Next-Generation Sequencing of a Family With a High Penetrance of Monoclonal Gammopathies for the Identification of Candidate Risk Alleles

Cancer - United States
doi 10.1002/cncr.30777
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Optimized Selection of Unrelated Subjects for Whole-Genome Sequencing Studies of Rare High-Penetrance Alleles

Genetic Epidemiology
EpidemiologyGenetics
2012English

DNA-based Diagnosis of Uncharacterized Inherited Macrothrombocytopenias Using Next-Generation Sequencing Technology With a Candidate Gene Array

2016English

Imputation of TPMT Defective Alleles for the Identification of Patients With High-Risk Phenotypes

Frontiers in Genetics
GeneticsMolecular Medicine
2014English

Preimplantation High Resolution HLA Sequencing Using Next Generation Sequencing

Biology of Blood and Marrow Transplantation
TransplantationHematology
2018English

Identification of Hepatotropic Viruses From Plasma Using Deep Sequencing: A Next Generation Diagnostic Tool

PLoS ONE
Multidisciplinary
2013English

Next Generation Sequencing

Methods in Molecular Biology
GeneticsMolecular Biology
2018English

Next-Generation Sequencing Coupled With a Cell-Free Display Technology for High-Throughput Production of Reliable Interactome Data

Scientific Reports
Multidisciplinary
2012English

Targeted Next-Generation Sequencing Identified a Novel ANK1 Mutation Associated With Hereditary Spherocytosis in a Chinese Family

Hematology
Hematology
2019English

Next-Generation Sequencing

2016English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy