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The generation of a national pan-genome, a population-specific catalogue of genetic variation, may advance the impact of clinical genetics studies. Here the Besenbacher et al. carry out deep sequencing and de novo assembly of 10 parent–child trios to generate a Danish pan-genome that provides insight into structural variation, de novomutation rates and variant calling.

Nanoplatelets of molybdenum sulphide have catalytically active sites along their edges that are promising for desulphurizing fuels.

Using sequencing and comparing high-coverage genomes, the germline mutation rates across vertebrates are quantified.

Whole-genome sequencing of 78 Icelandic parent–offspring trios is used to study the de novo mutation rate at the genome-wide level; the rate is shown to increase by about two mutations a year as a function of the increasing age of the father at conception, highlighting the importance of father’s age on the risk of diseases such as autism and schizophrenia.

A renewed interest in C–H bond activation has developed on account of the recent increased availability of shale gas. Now, using a combination of surface science, microscopy, theory and nanoparticle studies, the ability of coke-resistant Pt/Cu single-atom alloys to efficiently activate C–H bonds in alkanes has been demonstrated under realistic catalytic conditions.

Using self-assembly to generate hydrogen-bonded organic networks is an underexplored method when preparing functional framework materials. Now, taking cue from DNA, bio-inspired G-quadruplexes are used as both intrinsic electron donors and hydrogen-bonding linkers to assemble rylene diimide acceptors. The resulting rectangular grids form layered crystalline frameworks, in which photoexcitation produces long-lived mobile charge carriers.

Antihydrogen studies are important in testing the fundamental principles of physics but producing antihydrogen in large amounts is challenging. Here the authors demonstrate an efficient and high-precision method for trapping and stacking antihydrogen by using controlled plasma.

By exploiting the unique structural motifs and self-recognition properties of DNA, it is possible to generate self-assembled DNA nanostructures of specific shapes. Here, a previously described DNA 'origami' method has been extended into three dimensions to create an addressable DNA box on the nanometre scale that can be opened by an externally supplied DNA key'.

Montserrat Garcia-Closas and colleagues report a genome-wide association study for bladder cancer. They identify three new susceptibility loci on chromosomes 22q13.1, 19q12 and 2q37.1.

On-surface synthesis (OSS) defines a special opportunity to investigate intermolecular coupling at. sub-molecular level and has delivered many appealing polymers but so-far OSS is limited to the. lateral covalent bonding of molecular precursors. Here, the authors demonstrate cycloaddition. between C₆₀ and an aromatic compound allowing covalent coupling perpendicular to the surface and multiple non-planar covalent coupling of C₆₀.

Several routes designed to induce a bandgap opening in graphene have been proposed. It is now demonstrated that hydrogen adsorption on the Moiré pattern induced by an iridium substrate can induce a bandgap of 450 meV.

It is not well-understood how nanoscale variations in surface structures impact the ordering of the first few wetting layers on oxide surfaces. Here, the authors employ a model surface, a hydroxylated iron oxide film, which allows direct probing of the impact of hydroxyl groups on the adsorbed water molecules.

The effect of sequence variants on phenotypes may depend on parental origin. Here, a method is developed that takes parental origin — the impact of which, to date, has largely been ignored — into account in genome-wide association studies. For 38,167 Icelanders genotyped, the parental origin of most alleles is determined; furthermore, a number of variants are found that show associations specific to parental origin, including three with type 2 diabetes.

The controllable functionalization of graphene at the molecular level may prove useful for graphene-based electronics, but is difficult to do in a precise fashion. Now it has been shown that a photocycloaddition reaction between a hydrogen-bonded network of maleimide-derived molecules and single-layer graphene can produce a functionalized array with long-range order.

The ALPHA Collaboration reports measurements of the hyperfine components of the 1S–2S transition in trapped antihydrogen. They interpret the results as a test of the invariance of charge–parity–time-reversal symmetry.

Kari Stefansson and colleagues report the whole-genome sequencing of 2,636 individuals from Iceland to a median of 20× coverage, providing a valuable genomic resource for this population isolate. They characterize patterns of genetic variation and population structure and demonstrate the usefulness of this resource for genetic discovery for several disease phenotypes.

A report of high-depth, short-read sequencing and de novo assemblies for 150 individuals from 50 parent–offspring trios as part of establishing a population reference genome for the GenomeDenmark project.

The successful laser cooling of trapped antihydrogen, the antimatter atom formed by an antiproton and a positron (anti-electron), is reported.

Precision measurements of the 1S–2P transition in antihydrogen that take into account the standard Zeeman and hyperfine effects confirm the predictions of quantum electrodynamics.

Paul Pharoah and colleagues report a genome-wide association study for survival time after diagnosis of epithelial ovarian cancer and a parallel analysis of susceptibility to epithelial ovarian cancer. They identified two SNPs at 19p13.11 that associated with susceptibility to the serous subtype of epithelial ovarian cancer.

The hyperfine splitting of antihydrogen has been measured and is consistent with expectations for atomic hydrogen.

Thorunn Rafnar and colleagues identify a variant on 4p16.3 near FGFR3 associated with increased risk of urinary bladder cancer. They find that the risk allele is more frequent among individuals with tumors that carry an activating somatic mutation in FGFR3, suggesting a link between germline variation, somatic mutation status and cancer risk.

The shape of the spectral line and the resonance frequency of the 1S–2S transition in antihydrogen agree very well with those of hydrogen.

The observation of the 1S–2P Lyman-α transition in the antihydrogen atom, the antimatter counterpart of hydrogen, is reported.

The 1S–2S transition in magnetically trapped atoms of antihydrogen is observed, and its frequency is shown to be consistent with that expected for hydrogen.

Simon Gayther and colleagues report a genome wide association study for ovarian cancer. They identify two new susceptibility loci at 2q31 and 8q24 and two suggestive susceptibility loci at 3q25 and 17q21.