148 results on '"Zhang, David Yu"'
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2. Screening hydrogels for antifibrotic properties by implanting cellularly barcoded alginates in mice and a non-human primate
3. Direct capture and sequencing reveal ultra-short single-stranded DNA in biofluids
4. Limitations and opportunities of technologies for the analysis of cell-free DNA in cancer diagnostics
5. Designing highly multiplex PCR primer sets with Simulated Annealing Design using Dimer Likelihood Estimation (SADDLE)
6. Ensemble of nucleic acid absolute quantitation modules for copy number variation detection and RNA profiling
7. Transfer Learning Of Gene Expression Using Reactome
8. Enhanced Detection of Novel Low‐Frequency Gene Fusions via High‐Yield Ligation and Multiplexed Enrichment Sequencing
9. Highly multiplexed rapid DNA detection with single-nucleotide specificity via convective PCR in a portable device
10. Selective multiplexed enrichment for the detection and quantitation of low-fraction DNA variants via low-depth sequencing
11. Microsatellite Instability Detection in Cancer: A Multiplex qPCR Approach that Obviates the Need for Matching Normal Samples.
12. Extended Enrichment for Ultrasensitive Detection of Low‐Frequency Mutations by Long Blocker Displacement Amplification
13. Gene Expression Reactomes Across Species Do Not Correlate with Gene Structural Similarity
14. Calibration-free NGS quantitation of mutations below 0.01% VAF
15. Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for rapid, accurate, and affordable somatic mutation detection
16. Confirming putative variants at ≤ 5% allele frequency using allele enrichment and Sanger sequencing
17. High sensitivity sanger sequencing detection of BRAF mutations in metastatic melanoma FFPE tissue specimens
18. A deep learning model for predicting next-generation sequencing depth from DNA sequence
19. High Frequency Longitudinal RNAseq Reveals Temporally Varying Genes and Recovery Trajectories in Rats
20. Microsatellite Instability Detection in Clinical Cancer Samples: A Multiplex qPCR Approach without Matching Normal Samples
21. Metastable hybridization-based DNA information storage to allow rapid and permanent erasure
22. Multiplexed enrichment of rare DNA variants via sequence-selective and temperature-robust amplification
23. A Novel NGS Assay to Detect Any KMT2A fusion Transcript at Low Levels
24. Hairpin Structure Facilitates Multiplex High-Fidelity DNA Amplification in Real-Time Polymerase Chain Reaction
25. Highly Sensitive Blocker Displacement Amplification for Detection of Low-Level JAK2V617F Variant.
26. Cost-Efficient Sequence-Based Nonextensible Oligonucleotide in Real-Time PCR and High-Throughput Sequencing
27. eP042: Highly sensitive blocker displacement amplification-based qPCR approach in detecting low level JAK2 variant
28. Single-Tube qPCR Detection and Quantitation of Hotspot Mutations Down to 0.01% Variant Allele Fraction
29. Hairpin structure facilitates high-fidelity DNA amplification reactions in both qPCR and high-throughput sequencing
30. Highly Sensitive Blocker Displacement Amplification for Detection of Low-Level JAK2V617FVariant
31. Publisher Correction: Multiplexed enrichment of rare DNA variants via sequence-selective and temperature-robust amplification
32. Direct capture and sequencing reveal ultra-short single-stranded DNA in biofluids
33. Single Tube qPCR detection and quantitation of hotspot mutations down to 0.01% VAF
34. Predicting stability of DNA bulge at mononucleotide microsatellite
35. High-throughput variant detection using a color-mixing strategy
36. Additional file 6 of Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for rapid, accurate, and affordable somatic mutation detection
37. High-Throughput Measurement of Metastable DNA Secondary Structures using Multiplexed Low-Yield Bisulfite Sequencing (MLB-seq)
38. Confirming Putative Variants at ≤5% Allele Frequency Using Allele Enrichment and Sanger Sequencing
39. Oncogene Concatenated Enriched Amplicon Nanopore Sequencing for Rapid, Accurate, and Affordable Somatic Mutation Detection
40. Abstract 5891: Plasma-based BDA-NGS test holds potential in circulating nucleic acid based oncogenic aberration detection
41. High-throughput methods for measuring DNA thermodynamics
42. Nucleic Acid Quantitation with Log–Linear Response Hybridization Probe Sets
43. Detecting and Quantitating Low Fraction DNA Variants with Low-Depth Sequencing
44. Encoding multiple digital DNA signals in a single analog channel
45. Donut PCR: a rapid, portable, multiplexed, and quantitative DNA detection platform with single-nucleotide specificity
46. Single-Tube qPCR Detection and Quantitation of Hotspot Mutations Down to 0.01% Variant Allele Fraction.
47. A Novel NGS Assay to Detect Any KMT2Afusion Transcript at Low Levels
48. Simultaneous and stoichiometric purification of hundreds of oligonucleotides
49. Predicting DNA hybridization kinetics from sequence
50. Modular probes for enriching and detecting complex nucleic acid sequences
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