1999
DOI: 10.1007/s004360050645
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Analysis of helminth genetic data: comparative examples with Haemonchus contortus isozymes using exact tests or resampling procedures

Abstract: Population genetic data on helminths are scarce and it is important to fine tune analyses of these data, the interpretation of which is based on between-(Fst) and within-(Fis) population variability. Several computer programs are available and confidence intervals of each index are based on different procedures. These programs (Genetix, Diploid, Genepop) were compared with a classical program (Biosys-1) using a large set of Haemonchus contortus isozyme data. The results were identical for all softwares for lar… Show more

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Cited by 11 publications
(5 citation statements)
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“…STR repeat frequencies can be obtained from the corresponding author on request. Thereafter, the CLUMP, 49 CHECKHET, 50 GENEPOP, 51 POWERMARKER 52 and STRUCTURE 53 software packages were used to investigate for population stratification both between as well as within the patient and the control sample.…”
Section: Genomic Controlmentioning
confidence: 99%
“…STR repeat frequencies can be obtained from the corresponding author on request. Thereafter, the CLUMP, 49 CHECKHET, 50 GENEPOP, 51 POWERMARKER 52 and STRUCTURE 53 software packages were used to investigate for population stratification both between as well as within the patient and the control sample.…”
Section: Genomic Controlmentioning
confidence: 99%
“…In particular, studies on wild animals (Bentousi & Cabaret, 1999; Braisher et al , 2004) identified different host specificity, local adaptation or other factors, which in turn could influence nematode spreading, interspecific transmission and management. The study of parasite population genetics (Criscione et al , 2005; Troell et al , 2006) has recently been supported by the development of a variety of molecular marker analyses.…”
Section: Introductionmentioning
confidence: 99%
“…Over the years, numerous 'first-generation' molecular and biochemical methods have been developed for identifying Haemonchus species and for examining drug-resistant genotypes. Restriction enzyme digestion followed by agarose gel electrophoresis (Beh et al, 1989), Southern blotting (Roos et al, 1990;Zarlenga et al, 1994), repetitive DNA hybridization probes in conjunction with Southern blots or dot blots (Christensen et al, 1994a,b), and isoenzyme banding profiles (Bentounsi and Cabaret, 1999;Echevarria et al, 1992;Knox and Jones, 1992) were among the most popular examples of first-generation technologies. Sensitivity and specificity, however, were key issues that prompted the transition to PCR-based assays for developing more advanced tests.…”
Section: Molecular Methods For Identifying Haemonchus 31 Haemonchus mentioning
confidence: 99%