205 results on '"Zhang, David Yu"'
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2. Rapid, tunable, and multiplexed detection of RNA using convective array PCR
3. Transfer Learning Of Gene Expression Using Reactome
4. Direct capture and sequencing reveal ultra-short single-stranded DNA in biofluids
5. Limitations and opportunities of technologies for the analysis of cell-free DNA in cancer diagnostics
6. Designing highly multiplex PCR primer sets with Simulated Annealing Design using Dimer Likelihood Estimation (SADDLE)
7. Ensemble of nucleic acid absolute quantitation modules for copy number variation detection and RNA profiling
8. Enhanced Detection of Novel Low‐Frequency Gene Fusions via High‐Yield Ligation and Multiplexed Enrichment Sequencing
9. Extended Enrichment for Ultrasensitive Detection of Low‐Frequency Mutations by Long Blocker Displacement Amplification
10. Gene Expression Reactomes Across Species Do Not Correlate with Gene Structural Similarity
11. Highly multiplexed rapid DNA detection with single-nucleotide specificity via convective PCR in a portable device
12. Selective multiplexed enrichment for the detection and quantitation of low-fraction DNA variants via low-depth sequencing
13. Microsatellite Instability Detection in Cancer: A Multiplex qPCR Approach that Obviates the Need for Matching Normal Samples.
14. High Frequency Longitudinal RNAseq Reveals Temporally Varying Genes and Recovery Trajectories in Rats
15. Microsatellite Instability Detection in Clinical Cancer Samples: A Multiplex qPCR Approach without Matching Normal Samples
16. Calibration-free NGS quantitation of mutations below 0.01% VAF
17. Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for rapid, accurate, and affordable somatic mutation detection
18. Confirming putative variants at ≤ 5% allele frequency using allele enrichment and Sanger sequencing
19. High sensitivity sanger sequencing detection of BRAF mutations in metastatic melanoma FFPE tissue specimens
20. A deep learning model for predicting next-generation sequencing depth from DNA sequence
21. Metastable hybridization-based DNA information storage to allow rapid and permanent erasure
22. A Novel NGS Assay to Detect Any KMT2A fusion Transcript at Low Levels
23. Multiplexed enrichment of rare DNA variants via sequence-selective and temperature-robust amplification
24. DNA-Based Fixed Gain Amplifiers and Linear Classifier Circuits
25. Towards Domain-Based Sequence Design for DNA Strand Displacement Reactions
26. Highly Sensitive Blocker Displacement Amplification for Detection of Low-Level JAK2V617F Variant.
27. Hairpin Structure Facilitates Multiplex High-Fidelity DNA Amplification in Real-Time Polymerase Chain Reaction
28. Cost-Efficient Sequence-Based Nonextensible Oligonucleotide in Real-Time PCR and High-Throughput Sequencing
29. eP042: Highly sensitive blocker displacement amplification-based qPCR approach in detecting low level JAK2 variant
30. Highly Sensitive Blocker Displacement Amplification for Detection of Low-Level JAK2V617FVariant
31. Engineering Entropy-Driven Reactions and Networks Catalyzed by DNA
32. Enzyme-Free Nucleic Acid Logic Circuits
33. Single-Tube qPCR Detection and Quantitation of Hotspot Mutations Down to 0.01% Variant Allele Fraction
34. Hairpin structure facilitates high-fidelity DNA amplification reactions in both qPCR and high-throughput sequencing
35. Direct capture and sequencing reveal ultra-short single-stranded DNA in biofluids
36. Single Tube qPCR detection and quantitation of hotspot mutations down to 0.01% VAF
37. Predicting stability of DNA bulge at mononucleotide microsatellite
38. High-throughput variant detection using a color-mixing strategy
39. Publisher Correction: Multiplexed enrichment of rare DNA variants via sequence-selective and temperature-robust amplification
40. Additional file 6 of Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for rapid, accurate, and affordable somatic mutation detection
41. High-Throughput Measurement of Metastable DNA Secondary Structures using Multiplexed Low-Yield Bisulfite Sequencing (MLB-seq)
42. Error suppression mechanisms for DNA tile self-assembly and their simulation
43. Confirming Putative Variants at ≤5% Allele Frequency Using Allele Enrichment and Sanger Sequencing
44. Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for Rapid, Accurate, and Affordable Somatic Mutation Detection
45. Single-Tube qPCR Detection and Quantitation of Hotspot Mutations Down to 0.01% Variant Allele Fraction.
46. Abstract 5891: Plasma-based BDA-NGS test holds potential in circulating nucleic acid based oncogenic aberration detection
47. High-throughput methods for measuring DNA thermodynamics
48. Nucleic Acid Quantitation with Log–Linear Response Hybridization Probe Sets
49. Detecting and Quantitating Low Fraction DNA Variants with Low-Depth Sequencing
50. Encoding multiple digital DNA signals in a single analog channel
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