| scholarly article | Q13442814 |
| P50 | author | Yibin Liu | Q63443283 |
| P2093 | author name string | Chen Song | |
| Matthew H Kulke | |||
| G Mike Makrigiorgos | |||
| Harvey Mamon | |||
| Alexander Makrigiorgos | |||
| Rachel Fontana | |||
| P2860 | cites work | An integrated map of genetic variation from 1,092 human genomes | Q22122153 |
| Emergence of KRAS mutations and acquired resistance to anti-EGFR therapy in colorectal cancer | Q24604601 | ||
| Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS) | Q24635921 | ||
| Two-round coamplification at lower denaturation temperature-PCR (COLD-PCR)-based sanger sequencing identifies a novel spectrum of low-level mutations in lung adenocarcinoma | Q24649847 | ||
| PCR-based methods for the enrichment of minority alleles and mutations | Q24657701 | ||
| A novel method for SNP detection using a new duplex-specific nuclease from crab hepatopancreas | Q24682065 | ||
| Digital PCR | Q24685020 | ||
| EGFR mutation and resistance of non-small-cell lung cancer to gefitinib | Q27824829 | ||
| Circulating mutant DNA to assess tumor dynamics | Q28289337 | ||
| Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing | Q29614576 | ||
| Detection of circulating tumor DNA in early- and late-stage human malignancies | Q29615778 | ||
| Rapid and sensitive detection of KRAS mutation after fast-COLD-PCR enrichment and high-resolution melting analysis. | Q54375389 | ||
| Antiprimer quenching-based real-time PCR and its application to the analysis of clinical cancer samples. | Q54618468 | ||
| Quantification of random genomic mutations. | Q54674731 | ||
| Sensitivity and specificity of single-nucleotide polymorphism scanning by high-resolution melting analysis. | Q54706020 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Detection and quantification of rare mutations with massively parallel sequencing | Q30472217 | ||
| Detection of tumor mutations in the presence of excess amounts of normal DNA. | Q30804424 | ||
| An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. | Q33590850 | ||
| Random Mutagenesis by Error-Prone PCR | Q33647024 | ||
| COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing | Q34109720 | ||
| Detection and quantification of mutations in the plasma of patients with colorectal tumors | Q34132363 | ||
| A decade's perspective on DNA sequencing technology | Q34163657 | ||
| Noninvasive identification and monitoring of cancer mutations by targeted deep sequencing of plasma DNA. | Q34278191 | ||
| Detection of ultra-rare mutations by next-generation sequencing | Q34291814 | ||
| High-throughput DNA sequencing errors are reduced by orders of magnitude using circle sequencing | Q34385801 | ||
| Depletion of Abundant Sequences by Hybridization (DASH): using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications. | Q34516997 | ||
| BEAMing: single-molecule PCR on microparticles in water-in-oil emulsions | Q34540801 | ||
| Full COLD-PCR protocol for noninvasive prenatal diagnosis of genetic diseases | Q34581056 | ||
| NRAS mutations with low allele burden have independent prognostic significance for patients with lower risk myelodysplastic syndromes | Q34740986 | ||
| Replacing PCR with COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing | Q34769683 | ||
| Universal noninvasive detection of solid organ transplant rejection | Q34794715 | ||
| COLD-PCR: a new platform for highly improved mutation detection in cancer and genetic testing | Q34963648 | ||
| Clinical validation of the detection of KRAS and BRAF mutations from circulating tumor DNA. | Q35127938 | ||
| Restriction endonuclease-mediated selective polymerase chain reaction: a novel assay for the detection of K-ras mutations in clinical samples | Q35753312 | ||
| DNA bar coding and pyrosequencing to identify rare HIV drug resistance mutations | Q35916998 | ||
| Ultrasensitive measurement of hotspot mutations in tumor DNA in blood using error-suppressed multiplexed deep sequencing. | Q36185551 | ||
| Differential strand separation at critical temperature: a minimally disruptive enrichment method for low-abundance unknown DNA mutations | Q36580836 | ||
| Targeted single molecule mutation detection with massively parallel sequencing | Q36588964 | ||
| The expanding scope of DNA sequencing | Q38058682 | ||
| Detecting colorectal cancer in stool with the use of multiple genetic targets | Q39569642 | ||
| FLAG assay as a novel method for real-time signal generation during PCR: application to detection and genotyping of KRAS codon 12 mutations | Q40068805 | ||
| Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers | Q40538213 | ||
| Continuously tunable nucleic acid hybridization probes | Q43146556 | ||
| Restriction site mutation analysis, a proposed methodology for the detection and study of DNA base changes following mutagen exposure | Q46580075 | ||
| Mutant DNA in plasma of lung cancer patients: potential for monitoring response to therapy | Q46743042 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial 4.0 International | Q34179348 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 19 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e146 | |
| P577 | publication date | 2016-07-18 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | Elimination of unaltered DNA in mixed clinical samples via nuclease-assisted minor-allele enrichment | |
| P478 | volume | 44 |
| Q90621936 | A nuclease-polymerase chain reaction enables amplification of probes used for capture-based DNA target enrichment |
| Q39094514 | COLD-PCR Technologies in the Area of Personalized Medicine: Methodology and Applications. |
| Q47162594 | CUT-PCR: CRISPR-mediated, ultrasensitive detection of target DNA using PCR. |
| Q57053765 | Denaturation-Enhanced Droplet Digital PCR for Liquid Biopsies |
| Q53836887 | Detecting Rare Mutations and DNA Damage with Sequencing-Based Methods. |
| Q50059462 | Early Assessment of Lung Cancer Immunotherapy Response via Circulating Tumor DNA. |
| Q88319839 | Enhanced detection of microsatellite instability using pre-PCR elimination of wild-type DNA homo-polymers in tissue and liquid biopsies |
| Q90467894 | Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia |
| Q91902392 | Highly specific enrichment of rare nucleic acid fractions using Thermus thermophilus argonaute with applications in cancer diagnostics |
| Q92243259 | Imaging phenotype using radiomics to predict dry pleural dissemination in non-small cell lung cancer |
| Q39149201 | Liquid biopsies come of age: towards implementation of circulating tumour DNA. |
| Q33557917 | Methylation-sensitive enrichment of minor DNA alleles using a double-strand DNA-specific nuclease |
| Q40483796 | Multiplexed Elimination of Wild-Type DNA and High-Resolution Melting Prior to Targeted Resequencing of Liquid Biopsies |
| Q56688655 | Multiplexed enrichment of rare DNA variants via sequence-selective and temperature-robust amplification |
| Q90187687 | Nuclease-Assisted Minor Allele Enrichment Using Overlapping Probes-Assisted Amplification-Refractory Mutation System: An Approach for the Improvement of Amplification-Refractory Mutation System-Polymerase Chain Reaction Specificity in Liquid Biopsie |
| Q100533805 | PIK3CA mutation enrichment and quantitation from blood and tissue |
| Q47822530 | Somatic Mutations Drive Distinct Imaging Phenotypes in Lung Cancer. |
| Q28066706 | Technological considerations for genome-guided diagnosis and management of cancer |
Search more.