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Materials Today
Research Hotspot & Journal Scope - next-generation


Materials Today - DOI: 10.1016/J.MATTOD.2018.12.004
Compositionally and structurally redesigned high-energy Ni-rich layered cathode for next-generation lithium batteries

Un Hyuck Kim · Jae Hyung Kim · Jang-Yeon Hwang · Hoon Hee Ryu · Chong Seung Yoon · Yang-Kook Sun ·

Materials Science
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Materials Today - DOI: 10.1016/J.MATTOD.2018.06.008
Graphitic C3N4 quantum dots for next-generation QLED displays

He Liangrui · Mi Fei · Jie Chen · Yunfei Tian · Yang Jiang · Yang Huang · Kai Xu · Juntao Hu · Zhi Zhao · Qiuhong Zhang · Haiyong Ni · Lei Chen ·

Materials Science
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Materials Today - DOI: 10.1016/J.MATTOD.2018.10.034
Aluminum oxide nanowires as safe and effective adjuvants for next-generation vaccines

Rostyslav Bilyy · Solomiya Paryzhak · Kostiantyn Turcheniuk · Tetiana Dumych · Alexandre Barras · Rabah Boukherroub · Fujia Wang · Gleb Yushin · Sabine Szunerits ·

Chemistry
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Next-generation sequencing reads from mouse tissues are mappable to 49% of the human genome and 409 cancer genes.

Impact of mouse contamination in genomic profiling of patient-derived models and best practice for robust analysis [10.1186/s13059-019-1849-2]


This review addresses concepts, approaches, tools, and outcomes of multiscale modeling used to design and optimize the current and next generation rechargeable battery cells.

Boosting Rechargeable Batteries R&D by Multiscale Modeling: Myth or Reality? [10.1021/acs.chemrev.8b00239]


Millimeter-wave (mmWave) bands have shown the potential to enable high data rates for next generation mobile networks.

Robust Beam Tracking and Data Communication in Millimeter Wave Mobile Networks [10.23919/WiOPT47501.2019.9144146]


Here we comprehensively profile murine retinal progenitors by integrating next generation sequencing methods and interrogate changes in chromatin accessibility at embryonic and post-natal stages.

Epigenomic profiling of retinal progenitors reveals LHX2 is required for developmental regulation of open chromatin. [10.1038/s42003-019-0375-9]


MethodsCMV DNA from urine specimens of 30 infants (17 asymptomatic, 13 symptomatic) was target enriched and next generation sequenced resulting in 93% coverage of the CMV genome allowing analysis of viral diversity.

Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection [10.1186/s12879-019-4681-0]


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