Nanopore Sequencing in Blood Diseases: A Wide Range of Opportunities-Reference-Cited by-同舟云学术

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Nanopore Sequencing in Blood Diseases: A Wide Range of Opportunities

Published:2020-02-19 Issue: Volume:11 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Minervini Crescenzio Francesco,Cumbo Cosimo,Orsini Paola,Anelli Luisa,Zagaria Antonella,Specchia Giorgina,Albano Francesco

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference82 articles.

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2. WHO Klassifikation 2016;Amriah;Blood,2006

3. Rapid detection of chromosomal translocation and precise breakpoint characterization in acute myeloid leukemia by nanopore long-read sequencing;Au;Cancer Genet.,2019

4. Promoter-bound METTL3 maintains myeloid leukaemia via m6A-dependent translation control Europe PMC Funders Group;Barbieri;Nature,2017

5. Profiling DNA Methylation based on next-generation sequencing approaches: new insights and clinical applications;Barros-Silva;Genes,2018

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1. Comparative Analyses of Targeted Myeloid Cancer Next-Generation Sequencing Panel in Fresh Blood, Bone Marrow and FFPE Material;International Journal of Molecular Sciences;2024-03-21

2. The whole is greater than the sum of its parts: Long‐read sequencing for solving clinical problems in haematology;Journal of Cellular and Molecular Medicine;2024-01-23

3. The potential of 3rd‐generation nanopore sequencing for B‐cell clonotyping in lymphoproliferative disorders;eJHaem;2023-11-23

4. Case report: biallelic DNMT3A mutations in acute myeloid leukemia;Frontiers in Oncology;2023-06-28

5. Nanopore single-molecule analysis of biomarkers: Providing possible clues to disease diagnosis;TrAC Trends in Analytical Chemistry;2023-05

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