Molecular data were generated from terminal restriction fragment length polymorphism (T-RFLP) analysis targeting the 16S rRNA and amoA genes from the sludge community.
At least one molecular evolutionist, Emile Zuckerkandl claimed that molecular data were "'cleaner' material for phyletic investigations than morphological characters" because changes at the molecular level were not likely to be affected by the perturbing influence of the organism's interaction with its environment.
According to the segregation data, molecular data were analyzed using MAPMAKER/EXP 3.0b software (Lander et al. 1987), and linkage map was constructed with MAPDRAW 2.1 (Liu and Meng 2003).
Until recently, trees based on molecular data were derived from analyses of small numbers of genes, the constraint being that DNA sequences were obtained by direct sequencing involving targeted polymerase chain reaction (PCR).
Only molecular data were used for classification of specimens.
Discrepancies between culture and molecular data were numerous and demonstrate that accurate identification remains challenging.
Furthermore, molecular data were used for sub-classification of tissue specimens with regard to Gleason score, age and total serum PSA of the patient at RP.
If the molecular data were still inconsistent with the reported relationship, the individual in question was removed from the analysis (N = 13).
Among 408 patients treated with MAS3 regimen for whom in vivo and molecular data were available, 183 (45%) were infected with parasites with increased pfmdr1 copy number.
Molecular data were imported directly into a FileMaker Pro database (version 10, FileMaker, Inc, Santa Clara, CA) and later merged with survey data in Stata/IC; all statistical analyses were subsequently performed with Stata/IC.
Molecular data were available for seven species.
