17 research outputs found
A Comparison of two different jet algorithms for the top mass reconstruction at the LHC
We compare the abilities of the cluster-type jet algorithm, KtJet, and a
mid-point iterating cone algorithm to reconstruct the top mass at the LHC. We
discuss the information contained in the merging scales of cluster-type
algorithms, and how this can be used in experimental analyses, as well as the
different sources of systematic errors for the two algorithms. We find that the
sources of systematic error are different for the two algorithms, which may
help to better constrain the systematic error on the top mass at the LHC.Comment: 21 pages, 16 figures, accepted by JHE
TeVJet: A general framework for the calculation of jet observables in NLO QCD
In this paper we present the parton level Monte Carlo program TeVJet, a
direct implementation of the dipole subtraction method for calculating jet
cross sections in NLO QCD. It has been written so as to allow the inclusion of
new processes in as straightforward a way as possible. The user must provide
the usual ingredients for an NLO calculation and from these the
process-independent parts required to make the phase space integrals finite in
4 dimensions are automatically generated. These integrals are then performed
using Monte Carlo techniques. We present the results for a few example
processes.Comment: 52 pages, program available from
http://www.hep.man.ac.uk/u/chris/tevje
Top quark phenomenology at the large hadron collider
EThOS - Electronic Theses Online ServiceGBUnited Kingdo
Single-Cell RNA Sequencing Reveals Fibroblast Heterogeneity Across Mouse and Human Embryonic Origins
Identification and characterization of an injury-induced skeletal progenitor
Photograph of a roundup scene at the Joseph H. Williams Tallgrass Prairie Preserve
Assessment of Viability of Human Fat Injection into Nude Mice with Micro-Computed Tomography
Isolation and Enrichment of Human Adipose-derived Stromal Cells for Enhanced Osteogenesis
Bone marrow-derived mesenchymal stromal cells (BM-MSCs) are considered the gold standard for stem cell-based tissue engineering applications. However, the process by which they must be harvested can be associated with significant donor site morbidity. In contrast, adipose-derived stromal cells (ASCs) are more readily abundant and more easily harvested, making them an appealing alternative to BM-MSCs. Like BM-MSCs, ASCs can differentiate into osteogenic lineage cells and can be used in tissue engineering applications, such as seeding onto scaffolds for use in craniofacial skeletal defects. ASCs are obtained from the stromal vascular fraction (SVF) of digested adipose tissue, which is a heterogeneous mixture of ASCs, vascular endothelial and mural cells, smooth muscle cells, pericytes, fibroblasts, and circulating cells. Flow cytometric analysis has shown that the surface marker profile for ASCs is similar to that for BM-MSCs. Despite several published reports establishing markers for the ASC phenotype, there is still a lack of consensus over profiles identifying osteoprogenitor cells in this heterogeneous population. This protocol describes how to isolate and use a subpopulation of ASCs with enhanced osteogenic capacity to repair critical-sized calvarial defects
