Results 81 to 90 of about 90,363 (315)

A Personalized Haplotype‐Resolved Near‐Gapless Genome Framework for Somatic Variant Discovery in Hepatocellular Carcinoma

open access: yesAdvanced Science, EarlyView.
A patient‐specific, haplotype‐resolved genome framework improves detection and interpretation of somatic variants in hepatocellular carcinoma. Using multi‐platform sequencing, the personalized assembly resolves complex regions including centromeres and MHC/HLA loci, enhances structural variant discovery, and links regulatory alterations to allele ...
Jiazheng Lin   +17 more
wiley   +1 more source

Linking DSC/TGA to Cell Levels: Energetics, Evolved Gases, and Thermal Safety of NMC811‐Graphite Micro‐Cell

open access: yesAdvanced Energy Materials, EarlyView.
A bottom‐up, component‐resolved framework combining DSC/TGA, evolved gas analysis, and in situ XRD reveals how decomposition pathways control energy release in partial and micro‐cell configurations. Separator‐free assemblies are dominated by cathode‐O2${\rm O}_2$/anode‐Li reactions, while the separator restricts oxygen transport, reshapes the reaction ...
Ayrton M. Yanyachi   +8 more
wiley   +1 more source

Deepbinner: WGS set basecalled reads [PDF]

open access: yes, 2018
These are the basecalled (FASTQ format) reads for the WGS test set used in the Deepbinner ...
RYAN WICK (1167377)
core   +1 more source

Summary of sequence data of WGS. [PDF]

open access: yes, 2020
Summary of sequence data of WGS.
Yunsu Shi (711297)   +8 more
core   +1 more source

Prenatal Evaluation of RNU4‐2 Variants in Fetuses With Central Nervous System Anomalies

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Fetal central nervous system (CNS) anomalies are among the most common congenital malformations, yet the overall prenatal diagnostic yield of current genetic testing remains below 40%. Variants in RNU4‐2, a non‐coding gene encoding the U4 small nuclear RNA (snRNA), have recently been linked to a novel highly recurrent dominant ...
Yiyao Chen   +13 more
wiley   +1 more source

Deepbinner: WGS set reference genomes [PDF]

open access: yes, 2018
These are the reference genomes (FASTA format) reads for the WGS test set used in the Deepbinner ...
RYAN WICK (1167377)
core   +1 more source

GPS coordinated (WGS) of 50 soil samples [PDF]

open access: yes, 2020
GPS coordinated (WGS) of 50 soil samples
Dama Research Center limited (8358315)
core   +1 more source

Genetic Modifiers of ABCA1 Activity Interact with APOE Isoforms to Mediate Alzheimer's Disease Risk

open access: yesAnnals of Neurology, EarlyView.
Objective ATP‐binding cassette transporter A1 (ABCA1) has been associated with Alzheimer's disease (AD), but the mechanisms by which it impacts disease risk are unknown. ABCA1 is known to bind apolipoprotein E (ApoE) and catalyze apolipoprotein lipidation.
Andrés Peña‐Tauber   +24 more
wiley   +1 more source

Profiling the gut microbiota to assess infection risk in Klebsiella pneumoniae-colonized patients

open access: yesGut Microbes
Vornhagen et al. introduced a model combining gut microbiota structure and Klebsiella pneumoniae genotype to assess infection risk in K. pneumoniae-colonized patients.
Flavio De Maio   +7 more
doaj   +1 more source

Extremely low-coverage whole genome sequencing in South Asians captures population genomics information

open access: yesBMC Genomics, 2017
Background The cost of Whole Genome Sequencing (WGS) has decreased tremendously in recent years due to advances in next-generation sequencing technologies.
Navin Rustagi   +10 more
doaj   +1 more source

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