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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 High‐throughput DNA sequencing – concepts and limitations
by Kircher, Martin and Kelso, Janet
BioEssays, ISSN 0265-9247, 06/2010, Volume 32, Issue 6, pp. 524 - 536
ABI/Life Technologies SOLiD | Helicos HeliScope | Sanger capillary sequencing | Illumina Genome Analyzer | Roche/454 GS FLX Titanium | Roche/454 GS FLX titanium | ABI/life technologies SOLiD | Illumina genome analyzer | Biochemistry & Molecular Biology | Biology | Life Sciences & Biomedicine - Other Topics | Life Sciences & Biomedicine | Science & Technology | Sequence Analysis, DNA - instrumentation | Sequence Analysis, DNA - methods | Biotechnology | Research | Nucleotide sequence | Innovations | Genomics | Deoxyribonucleic acid--DNA | Index Medicus
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3. Full Text Chemical Diagnostics
: From Bench to Bedside
by L.S. Tang, Nelson and Poon, Terence
2013, Topics in current chemistry, ISBN 9783642399411, Volume 336, 204
Clinical chemistry | Diagnosis, Laboratory
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4. Full Text Comparison of sequencing utility programs
by Aronesty, Erik
The open bioinformatics journal, ISSN 1875-0362, 2013, Volume 7, Issue 1, pp. 1 - 8
Clipping | Utilities | Illumina | Ngs and next-generation | Sequencing
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5. Full Text Using next-generation sequencing approaches to isolate simple sequence repeat (SSR) loci in the plant sciences
by Juan E. Zalapa and Hugo Cuevas and Huayu Zhu and Shawn Steffan and Douglas Senalik and Eric Zeldin and Brent McCown and Rebecca Harbut and Philipp Simon
American journal of botany, ISSN 0002-9122, 2/2012, Volume 99, Issue 2, pp. 193 - 208
Transcriptomes | Microsatellites | Technology | Genomics | Microsatellite repeats | Genetic loci | Genomes | Molecular Marker Development | Plants | Shotguns | Sequencing | microsatellites | next generation sequencing | cranberry | high‐throughput genotyping | 454 and Illumina sequencing | organelle SSR | Vaccinium macrocarpon | 454 and illumina sequencing | High-throughput genotyping | Next generation sequencing | Cranberry | Organelle SSR | Life Sciences & Biomedicine | Plant Sciences | Science & Technology | Computational Biology - methods | Transcriptome | DNA, Chloroplast - genetics | Databases, Genetic | Molecular Sequence Data | Genetic Loci | Genotyping Techniques | Polymorphism, Genetic | Vaccinium macrocarpon - genetics | DNA, Mitochondrial - genetics | Mitochondria - genetics | Base Sequence | Plastids - genetics | Sequence Analysis, DNA - methods | DNA, Plant - genetics | Microsatellite Repeats | Usage | Genetic aspects | Microsatellites (Genetics) | Research | Nucleotide sequencing | Cranberries | Methods | DNA sequencing | Genotype & phenotype | Genetic markers | Gene loci | Plant sciences | Flowers & plants | Index Medicus
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6. Full Text Massively Parallel Sequencing of Short Tandem Repeats—Population data and mixture analysis results for the PowerSeq™ system
by van der Gaag, Kristiaan J and de Leeuw, Rick H and Hoogenboom, Jerry and Patel, Jaynish and Storts, Douglas R and Laros, Jeroen F.J and de Knijff, Peter
Forensic science international : genetics, ISSN 1872-4973, 2016, Volume 24, pp. 86 - 96
Pathology | Next Generation Sequencing (NGS) | Forensic science | STR stutter | Short tandem repeat (STR) | TSSV | MiSeq | Promega | Massively Parallel Sequencing (MPS) | Sequence variants | PowerSeq | Bioinformatics | Illumina | fdstools | Mixture analysis | Genetics & Heredity | Life Sciences & Biomedicine | Medicine, Legal | Legal Medicine | Science & Technology | Africa, Central | Genetics, Population | Netherlands | Amelogenin - genetics | Humans | Asia, Western | High-Throughput Nucleotide Sequencing | Continental Population Groups - genetics | Sequence Analysis, DNA | Microsatellite Repeats | Index Medicus
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7. Full Text Detecting false‐positive signals in exome sequencing
by Fuentes Fajardo, Karin V and Adams, David and Mason, Christopher E and Sincan, Murat and Tifft, Cynthia and Toro, Camilo and Boerkoel, Cornelius F and Gahl, William and Markello, Thomas and NIH Undiagnosed Dis Program and NISC Comparative Sequencing and NISC Comparative Sequencing Program
Human mutation, ISSN 1059-7794, 04/2012, Volume 33, Issue 4, pp. 609 - 613
WES | SureSelect Human All Exon | next generation sequencing | Exome sequencing | inherited disease | alignment errors | genomics | sequencing errors | Illumina | false positives | Inherited disease | Genomics | Sequencing errors | False positives | Alignment errors | Next generation sequencing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | United States | Humans | Genetic Diseases, Inborn - genetics | False Positive Reactions | Loss of Heterozygosity | Exome | Genetic Variation | National Institutes of Health (U.S.) | Homozygote | Female | Polymorphism, Single Nucleotide | Mutation | Sequence Analysis, DNA - methods | Index Medicus | Sureselect Human All exon | Next Generation Sequencing
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8. Full Text Navigating the tip of the genomic iceberg: Next-generation sequencing for plant systematics
by Shannon C. K. Straub and Matthew Parks and Kevin Weitemier and Mark Fishbein and Richard C. Cronn and Aaron Liston
American journal of botany, ISSN 0002-9122, 2/2012, Volume 99, Issue 2, pp. 349 - 364
Chloroplasts | Genomics | Genes | Methods and Applications for Phylogenetic and Ecological Studies | Ribosomal DNA | Phylogenetics | Genomes | Libraries | Plants | Phylogeny | Sequencing | reference‐guided assembly | chloroplast content | plastome | low‐copy nuclear gene | ribosomal DNA cistron | plant systematics | Asclepias | Illumina | next‐generation sequencing | genome skimming | Plastome | Genome skimming | Next-generation sequencing | Reference-guided assembly | Ribosomal DNA cistron | Chloroplast content | Plant systematics | Low-copy nuclear gene | Life Sciences & Biomedicine | Plant Sciences | Science & Technology | Asclepias - classification | Genomic Library | Genetic Loci | Genome, Plant | Polymorphism, Genetic | Sequence Alignment | Computer Simulation | Plastids - genetics | Asclepias - genetics | Genome, Mitochondrial | Genomics - methods | Sequence Analysis, DNA - methods | DNA, Plant - genetics | DNA, Ribosomal - genetics | Nomenclature | Milkweed | Botany | Genetic aspects | Research | Nucleotide sequencing | Identification and classification | Methods | DNA sequencing | Flowers & plants | Deoxyribonucleic acid--DNA | Polymorphism | Index Medicus
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9. Full Text Unique, dual-indexed sequencing adapters with UMIs effectively eliminate index cross-talk and significantly improve sensitivity of massively parallel sequencing
by MacConaill, Laura E and Burns, Robert T and Nag, Anwesha and Coleman, Haley A and Slevin, Michael K and Giorda, Kristina and Light, Madelyn and Lai, Kevin and Jarosz, Mirna and McNeill, Matthew S and Ducar, Matthew D and Meyerson, Matthew and Thorner, Aaron R
BMC genomics, ISSN 1471-2164, 01/2018, Volume 19, Issue 1, pp. 30 - 30
Molecular barcode | Multiplexing | UMI | Massively parallel sequencing | Barcode cross-talk | Adapter | Index | Illumina | Next generation sequencing | Research | Nucleotide sequencing | Methods | Genetic screening | DNA sequencing | Multiprocessing | Usage | Analysis | Index Medicus
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