English Español

Inicio
Pruebas
Productos
Empresas
Tecnologías
Temas
Insights
Guía del comprador
Socios

Inicio
Pruebas
Productos
Empresas
Tecnologías
Temas
Insights
Guía del comprador
Socios

English Español

Loading

Loading

IVDmap

Plataforma global para descubrimiento de productos, mapeo de proveedores y soporte a decisiones de compra.

Plataforma

Inicio
Productos
Empresas
Tecnologías
Insights
Herramientas
Glosario

Compradores

Guía del comprador
Paquetes de recursos
Solicitar cotización
Casos de estudio

Socios

Ser socio
Cooperación OEM
Solicitud de colaboración

Empresa / Información legal

Contacto
Privacidad
Condiciones
Aviso legal
[email protected]

Aviso regulatorio Aviso legal Privacidad CondicionesSolo para uso profesional. La disponibilidad varía según el país.

Buscar en IVDmap

Busque productos, empresas, pruebas y guías: pase de la consulta a la solicitud de cotización en un solo lugar.

Buscar

Mostrando 1 - 12 de 16 para «Variant Allele Frequency»

Todos los resultados (16)Artículo (16)

Artículo

A next-generation sequencing-based pharmacogenetic study of ABCB1, ABCC1, and ABCC2 variants associated with antiseizure medication response in Turkish epilepsy patients.

Research record from Epileptic Disord, 2026-09-05. PMID 42700104.

Artículo

A novel multiplex digital PCR assay for simultaneous quantification of androgen receptor amplification, mutations, and splice variants in cell-free nucleic acids from metastatic castration-resistant prostate cancer.

Research record from J Liq Biopsy, 2026-10-06. PMID 42893057.

Artículo

Analysis of CCR2 gene variants in patients with sarcoidosis using targeted next-generation sequencing: a case-control study.

Research record from Mol Biol Rep, 2026-10-20. PMID 42900239.

Artículo

Flow cytometry-based detection of functional CCR5 variants: A scalable screening approach for HIV-resistant cord blood stem cells.

Research record from Transfusion, 2026-04-08. PMID 41952359.

Artículo

Identification of genetic variants associated with monogenic autoinflammatory diseases in patients with Still's disease using next-generation sequencing.

Research record from Immunol Res, 2026-10-01. PMID 42821198.

Artículo

Multiplex RT-PCR-Based Sequencing Assay to Detect Kidney Cancer-Specific Splice Variants in Tumor Tissues and Plasma Cell-Free RNAs.

Research record from Mol Diagn Ther, 2026-07-06. PMID 42410176.

Artículo

Nanoparticle-enriched mass spectrometry proteomics in British South Asians identifies links between genetic variants, plasma protein levels and disease risk.

Research record from Nat Genet, 2026-07-24. PMID 42498778.

Artículo

Next-Generation Sequencing and Variant Cataloguing for Screening and Diagnosis of Mucolipidoses and Other Lysosome-Related Organelle Disorders, Including Lysosomal Membrane or Transport Disorders.

Research record from Genes (Basel), 2026-05-31. PMID 42353803.

Artículo

Next-generation sequencing-based characterization of BRCA1/2 variants across multiple tumor types in Vietnamese patients.

Research record from BMC Cancer, 2026-07-17. PMID 42464142.

Artículo

Pathogenic Variants and Clinical Outcomes in Korean Dilated Cardiomyopathy Patients: Insights From Next-Generation Sequencing.

Research record from JACC Asia, 2026-03-16. PMID 41837919.

Artículo

Spectrum of actionable genetic variants in acute myeloid leukaemia patients from Pakistan: a study based on next-generation sequencing.

Research record from Ecancermedicalscience, 2026-05-27. PMID 42428814.

Artículo

Systematic reanalysis of next-generation sequencing data in 101 neuromuscular disorder families enhances diagnostic yield, reveals intronic variants, and identifies a novel disease gene.

Research record from J Neurol, 2026-07-20. PMID 42474733.

Anterior 1 2 Siguiente