Results 51 to 60 of about 864,768 (299)

Microstructure from ferroelastic transitions using strain pseudospin clock models in two and three dimensions: a local mean-field analysis [PDF]

open access: yes, 2010
We show how microstructure can arise in first-order ferroelastic structural transitions, in two and three spatial dimensions, through a local meanfield approximation of their pseudospin hamiltonians, that include anisotropic elastic interactions.
A. G. Khachaturyan   +9 more
core   +2 more sources

Shiny-SoSV: A web-based performance calculator for somatic structural variant detection.

open access: yesPLoS ONE, 2020
Somatic structural variants are an important contributor to cancer development and evolution. Accurate detection of these complex variants from whole genome sequencing data is influenced by a multitude of parameters. However, there are currently no tools
Tingting Gong   +2 more
doaj   +1 more source

A Labelled Sequent Calculus for BBI: Proof Theory and Proof Search

open access: yes, 2015
We present a labelled sequent calculus for Boolean BI, a classical variant of O'Hearn and Pym's logic of Bunched Implication. The calculus is simple, sound, complete, and enjoys cut-elimination.
Gore, Rajeev, Hou, Zhe, Tiu, Alwen
core   +1 more source

Clinical Insights Into Hypercalcemia of Malignancy in Childhood

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Hypercalcemia of malignancy (HCM) is a rare but life‐threatening metabolic emergency in children that occurs in less than 1% of pediatric cancer cases, with a reported incidence ranging from 0.4% to 1.0% across different studies. While it is observed in 10%–20% of adult malignancies, pediatric HCM remains relatively uncommon.
Hüseyin Anıl Korkmaz
wiley   +1 more source

Whole-genome sequencing of phenotypically distinct inflammatory breast cancers reveals similar genomic alterations to non-inflammatory breast cancers

open access: yesGenome Medicine, 2021
Background Inflammatory breast cancer (IBC) has a highly invasive and metastatic phenotype. However, little is known about its genetic drivers. To address this, we report the largest cohort of whole-genome sequencing (WGS) of IBC cases.
Xiaotong Li   +15 more
doaj   +1 more source

Inpatient Food Insecurity and Pediatric Hematology Oncology Hospitalization Outcomes

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Children with cancer and blood disorders are at risk for food insecurity (FI). We aimed to describe the association of inpatient food insecurity (IFI) and hospitalization outcomes among patients admitted to the pediatric hematology oncology service. Of 325 caregivers screened for IFI, 60 (18.6%) screened positive.
Joanna M. Robles   +4 more
wiley   +1 more source

Chromoanagenesis in Osteosarcoma

open access: yesBiomolecules
Chromoanagenesis is a catastrophic genomic phenomenon involving sudden, extensive rearrangements within one or a few cell cycles. In osteosarcoma, the most prevalent malignant bone tumor in children and adolescents, these events dramatically alter the ...
Guozhuang Li   +9 more
doaj   +1 more source

Effect of aluminium sheet surface conditions on feasibility and quality of resistance spot welding [PDF]

open access: yes, 2010
A study investigating the effect of sheet surface condition on resistance spot welding (RSW) of aluminium has been carried out. This concentrates on two automotive aluminium alloys; AA5754 and AA6111, used for structural and closure applications ...
Briskham   +14 more
core   +1 more source

Prioritisation of structural variant calls in cancer genomes [PDF]

open access: yesPeerJ, 2017
Sensitivity of short read DNA-sequencing for gene fusion detection is improving, but is hampered by the significant amount of noise composed of uninteresting or false positive hits in the data.
Miika J. Ahdesmäki   +14 more
doaj   +2 more sources

Nanopore sequencing in human genetic studies: application to structural variant detection [PDF]

open access: yes, 2019
Background: Nanopore sequencing is a recent technology which allows direct real-time sequencing of DNA or RNA molecules and production of read lengths as long as the size of the original fragments.
Silva, Catarina, Vieira, Luís
core  

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