Direct selection of human genomic loci by microarray hybridization

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9. IFRD1 Is a Candidate Gene for SMNA on Chromosome 7q22-q23
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15. Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing
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21. Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing
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22. Detecting unknown sequences with DNA microarrays: explorative probe design strategies
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23. DNA Sequence Capture and Next-Generation Sequencing for the Molecular Diagnosis of Genetic Cardiomyopathies
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24. Enrichment of genomic DNA for polymorphism detection in a non‐model highly polyploid crop plant
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25. CRISPR-based enrichment strategies for targeted sequencing
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26. Photoelectrochemical synthesis of DNA microarrays
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27. Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure
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28. Clinical Genome Sequencing
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29. Multiplex Target Enrichment Using DNA Indexing for Ultra-High Throughput SNP Detection
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30. Identification of factors required for meristem function in Arabidopsis using a novel next generation sequencing fast forward genetics approach
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31. Comparative Population Genomics of the Ejaculate in Humans and the Great Apes
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32. Cracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and Perspectives
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33. Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing
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34. Genomic DNA Enrichment Using Sequence Capture Microarrays: a Novel Approach to Discover Sequence Nucleotide Polymorphisms (SNP) in Brassica napus L
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35. Reduced representation approaches to interrogate genome diversity in large repetitive plant genomes
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36. Express photolithographic DNA microarray synthesis with optimized chemistry and high-efficiency photolabile groups
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37. Calling SNPs without a reference sequence
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38. PrimerPooler: automated primer pooling to prepare library for targeted sequencing
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39. Targeted High-Throughput DNA Sequencing for Gene Discovery in Retinitis Pigmentosa
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40. A Low-Cost Exon Capture Method Suitable for Large-Scale Screening of Genetic Deafness by the Massively-Parallel Sequencing Approach
    Wenxue Tang, Dong Qian, Shoeb Ahmad, Douglas E. Mattox, Norman Wendell Todd, Harrison Han, Shouting Huang, Yuhua Li, Yunfeng Wang, Huawei Li et al. · 2012 · Genetic Testing and Molecular Biomarkers
41. Efficient targeted resequencing of human germline and cancer genomes by oligonucleotide-selective sequencing
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42. Microfluidic droplet enrichment for targeted sequencing
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43. Perspectives of DNA microarray and next-generation DNA sequencing technologies
    XiaoKun Teng, Huasheng Xiao · 2009 · Science in China Series C Life Sciences
44. Applying next-generation sequencing to pancreatic cancer treatment
    Elaine R. Mardis · 2012 · Nature Reviews Gastroenterology & Hepatology
45. Practical Tools to Implement Massive Parallel Pyrosequencing of PCR Products in Next Generation Molecular Diagnostics
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46. Genomic Sequencing for Cancer Diagnosis and Therapy
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47. Development of a Diagnostic Genetic Test for Simplex and Autosomal Recessive Retinitis Pigmentosa
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48. A novel approach for multi-domain and multi-gene family identification provides insights into evolutionary dynamics of disease resistance genes in core eudicot plants
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49. Whole genome sequencing for quantifying germline mutation frequency in humans and model species: cautious optimism.
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50. Captured metagenomics: large-scale targeting of genes based on ‘sequence capture’ reveals functional diversity in soils
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51. Microfluidics for genome-wide studies involving next generation sequencing
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52. Enrichment of super-sized resequencing targets from the human genome
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53. TILLING for Mutations in Model Plants and Crops
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54. Recent advances in coeliac disease genetics: Figure 1
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55. Targeted Capture of Homoeologous Coding and Noncoding Sequence in Polyploid Cotton
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56. Targeted resequencing of the microRNAome and 3′UTRome reveals functional germline DNA variants with altered prevalence in epithelial ovarian cancer
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57. Programmable and Highly Resolved In Vitro Detection of 5‐Methylcytosine by TALEs
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58. Targeted next-generation sequencing of DNA regions proximal to a conserved GXGXXG signaling motif enables systematic discovery of tyrosine kinase fusions in cancer
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59. Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals
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60. Informatics and clinical genome sequencing: opening the black box
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61. DNA methylation profiling in cancer
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62. Species tree estimation of North American chorus frogs (Hylidae: Pseudacris) with parallel tagged amplicon sequencing
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63. GC-Biased Evolution Near Human Accelerated Regions
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66. Reduced Representation Methods for Subgenomic Enrichment and Next-Generation Sequencing
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67. CRISPR-Cap: multiplexed double-stranded DNA enrichment based on the CRISPR system
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68. Targeted capture of complete coding regions across divergent species
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70. Large‐scale genomic analysis of ovarian carcinomas
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82. Application of large-scale sequencing to marker discovery in plants
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89. Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
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