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2014, ISBN 1908230339, xi, 159
Book
2.
Full Text
Targeted Next‐Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics
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
Journal Article
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
Journal Article
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
Journal Article
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
Journal Article
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Next‐generation TCR sequencing – a tool to understand T‐cell infiltration in human cancers
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
Journal Article
Biochimica et biophysica acta. Molecular basis of disease, ISSN 0925-4439, 10/2014, Volume 1842, Issue 10, pp. 1932 - 1941
Journal Article
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
Journal Article
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
Journal Article