scholarly journals Editorial for Brain Sciences Special Issue: “Diagnosis of Neurogenetic Disorders: Contribution of Next-Generation Sequencing and Deep Phenotyping”

2019 ◽  
Vol 9 (3) ◽  
pp. 72
Author(s):  
Alisdair McNeill

In this Special Issue we bring together papers demonstrating the need for both detailed genomic and phenotypic studies to aid our scientific and clinical understanding of neurogenetic disorders [...]

Genes ◽  
2018 ◽  
Vol 9 (10) ◽  
pp. 505
Author(s):  
Manfred Grabherr ◽  
Bozena Kaminska ◽  
Jan Komorowski

The massive increase in computational power over the recent years and wider applicationsof machine learning methods, coincidental or not, were paralleled by remarkable advances inhigh-throughput DNA sequencing technologies.[...]


2016 ◽  
Vol 136 (9) ◽  
pp. S191
Author(s):  
S. Polubothu ◽  
R. Knox ◽  
L. Al-Olabi ◽  
V. Parker ◽  
R. Semple ◽  
...  

Viruses ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 340
Author(s):  
Rami Kantor

Drug resistance remains a global challenge in the fight against the HIV pandemic [...]


2008 ◽  
Vol 86 (2) ◽  
pp. 81-91 ◽  
Author(s):  
Olena Morozova ◽  
Marco A. Marra

Genome rearrangements have long been recognized as hallmarks of human tumors and have been used to diagnose cancer. Techniques used to detect genome rearrangements have evolved from microscopic examinations of chromosomes to the more recent microarray-based approaches. The availability of next-generation sequencing technologies may provide a means for scrutinizing entire cancer genomes and transcriptomes at unparalleled resolution. Here we review the methods that have been used to detect genome rearrangements and discuss the scope and limitations of each approach. We end with a discussion of the potential that next-generation sequencing technologies may offer to the field.


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