A Parton Model for Inclusive Semileptonic B Meson Decays

The parton model for semileptonic B meson decays is studied with special attention to the decay distributions. We find that the spectra show dramatic variations when we introduce cuts on the hadronic energy or invariant mass of hadrons. Results for both $b\rightarrow u$ and $b\rightarrow c$ decays are presented. The detailed spectra may help to separate the two types of decays.Comment: 9 pages, DO-TH 93/29, OHSTPY-HEP-T-93-011, September 199

Probing for the Charm Content of BB and Υ\Upsilon Mesons

A slow $J/\psi$ bump exists in the inclusive $B\to J/\psi + X$ spectrum, while the softness of $J/\psi$ spectrum in $\Upsilon(1S) \to J/\psi + X$ decay is in strong contrast with expectations from color octet mechanism. We propose {\it intrinsic} charm as the explanation:the former is due to $\bar B\to J/\psi D \pi$,with three charm quarks in the final state; the latter is just a small fraction of $\Upsilon(1S) \to (c\bar c)_{\rm slow} + 2$"jet" events, where the slow moving $c\bar c$ system evolves into $D^{(*)}$ pairs. Experimental search for these phenomena at B Factories and the Tevatron is strongly urged, as the implications go beyond QCD.Comment: 4 pages, REVTEX, 10 eps figures included. Major revision with more discussions on the rescattering background, and a reappraisal of the Upsilon(1S) decay in the presence of intrinsic charm, leading to a change in Titl

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

A major use of the 1000 Genomes Project (1000GP) data is genotype imputation in genome-wide association studies (GWAS). Here we develop a method to estimate haplotypes from low-coverage sequencing data that can take advantage of single-nucleotide polymorphism (SNP) microarray genotypes on the same samples. First the SNP array data are phased to build a backbone (or 'scaffold') of haplotypes across each chromosome. We then phase the sequence data 'onto' this haplotype scaffold. This approach can take advantage of relatedness between sequenced and non-sequenced samples to improve accuracy. We use this method to create a new 1000GP haplotype reference set for use by the human genetic community. Using a set of validation genotypes at SNP and bi-allelic indels we show that these haplotypes have lower genotype discordance and improved imputation performance into downstream GWAS samples, especially at low-frequency variants. © 2014 Macmillan Publishers Limited. All rights reserved