9 Outliers, overfitting, and underfitting |
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254 | (1) |
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254 | (1) |
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14.11 The significance of the multidisciplinary approach |
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255 | (1) |
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14.12 Conclusion and future directions |
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255 | (1) |
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256 | (3) |
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15 Intellectual property rights in healthcare: an overview |
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259 | (6) |
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259 | (1) |
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15.2 Intellectual properties |
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260 | (1) |
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15.3 Rights protected under intellectual property laws |
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261 | (1) |
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15.4 Intellectual property right in healthcare |
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262 | (1) |
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263 | (1) |
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15.5 Chemical products and pharmaceutical drugs |
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263 | (1) |
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15.6 Healthcare information technology |
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263 | (1) |
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15.6.1 Medical and surgical methods |
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263 | (1) |
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15.6.2 Regenerative medicine |
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263 | (1) |
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15.7 Gene patents and personalized medicines |
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264 | (1) |
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15.8 Indian patent advanced search system |
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264 | (1) |
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15.9 Indian pharmaceutical industries and scope of patents |
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264 | (1) |
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15.10 Patent licensing and transfer of rights |
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265 | (1) |
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265 | (1) |
| References |
|
265 | (2) |
| Index |
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267 | |