Cells enriched from patients with AML could be divided into populations that differed in the expression of specific surface molecules.
Our data are therefore consistent with the previously suggested hypothesis that MaSp1 locus variants could be incorporated in differing proportions into draglines [ 35].
Furthermore, patients classified as low risk based on the 'cell death' signature, but not those classified as high risk on this basis, could be separated into groups of differing outcome on the basis of the 'cell cycle' signature (p = 0.015 and 0.67, respectively; Fig. 7D).
Tumors could be classified into five clusters that differed by their AG percentages and aberration patterns.
Hybrids in the diversity panel could be grouped into eight breeding populations differing in mean performance.
Many of the neurons were reported to be non-spiking [ 41], and AMMC-B1 neurons, for example, could be classified into four subtypes that differ in their sensitivities and frequency characteristics [ 42 ].
Thus, while the tools are currently coded to work for the SNP or PCR-RFLP analyses described here, any type of marker such as microarray hybridization patterns, microsatellite markers, or even chemical or physical features that differ among isolates could be categorized into haplotypes and fed into the back end of the combinatorial analyses described below.
Each of these could be expressed by differing rhythms and harmonies.
The significant network modules identified through this approach differed between the six HLA risk groups, which could be divided into two groups based on carrying the DRB1*0301 or the DRB1*0401 allele.
Analysis of the 158 reads showed that all but 31 of them could be grouped into one of 42 groups, the members of which differed by no more than five percent, which could have been due to allelic variation.
