Direct selection of human genomic loci by microarray hybridization

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Items 301–400 of 682

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2. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders
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3. Photolithographic Synthesis of High-Density DNA and RNA Arrays on Flexible, Transparent, and Easily Subdivided Plastic Substrates
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5. Reduced-representation methylation mapping
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6. The LuWD40-1 Gene Encoding WD Repeat Protein Regulates Growth and Pollen Viability in Flax (Linum Usitatissimum L.)
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7. Next-Generation Mapping of Complex Traits with Phenotype-Based Selection and Introgression
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8. Finishing the finished human chromosome 22 sequence
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10. Gene Saturation: An Approach to Assess Exploration Stage of Gene Interaction Networks
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11. Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly
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12. High-throughput sequencing of microdissected chromosomal regions
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13. Next Generation Sequencing in the Clinical Domain: Clinical Advantages, Practical, and Ethical Challenges
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14. Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse
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15. Design and development of exome capture sequencing for the domestic pig (Sus scrofa)
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16. Target enrichment improves phylogenetic resolution in the genus Zanthoxylum (Rutaceae) and indicates both incomplete lineage sorting and hybridization events
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17. Efficient oligonucleotide probe selection for pan-genomic tiling arrays
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18. Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing
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19. Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer
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20. A probabilistic approach for SNP discovery in high-throughput human resequencing data
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21. Physical and Chemicals Mutagenesis in Plant Breeding
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22. Chromosome genomics uncovers plant genome organization and function
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23. PhylOPDb: a 16S rRNA oligonucleotide probe database for prokaryotic identification
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24. Mendelian, Non-Mendelian, Multigenic Inheritance, and Epigenetics
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25. Developmental Genetics and New Sequencing Technologies: The Rise of Nonmodel Organisms
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26. Practical, ethical and regulatory considerations for the evolving medical and research genomics landscape
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27. Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing
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28. Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing
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29. New technologies in the genetic approach to sudden cardiac death in the young
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30. Sequence Capture and Next-Generation Resequencing of Multiple Tagged Nucleic Acid Samples for Mutation Screening of Urea Cycle Disorders
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31. Capturing Darwin's dream
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32. Genomic sequence capture of haemosporidian parasites: Methods and prospects for enhanced study of host–parasite evolution
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33. Capturing prokaryotic dark matter genomes
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34. Clinical Versus Research Sequencing
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35. Targeted sequencing of the human X chromosome exome
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36. A bioinformatic platform to integrate target capture and whole genome sequences of various read depths for phylogenomics
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37. Advances in sarcoma molecular diagnostics
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38. Benefits and Limits of Phasing Alleles for Network Inference of Allopolyploid Complexes
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39. SNP Discovery by Transcriptome Pyrosequencing
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40. Next-generation sequencing approaches for genetic mapping of complex diseases
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41. Sequence capture and massively parallel sequencing to detect mutations associated with malignant hyperthermia
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42. Auditory and Vestibular Research
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43. Sequence capture across large phylogenetic scales by using pooled PCR‐generated baits: A case study of Lepidoptera
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44. Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing
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45. Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing
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46. Aiming off the target: recycling target capture sequencing reads for investigating repetitive DNA
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47. 161st ENMC International Workshop on nemaline myopathy and related disorders, Newcastle upon Tyne, 2008
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48. Bisulfite Methylation Profiling of Large Genomes
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49. The evolving role of next generation sequencing in myelodysplastic syndromes
    Travis P. Spaulding, Shannon Somer Stockton, Michael Robert Savona · 2019 · British Journal of Haematology
50. Fine Mapping of Quantitative Trait Loci on Bovine Chromosome 6 Affecting Calving Difficulty
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51. Multiplex target capture with double-stranded DNA probes
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52. Sanger Sequencing Principles, History, and Landmarks
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53. Solution-based targeted genomic enrichment for precious DNA samples
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54. Genomic medicine and neurological disease
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55. Dynamic Magnetic Nanomixers for Improved Microarray Assays by Eliminating Diffusion Limitation
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56. Maximizing Ion-Tagged Oligonucleotide Loading on Magnetic Ionic Liquid Supports for the Sequence-Specific Extraction of Nucleic Acids
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57. Whole human exome capture for high-throughput sequencing
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58. Adult Genetic Risk Screening
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59. Targeted sequencing with microfluidics
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60. Detection of Genomic Variation by Selection of a 9 Mb DNA Region and High Throughput Sequencing
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61. A comparison of whole genome sequencing with exome sequencing for family-based association studies
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62. Sequencing by Cyclic Ligation and Cleavage (CycLiC) directly on a microarray captured template
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63. A regression model for estimating DNA copy number applied to capture sequencing data
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64. Target enrichment sequencing in cultivated peanut (Arachis hypogaea L.) using probes designed from transcript sequences
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65. Next‐generation sequencing approaches in genetic rodent model systems to study functional effects of human genetic variation
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66. Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis
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67. Genomics and epigenomics: new promises of personalized medicine for cancer patients
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68. Enrichment of low abundance DNA/RNA by oligonucleotide-clicked iron oxide nanoparticles
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69. What we have learned from the next-generation sequencing: Contributions to the genetic diagnoses and understanding of pathomechanisms of neurodegenerative diseases
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70. Reliable resequencing of the human dystrophin locus by universal long polymerase chain reaction and massive pyrosequencing.
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71. Targeted Enrichment of Specific Regions in the Human Genome by Array Hybridization
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72. The Promise and Practicality of Population Genomics Research with Endangered Species
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73. Clinical genomics: from a truly personal genome viewpoint
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74. Development of Target Sequence Capture and Estimation of Genomic Relatedness in a Mixed Oak Stand
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75. Genetics of Chronic Obstructive Pulmonary Disease: A Succinct Review, Future Avenues and Prospective Clinical Applications
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76. Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals
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77. ConcatSeq: A method for increasing throughput of single molecule sequencing by concatenating short DNA fragments
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78. Next generation sequencing in cardiomyopathy: towards personalized genomics and medicine
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79. Combining Microarray‐based Genomic Selection (MGS) with the Illumina Genome Analyzer Platform to Sequence Diploid Target Regions
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80. Empirical Evaluation of Oligonucleotide Probe Selection for DNA Microarrays
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81. Current status and future possibilities of molecular genetics techniques in Brassica napus
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82. Identification of Causal Sequence Variants of Disease in the Next Generation Sequencing Era
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83. Evolutionary history of Methyltransferase 1 genes in hexaploid wheat
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84. LIFE‐Seq: a universal L arge I ntegrated DNA F ragment E nrichment Seq uencing strategy for deciphering the transgene integration of genetically modified organisms
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85. Rapid and highly-specific generation of targeted DNA sequencing libraries enabled by linking capture probes with universal primers
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86. Increasing the specificity and function of DNA microarrays by processing arrays at different stringencies
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87. An improved understanding of cancer genomics through massively parallel sequencing.
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88. Identifying markers for resistance to sugarcane orange rust (Puccinia kuehnii) via selective genotyping and capture sequencing
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89. Sequencing Genomes: From Individuals to Populations
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90. Applications of Microarrays for Crop Improvement: Here, There, and Everywhere
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91. NewtCap : An Efficient Target Capture Approach to Boost Genomic Studies in Salamandridae (True Salamanders and Newts)
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92. A massive parallel sequencing workflow for diagnostic genetic testing of mismatch repair genes
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93. microDuMIP: target-enrichment technique for microarray-based duplex molecular inversion probes
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94. The Role and Future Possibilities of Next-Generation Sequencing in Studying Microbial Diversity
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95. Impact of Mendelian Inheritance in Cardiovascular Disease
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96. Targeted deep resequencing of the human cancer genome using next-generation technologies
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97. A Comprehensive Genetic Analysis of Candidate Genes Regulating Response to Trypanosoma congolense Infection in Mice
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100. Concurrent typing of over 4000 samples by long-range PCR amplicon-based NGS and rSSO revealed the need to verify NGS typing for HLA allelic dropouts
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