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1.
Phys Rev Lett ; 121(2): 021302, 2018 Jul 13.
Article in English | MEDLINE | ID: mdl-30085742

ABSTRACT

We show how a characteristic length scale imprinted in the galaxy two-point correlation function, dubbed the "linear point," can serve as a comoving cosmological standard ruler. In contrast to the baryon acoustic oscillation peak location, this scale is constant in redshift and is unaffected by nonlinear effects to within 0.5 percent precision. We measure the location of the linear point in the galaxy correlation function of the LOWZ and CMASS samples from the Twelfth Data Release (DR12) of the Baryon Oscillation Spectroscopic Survey (BOSS) Collaboration. We combine our linear-point measurement with cosmic-microwave-background constraints from the Planck satellite to estimate the isotropic-volume distance D_{V}(z), without relying on a model-template or "reconstruction" method. We find D_{V}(0.32)=1264±28 Mpc and D_{V}(0.57)=2056±22 Mpc, respectively, consistent with the quoted values from the BOSS Collaboration. This remarkable result suggests that all the distance information contained in the baryon acoustic oscillations can be conveniently compressed into the single length associated with the linear point.

2.
Mon Not R Astron Soc ; 459(3): 3040-3058, 2016 Jul 01.
Article in English | MEDLINE | ID: mdl-27279784

ABSTRACT

We model the luminosity-dependent projected and redshift-space two-point correlation functions (2PCFs) of the Sloan Digital Sky Survey (SDSS) Data Release 7 Main galaxy sample, using the halo occupation distribution (HOD) model and the subhalo abundance matching (SHAM) model and its extension. All the models are built on the same high-resolution N-body simulations. We find that the HOD model generally provides the best performance in reproducing the clustering measurements in both projected and redshift spaces. The SHAM model with the same halo-galaxy relation for central and satellite galaxies (or distinct haloes and subhaloes), when including scatters, has a best-fitting χ2/dof around 2-3. We therefore extend the SHAM model to the subhalo clustering and abundance matching (SCAM) by allowing the central and satellite galaxies to have different galaxy-halo relations. We infer the corresponding halo/subhalo parameters by jointly fitting the galaxy 2PCFs and abundances and consider subhaloes selected based on three properties, the mass Macc at the time of accretion, the maximum circular velocity Vacc at the time of accretion, and the peak maximum circular velocity Vpeak over the history of the subhaloes. The three subhalo models work well for luminous galaxy samples (with luminosity above L*). For low-luminosity samples, the Vacc model stands out in reproducing the data, with the Vpeak model slightly worse, while the Macc model fails to fit the data. We discuss the implications of the modelling results.

3.
Bioinformatics ; 19(14): 1781-6, 2003 Sep 22.
Article in English | MEDLINE | ID: mdl-14512349

ABSTRACT

MOTIVATION: DNA microarray technology and the completion of human and mouse genome sequencing programs are now offering new avenues for the investigation of complex genetic diseases. In particular, this makes possible the study of the spatial distribution of disease-related genes within the genome. We report on the first systematic search for clustering of genes associated with a polygenic autoimmune disease. RESULTS: Using a set of cDNA microarray chip experiments in two mouse models of rheumatoid arthritis, we have identified approximately 200 genes based on their expression in inflamed joints and mapped them into the genome. We compute the spatial autocorrelation function of the selected genes and find that they tend to cluster over scales of a few megabase pairs. We then identify significant gene clusters using a friends-of-friends algorithm. This approach should aid in discovering functionally related gene clusters in the mammalian genome.


Subject(s)
Algorithms , Arthritis, Rheumatoid/genetics , Cluster Analysis , Gene Expression Regulation/genetics , Genetic Testing/methods , Oligonucleotide Array Sequence Analysis/methods , Sequence Alignment/methods , Sequence Analysis, DNA/methods , Animals , Base Sequence , Gene Expression Profiling/methods , Genetic Predisposition to Disease/genetics , Mice , Molecular Sequence Data , Pattern Recognition, Automated
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