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1. Next-Generation Sequencing
: Current Technologies and Applications
by Xu, Jianping (Professor of Biology), 1965- editor of compilation
2014, ISBN 1908230339, xi, 159
Science | Sequential analysis | Nucleotide sequence | Bioinformatics | Sequence alignment (Bioinformatics)
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2. Full Text Targeted Next‐Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics
by Sikkema‐Raddatz, Birgit and Johansson, Lennart F and Boer, Eddy N and Almomani, Rowida and Boven, Ludolf G and Berg, Maarten P and Spaendonck‐Zwarts, Karin Y and Tintelen, J. Peter and Sijmons, Rolf H and Jongbloed, Jan D. H and Sinke, Richard J
Human mutation, ISSN 1059-7794, 07/2013, Volume 34, Issue 7, pp. 1035 - 1042
guidelines | diagnostics | targeted NGS | next‐generation sequencing | Targeted NGS | Next-generation sequencing | Diagnostics | Guidelines | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Cardiomyopathy, Dilated - genetics | Cardiomyopathies - genetics | Reproducibility of Results | Exons | Humans | Sensitivity and Specificity | Cardiomyopathies - diagnosis | Cardiomyopathy, Dilated - diagnosis | Mutation | High-Throughput Nucleotide Sequencing - methods | Sequence Analysis, DNA - methods | Nucleotide sequencing | Diagnostic equipment (Medical) | Media coverage | DNA sequencing | Cardiomyopathy | Index Medicus
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3. Full Text ANGSD: Analysis of Next Generation Sequencing Data
by Korneliussen, Thorfinn Sand and Albrechtsen, Anders and Nielsen, Rasmus
BMC bioinformatics, ISSN 1471-2105, 11/2014, Volume 15, Issue 1, pp. 356 - 356
Association studies | Next-generation sequencing | Bioinformatics | Population genetics | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Biotechnology & Applied Microbiology | Biochemical Research Methods | Science & Technology | Mathematical & Computational Biology | Likelihood Functions | Genetics, Population - methods | Gene Frequency | Genotype | Polymorphism, Single Nucleotide | Software | High-Throughput Nucleotide Sequencing - methods | Genetic aspects | Nucleotide sequencing | Analysis | DNA sequencing | Genotype & phenotype | Genomes | C plus plus | Chromosomes | Index Medicus | Freeware | Format | Statistical analysis | Samples | Statistical methods | Source code | Statistics | Sequencing
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4. Full Text Ten years of next-generation sequencing technology
by van Dijk, Erwin L and Auger, Hélène and Jaszczyszyn, Yan and Thermes, Claude
Trends in genetics, ISSN 0168-9525, 2014, Volume 30, Issue 9, pp. 418 - 426
Medical Education | ChIP-seq | genomics | DNA-seq | RNA-seq | NGS library preparation | Next-generation sequencing (NGS) | Genomics | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Sequence Analysis, RNA | Humans | Translational Medical Research | Genome, Human | Genomics - methods | High-Throughput Nucleotide Sequencing - methods | Sequence Analysis, DNA | Information storage and retrieval | Index Medicus
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5. Full Text Next‐generation sequencing technologies for environmental DNA research
by SHOKRALLA, SHADI and SPALL, JENNIFER L and GIBSON, JOEL F and HAJIBABAEI, MEHRDAD
Molecular ecology, ISSN 0962-1083, 04/2012, Volume 21, Issue 8, pp. 1794 - 1805
environmental monitoring | environmental DNA | metagenomics | next‐generation sequencing | next-generation sequencing | DNA - genetics | Metagenomics | High-Throughput Nucleotide Sequencing - instrumentation | High-Throughput Nucleotide Sequencing - methods | DNA - analysis | Environmental Monitoring - methods | Genetic research | Environmental monitoring | Analysis | DNA | Genes | Molecular biology | Ecology | Deoxyribonucleic acid--DNA | Index Medicus
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6. Full Text Next‐generation TCR sequencing – a tool to understand T‐cell infiltration in human cancers
by Poschke, Isabel and Flossdorf, Michael and Offringa, Rienk
The Journal of pathology, ISSN 0022-3417, 12/2016, Volume 240, Issue 4, pp. 384 - 386
tumour‐infiltrating lymphocytes | T‐cell receptor repertoire | next‐generation sequencing | oesophageal cancer | T-cell receptor repertoire | next-generation sequencing | tumour-infiltrating lymphocytes | Pathology | Oncology | Life Sciences & Biomedicine | Science & Technology | United Kingdom | High-Throughput Nucleotide Sequencing | Lymphocytes, Tumor-Infiltrating | T-Lymphocytes | Humans | T cells | Squamous cell carcinoma | Index Medicus
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7. Full Text Next generation sequencing technology: Advances and applications
by Buermans, H.P.J and den Dunnen, J.T
Biochimica et biophysica acta. Molecular basis of disease, ISSN 0925-4439, 10/2014, Volume 1842, Issue 10, pp. 1932 - 1941
Basic technology | Single molecule sequencing | Nanopore | Applications | Next generation sequencing | Sequence by synthesis | Biochemistry & Molecular Biology | Biophysics | Life Sciences & Biomedicine | Science & Technology | Cell Biology | RNA | Genomics
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8. Full Text Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease
by Treff, Nathan R., Ph.D and Fedick, Anastasia, B.S and Tao, Xin, M.S and Devkota, Batsal, Ph.D and Taylor, Deanne, Ph.D and Scott, Richard T., M.D
Fertility and sterility, ISSN 0015-0282, 2013, Volume 99, Issue 5, pp. 1377 - 1384.e6
Internal Medicine | Obstetrics and Gynecology | Next-generation sequencing | preimplantation genetic diagnosis | monogenic disorder | aneuploidy screening | genotyping | Life Sciences & Biomedicine | Obstetrics & Gynecology | Reproductive Biology | Science & Technology | Predictive Value of Tests | Genetic Testing | Humans | Risk Factors | Genetic Diseases, Inborn - genetics | Aneuploidy | Blastocyst - physiology | Genotype | Male | Genetic Diseases, Inborn - epidemiology | Preimplantation Diagnosis - methods | Mutagenesis, Insertional - genetics | Pregnancy | Point Mutation - genetics | Lymphocytes - physiology | Fertilization in Vitro | Gene Deletion | Female | Genetic Diseases, Inborn - diagnosis | Genetic research | Medical colleges | Analysis | Index Medicus
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9. Full Text Next-generation sequencing: Impact of exome sequencing in characterizing Mendelian disorders
by Rabbani, Bahareh and Mahdieh, Nejat and Hosomichi, Kazuyoshi and Nakaoka, Hirofumi and Inoue, Ituro
Journal of human genetics, ISSN 1434-5161, 10/2012, Volume 57, Issue 10, pp. 621 - 632
mendelian disorder | mutation | exome sequencing | NGS | WES | next-generation sequencing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Genetic Diseases, Inborn - genetics | Databases, Genetic | DNA Mutational Analysis - methods | Genetic Testing - methods | Exome | Genetics, Population - methods | Pedigree | Polymorphism, Single Nucleotide | Genome, Human | Genetic Diseases, Inborn - diagnosis | Genetic Linkage | Heredity | Next-generation sequencing | Gene mapping | Genes | Linkage analysis | Index Medicus
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