SuperSelective primer pairs for sensitive detection of rare somatic mutations

Código QR

SuperSelective primer pairs for sensitive detection of rare somatic mutations

Abstract SuperSelective primers, by virtue of their unique design, enable the selective exponential amplification of rare DNA fragments containing somatic mutations in the presence of abundant closely related wild-type DNA fragments. However, when a SuperSelective primer is used in conjunction with...

Descripción completa

Guardado en:

Detalles Bibliográficos
Autores principales:	Fred Russell Kramer, Diana Yaneth Vargas
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2021
Materias:	Medicine R Science Q
Acceso en línea:	https://doaj.org/article/43b039342e344c4eb3331baf1432c5c1
Etiquetas:	Agregar Etiqueta Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares

Superselective embolization in management of remnant renal moiety and vessels after radical nephrectomy in horseshoe kidney
por: Fahad Sheckley, et al.
Publicado: (2022)

Superselective intra-arterial melphalan therapy for newly diagnosed and refractory retinoblastoma: results from a single institution
por: Thampi S, et al.
Publicado: (2013)

Deep convolutional neural networks for accurate somatic mutation detection
por: Sayed Mohammad Ebrahim Sahraeian, et al.
Publicado: (2019)

Coherent somatic mutation in autoimmune disease.
por: Kenneth Andrew Ross
Publicado: (2014)

A Rare Complication of Stapled Hemorrhoidopexy: Giant Pelvic Hematoma Treated with Super-Selective Percutaneous Angioembolization
por: Francesco Ferrara, et al.
Publicado: (2018)

Confidence-based somatic mutation evaluation and prioritization.
por: Martin Löwer, et al.
Publicado: (2012)

Estimating cell depth from somatic mutations.
por: Adam Wasserstrom, et al.
Publicado: (2008)

Recurrent somatic mutations and low germline predisposition mutations in Korean ALL patients
por: Sang-Yong Shin, et al.
Publicado: (2021)

Allelic imbalance of somatic mutations in cancer genomes and transcriptomes
por: Je-Keun Rhee, et al.
Publicado: (2017)

SENSITIVE AND SELECTIVE EXTRACTION FREE ION-PAIR COMPLEXOMETRIC DETERMINATION OF DOMPERIDONE IN PHARMACEUTICALS AND IN SPIKED HUMAN URINE
por: ZENITA,O, et al.
Publicado: (2011)

Longitudinal detection of somatic mutations in saliva and plasma for the surveillance of oral squamous cell carcinomas.
por: Ying Cui, et al.
Publicado: (2021)

The use of technical replication for detection of low-level somatic mutations in next-generation sequencing
por: Junho Kim, et al.
Publicado: (2019)

High-throughput mutation profiling identifies frequent somatic mutations in advanced gastric adenocarcinoma.
por: Jeeyun Lee, et al.
Publicado: (2012)

Inherited determinants of early recurrent somatic mutations in prostate cancer
por: Alessandro Romanel, et al.
Publicado: (2017)

Somatic SF3B1 hotspot mutation in prolactinomas
por: Chuzhong Li, et al.
Publicado: (2020)

Systematic Review of Somatic Mutations in Splenic Marginal Zone Lymphoma
por: Carolina Jaramillo Oquendo, et al.
Publicado: (2019)

Differences between germline and somatic mutation rates in humans and mice
por: Brandon Milholland, et al.
Publicado: (2017)

The prognostic effects of somatic mutations in ER-positive breast cancer
por: Obi L. Griffith, et al.
Publicado: (2018)

Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types
por: Runjun D. Kumar, et al.
Publicado: (2017)

Using somatic variant richness to mine signals from rare variants in the cancer genome
por: Saptarshi Chakraborty, et al.
Publicado: (2019)

The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model
por: Katherine C. MacKenzie, et al.
Publicado: (2021)

Somatic activating mutations in MAP2K1 cause melorheostosis
por: Heeseog Kang, et al.
Publicado: (2018)

Typing tumors using pathways selected by somatic evolution
por: Sheng Wang, et al.
Publicado: (2018)

Orbital-selective pairing and superconductivity in iron selenides
por: Emilian M. Nica, et al.
Publicado: (2017)

Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESS
por: A. Rose Brannon, et al.
Publicado: (2021)

Sensitive detection of rare disease-associated cell subsets via representation learning
por: Eirini Arvaniti, et al.
Publicado: (2017)

The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes
por: Bernard Pereira, et al.
Publicado: (2016)

Urinary Exosomal and cell-free DNA Detects Somatic Mutation and Copy Number Alteration in Urothelial Carcinoma of Bladder
por: Dong Hyeon Lee, et al.
Publicado: (2018)

Composite synchronization on two pairs of vibrators in a far super-resonant vibrating system with the single rigid frame
por: Xueliang Zhang, et al.
Publicado: (2021)

Non-coding somatic mutations converge on the PAX8 pathway in ovarian cancer
por: Rosario I. Corona, et al.
Publicado: (2020)

Pancancer modelling predicts the context-specific impact of somatic mutations on transcriptional programs
por: Hatice U. Osmanbeyoglu, et al.
Publicado: (2017)

Germline MC1R status influences somatic mutation burden in melanoma
por: Carla Daniela Robles-Espinoza, et al.
Publicado: (2016)

Somatic mutations and single-cell transcriptomes reveal the root of malignant rhabdoid tumours
por: Lars Custers, et al.
Publicado: (2021)

Hierarchical tissue organization as a general mechanism to limit the accumulation of somatic mutations
por: Imre Derényi, et al.
Publicado: (2017)

Molecular classification of prostate adenocarcinoma by the integrated somatic mutation profiles and molecular network
por: Lei Yang, et al.
Publicado: (2017)

Author Correction: The prognostic effects of somatic mutations in ER-positive breast cancer
por: Obi L. Griffith, et al.
Publicado: (2018)

Somatic Trp53 mutations differentially drive breast cancer and evolution of metastases
por: Yun Zhang, et al.
Publicado: (2018)

Comparison and validation of some ITS primer pairs useful for fungal metabarcoding studies.
por: Michiel Op De Beeck, et al.
Publicado: (2014)

Erratum: The somatic mutation profiles of 2,433 breast cancers refine their genomic and transcriptomic landscapes
por: Bernard Pereira, et al.
Publicado: (2016)

Somatic Tumor Mutations Detected by Targeted Next Generation Sequencing in Minute Amounts of Serum-Derived Cell-Free DNA
por: Marjolein J. A. Weerts, et al.
Publicado: (2017)