Description of superdeformed bands in light N=Z nuclei using the cranked HFB method

Superdeformed states in light $N=Z$ nuclei are studied by means of the self-consistent cranking calculation (i.e., the P + QQ model based on the cranked Hartree-Fock-Bogoliubov method). Analyses are given for two typical cases of superdeformed bands in the $A \simeq 40$ mass region, that is, bands where backbending is absent ($^{40}$Ca) and present ($^{36}$Ar). Investigations are carried out, particularly for the following points: cross-shell excitations in the sd and pf shells; the role of the g$_{9/2}$ and d$_{5/2}$ orbitals; the effect of the nuclear pairing; and the interplay between triaxiality and band termination.Comment: 17 pages, 18 figures, accepted in Phys. Rev.

Comparison of TCGA and GENIE genomic datasets for the detection of clinically actionable alterations in breast cancer.

Whole exome sequencing (WES), targeted gene panel sequencing and single nucleotide polymorphism (SNP) arrays are increasingly used for the identification of actionable alterations that are critical to cancer care. Here, we compared The Cancer Genome Atlas (TCGA) and the Genomics Evidence Neoplasia Information Exchange (GENIE) breast cancer genomic datasets (array and next generation sequencing (NGS) data) in detecting genomic alterations in clinically relevant genes. We performed an in silico analysis to determine the concordance in the frequencies of actionable mutations and copy number alterations/aberrations (CNAs) in the two most common breast cancer histologies, invasive lobular and invasive ductal carcinoma. We found that targeted sequencing identified a larger number of mutational hotspots and clinically significant amplifications that would have been missed by WES and SNP arrays in many actionable genes such as PIK3CA, EGFR, AKT3, FGFR1, ERBB2, ERBB3 and ESR1. The striking differences between the number of mutational hotspots and CNAs generated from these platforms highlight a number of factors that should be considered in the interpretation of array and NGS-based genomic data for precision medicine. Targeted panel sequencing was preferable to WES to define the full spectrum of somatic mutations present in a tumor

The isovector dipole strength in nuclei with extreme neutron excess

The E1 strength is systematically analyzed in very neutron-rich Sn nuclei, beyond $^{132}$Sn until $^{166}$Sn, within the Relativistic Quasiparticle Random Phase Approximation. The great neutron excess favors the appearance of a deformed ground state for $^{142-162}$Sn. The evolution of the low-lying strength in deformed nuclei is determined by the interplay of two factors, isospin asymmetry and deformation: while greater neutron excess increases the total low-lying strength, deformation hinders and spreads it. Very neutron rich deformed nuclei may not be as good candidates as stable spherical nuclei like $^{132}$Sn for the experimental study of low-lying E1 strength

The association between life events, social support, and antibody status following thymus-dependent and thymus-independent vaccinations in healthy young adults

This study determined whether stressful life events and social support were related to antibody status following both thymus-dependent and thymus-independent vaccinations. Life events in the previous year and customary social support were measured in 57 healthy students at baseline. Antibody status was also assessed at baseline and at five weeks and five months following vaccination with the trivalent influenza vaccine and the meningococcal A+C polysaccharide vaccine. Taking into account baseline antibody titre, high life events scores prior to vaccination were associated with lower responses to the B/Shangdong influenza strain at both five weeks and five months and meningococcal C at five weeks. Life events scores were not associated with response to the other two influenza viral strains nor response to meningococcal A. Those with high social support scores had stronger 5-week and 5-month antibody responses to the A/Panama influenza strain, but not to any of the other strains. These associations could not be accounted for by demographic or health behaviour factors, and also emerged from analyses comparing those who exhibited a four-fold increase in antibody titre from baseline with those who did not. Life events and social support were related to antibody status following influenza vaccination in distinctive ways that may be partly determined by vaccine novelty and prior naturalistic exposure. Life events also predicted poor antibody response to meningococcal C polysaccharide vaccination after previous meningococcal C conjugate vaccination. Neither psychosocial factor was associated with response to primary meningococcal A polysaccharide vaccination