Direct selection of human genomic loci by microarray hybridization

Albert, Thomas J, Molla, Michael N, Muzny, Donna M, Nazareth, Lynne, Wheeler, David, Song, Xingzhi, Richmond, Todd A, Middle, Chris M +4 more·2007·Nature Methods

Cited by (682)

Items 501–600 of 682

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  5. Great expectations: using massively parallel sequencing to solve inherited disorders
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  7. Moving Towards Third‐Generation Sequencing Technologies
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  8. Development of genomic resources for ornamental lilies (Lilium L.)
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  9. Nested Patch PCR for Highly Multiplexed Amplification of Genomic Loci
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  10. Novel Sequencing-based Strategies for High-Throughput Discovery of Genetic Mutations Underlying Inherited Antibody Deficiency Disorders
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  11. Innovative technology for cancer risk analysis
    S. Tommas, Katia Danza, Brunella Pilato, Simona De Summa · 2011 · Annals of Oncology
  12. A Review of DNA Enrichment Technologies
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  13. Whole-exome sequencing and whole-genome sequencing
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  14. Low-cost and clinically applicable copy number profiling using repeat DNA
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  17. Copy number variation in the autism genome
    Lars Feuk · 2008 · Expert Opinion on Medical Diagnostics
  18. Translation of next-generation sequencing (NGS) into molecular diagnostics / Umsetzung von Next Generation Sequencing in der molekularen Diagnostik
    S. Kotschote, Carola L. Wagner, C. Marschall, K. Mayer, K. Hirv, M. Kerick, B. Timmermann, H. Klein · 2010 · Journal of Laboratory Medicine
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  26. Targeted Sequencing Strategies in Cancer Research
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  27. Next-generation Sequencing in Clinical Molecular Diagnostics
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  28. Polymorphism discovery in high-throughput resequenced microarray-enriched human genomic loci.
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    Joy D. Van Nostrand, Terry J. Gentry, Jizhong Z. Zhou · 2012 · Springer eBooks
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  38. Targeted Hybrid-Capture for Somatic Mutation Detection in the Clinic
    Catherine E. Cottrell, Andrew J. Bredemeyer, Hussam Al‐Kateb · 2014 · Elsevier eBooks
  39. Challenges in the Clinical Use of Genome Sequencing
    Robert C. Green, Heidi L. Rehm, Isaac S. Kohane · 2012
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    Tongming Yin · 2010 · Hereditas (Beijing)
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    Rodrigo Goya, Irmtraud M. Meyer, Marco A. Marra · 2011 · Springer eBooks
  45. Targeted Hybrid Capture Methods
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    Karl V. Voelkerding, Emily M. Coonrod, Jacob Durtschi, Rebecca L. Margraf · 2016 · Springer eBooks
  47. Nucleic Acids as Molecular Diagnostics
    A. Keller, E. Meese · 2014 · Wiley eBooks
  48. High-Throughput Sequencing of the Major Histocompatibility Complex following Targeted Sequence Capture
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  49. Wavelet Analysis in Current Cancer Genome to Identify Driver Mutation
    Saiba Najeeb, Nijil Raj N · 2018
  50. The Evolution of DNA Sequencing in Pharmacogenomics
    S. Scherer · 2019 · Advances in Molecular Pathology
  51. Implementation of Exome Sequencing Assay
    Samya Chakravorty, Arunkanth Ankala, Madhuri Hegde · 2018 · Springer eBooks
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    Qiongqiong Xu, Xiaodong Zheng, Yiwen Mao, Weiwei Chen, Shirui Chen, Hui Zhang, Qi Zhen, Bao Li, Yong Liang, Huiyao Ge et al. · 2022 · Molecular Genetics & Genomic Medicine
  53. DNA Fragment Enrichment for High-Throughput Sequencing
    Alexander N. Sinyakov, Elena V. Kostina · 2023 · Molecular Biology
  54. Genomics and Cancer Risk Assessment
    Michal R. Schweiger, Bernd Timmermann · 2011
  55. Targeted Capture and Massively Parallel Sequencing in Pediatric Cardiomyopathy: Development of Novel Diagnostics
    Muhammad Tariq, Thanh-Tam Le, Patrick P. Putnam, Steven J. Kindel, Mehdi A. Keddache, Stephanie M. Ware · 2012 · Cardiogenetics
  56. Solution-Phase Exome Capture
    Elaine R. Mardis, William Richard McCombie · 2016 · Cold Spring Harbor Protocols
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    Alba Sanchis Juan · 2019
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    Ulrika Gunnarsson · 2009 · Uppsala University Publications (Uppsala University)
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    Kristian Ovaska · 2014 · Työväentutkimus Vuosikirja
  62. Mutation Detection in Plants by Enzymatic Mismatch Cleavage
    Bradley John Till · 2010
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    Judith Necker · 2008 · edoc (University of Basel)
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  74. Sequencing Strategies and Tactics in DNA and RNA Analysis
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  81. Methods to Prepare DNA for Efficient Massive Sequencing
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  85. Optimized Probe Selection for Pan-genomic DNA Microarrays
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  86. PHG Foundation project team and authors
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  87. Whole-Exome Sequencing of Patients with Severe Disorders of Insulin Action
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  88. Sequence Alignment, Analysis, and Bioinformatic Pipelines
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  89. DEVELOPING NEW TOOLS FOR DETECTING GERMLINE
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  90. Using exome sequencing to study adaptive evolution in non-human primates and human populations
    Renee D. George · 2012 · ResearchWorks at the University of Washington (University of Washington)
  91. Genetic dissection of the transcriptional hypoxia response and genomic regional capture for massively parallel sequencing
    Douglas W. Turnbull · 2008 · Scholars' Bank (University of Oregon)
  92. Application of classical and next generation sequencing techniques to gene discovery and diagnostics in neurogenetic disorders
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  93. Allele Re-sequencing Technologies
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