152 research outputs found
More on heavy tetraquarks in lattice QCD at almost physical pion mass
We report on our progress in studying exotic, heavy tetraquark states,
. Using publicly available dynamical
Wilson-Clover gauge configurations, generated by the PACS-CS collaboration,
with pion masses 164, 299 and 415 MeV, we extend our previous analysis
to heavy quark components containing heavier than physical bottom quarks or , charm and bottom quarks and also only charm quarks
. Throughout we employ NRQCD and relativistic heavy quarks for
the heavier than bottom, bottom and charm quarks. Using our previously
established diquark-antidiquark and meson-meson operator basis we comment in
particular on the dependence of the binding energy on the mass of the heavy
quark component , with heavy quarks ranging from . In the heavy flavor non-degenerate case, ,
and especially for the tetraquark channel , we extend our work
to utilize a GEVP to study the ground and threshold states thereby
enabling a clear identification of possible binding. Finally, we present
initial work on the system where a much
larger operator basis is available in comparison to flavor combinations with
NRQCD quarks.Comment: 8 pages, 5 figures, proceedings contribution to "Lattice 2017. 35th
International Symposium on Lattice Field Theory", 18th-24th June 2017,
Granada, Spai
Evidence for charm-bottom tetraquarks and the mass dependence of heavy-light tetraquark states from lattice QCD
We continue our study of heavy-light four-quark states and find evidence from
lattice QCD for the existence of a strong-interaction-stable
tetraquark with mass in the range of 15 to 61 MeV below
threshold. Since this range includes the electromagnetic
decay threshold, current uncertainties do not allow us to
determine whether such a state would decay electromagnetically, or only weakly.
We also perform a study at fixed pion mass, with NRQCD for the heavy quarks,
simulating and tetraquarks with or
and variable, unphysical in order to investigate the heavy
mass-dependence of such tetraquark states. We find that the dependence of the
binding energy follows a phenomenologically-expected form and that, though
NRQCD breaks down before is reached, the results at higher
clearly identify the channel as the
most likely to support a strong-interaction-stable tetraquark state at
. This observation serves to motivate the direct
simulation. Throughout we use dynamical ensembles
with pion masses 415, 299, and 164 MeV reaching down almost to the
physical point, a relativistic heavy quark prescription for the charm quark,
and NRQCD for the bottom quark(s).Comment: 24 pages, 4 figure
Dark Matter from Strong Dynamics: The Minimal Theory of Dark Baryons
As a simple model for dark matter, we propose a QCD-like theory based on
gauge theory with one flavor of dark quark. The model is confining
at low energy and we use lattice simulations to investigate the properties of
the lowest-lying hadrons. Compared to QCD, the theory has several peculiar
differences: there are no Goldstone bosons or chiral symmetry restoration when
the dark quark becomes massless; the usual global baryon number symmetry is
enlarged to , resembling isospin; and baryons and mesons are
unified together in iso-multiplets. We argue that the lightest
baryon, a vector boson, is a stable dark matter candidate and is a composite
realization of the hidden vector dark matter scenario. The model naturally
includes a lighter state, the analog of the in QCD, for dark
matter to annihilate into to set the relic density via thermal freeze-out. Dark
matter baryons may also be asymmetric, strongly self-interacting, or have their
relic density set via cannibalizing transitions. We discuss some
experimental implications of coupling dark baryons to the Higgs portal.Comment: 26 pages, 16 figure
College student stress: Relationship anxiety, negative affect, self-esteem, and morality-conscience guilt
This poster describes measures of relationship anxiety, negative affect, self-esteem, and morality-conscience guilt used to discuss stress-coping methods of college students
The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing [version 1; referees: 2 approved]
The analytical sensitivity of a next generation sequencing (NGS) test reflects the ability of the test to detect real sequence variation. The evaluation of analytical sensitivity relies on the availability of gold-standard, validated, benchmarking datasets. For NGS analysis the availability of suitable datasets has been limited. Most laboratories undertake small scale evaluations using in-house data, and/or rely on in silico generated datasets to evaluate the performance of NGS variant detection pipelines. Cancer predisposition genes (CPGs), such as BRCA1 and BRCA2, are amongst the most widely tested genes in clinical practice today. Hundreds of providers across the world are now offering CPG testing using NGS methods. Validating and comparing the analytical sensitivity of CPG tests has proved difficult, due to the absence of comprehensive, orthogonally validated, benchmarking datasets of CPG pathogenic variants. To address this we present the ICR639 CPG NGS validation series. This dataset comprises data from 639 individuals. Each individual has sequencing data generated using the TruSight Cancer Panel (TSCP), a targeted NGS assay for the analysis of CPGs, together with orthogonally generated data showing the presence of at least one CPG pathogenic variant per individual. The set consists of 645 pathogenic variants in total. There is strong representation of the most challenging types of variants to detect, with 339 indels, including 16 complex indels and 24 with length greater than five base pairs and 74 exon copy number variations (CNVs) including 23 single exon CNVs. The series includes pathogenic variants in 31 CPGs, including 502 pathogenic variants in BRCA1 or BRCA2, making this an important comprehensive validation dataset for providers of BRCA1 and BRCA2 NGS testing. We have deposited the TSCP FASTQ files of the ICR639 series in the European Genome-phenome Archive (EGA) under accession number EGAD00001004134
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth
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The ICR142 NGS validation series: a resource for orthogonal assessment of NGS analysis [version 2; referees: 2 approved]
To provide a useful community resource for orthogonal assessment of NGS analysis software, we present the ICR142 NGS validation series. The dataset includes high-quality exome sequence data from 142 samples together with Sanger sequence data at 704 sites; 416 sites with variants and 288 sites at which variants were called by an NGS analysis tool, but no variant is present in the corresponding Sanger sequence. The dataset includes 293 indel variants and 247 negative indel sites, and thus the ICR142 validation dataset is of particular utility in evaluating indel calling performance. The FASTQ files and Sanger sequence results can be accessed in the European Genome-phenome Archive under the accession number EGAS00001001332
Structure–function analyses of two plant meso-diaminopimelate decarboxylase isoforms reveal that active-site gating provides stereochemical control
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