2018
DOI: 10.1007/s12041-018-1017-6
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Noninvasive DNA-based species and sex identification of Asiatic wild dog ( $${\varvec{Cuon~alpinus}}$$ C u o n a l p i n u

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Cited by 12 publications
(11 citation statements)
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“…We got a male biased sex-ratio (4:1) in this pilot study. While there is no conclusive information on dhole sex ratio across its range, our earlier study (Modi et al, 2018) in the same landscape has shown a male biased (M:F ratio of 3:1) sex ratio, and ecological study in southern India by Venkataraman (1998) suggested male biased packs. Future studies with extensive genetic sampling across this landscape would potentially provide more accurate sex ratio for dholes.…”
Section: Discussionmentioning
confidence: 57%
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“…We got a male biased sex-ratio (4:1) in this pilot study. While there is no conclusive information on dhole sex ratio across its range, our earlier study (Modi et al, 2018) in the same landscape has shown a male biased (M:F ratio of 3:1) sex ratio, and ecological study in southern India by Venkataraman (1998) suggested male biased packs. Future studies with extensive genetic sampling across this landscape would potentially provide more accurate sex ratio for dholes.…”
Section: Discussionmentioning
confidence: 57%
“…Once the initial temperature and multiplexing standardisations were performed using reference blood DNA samples, final standardisation was conducted with dhole faecal DNA. Species identification was performed for all field-collected faeces using specific mtDNA primers described in Modi et al (2018). PCR reactions were performed with four μl of hotstart taq mix (QIAGEN Inc., Hilden, Germany), four μM BSA, 0.5 μM of primer mix and three μl of DNA extract with conditions including initial denaturation (95 °C for 15 min); 50 cycles of denaturation (94 °C for 30 s), annealing (50 °C for 30 s) and extension (72 °C for 35 s); followed by a final extension (72 °C for 10 min).…”
Section: Methodsmentioning
confidence: 99%
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“…A total of 623 samples were collected from six protected areas during the study period (2016–2019). We identified 590 dhole faeces through species-specific molecular assay 27 , attaining an amplification success of 94%. Using a panel of 12 microsatellite markers 26 , we generated a dataset of 349 genotypes attaining a success rate of 59.1%.…”
Section: Resultsmentioning
confidence: 99%
“…Fecal molecular biotechnology provides a rapid and dependable way of sampling endangered animals [1114]. In addition, with the development of molecular biology technology, fecal DNA is extensively used in genetic biology studies for species identification [1517], individual identification [1820], sex identification [2125], population genetic structure [2628], and genetic diversity evaluation [29]. However, fecal sampling has some problems, such as poor fecal DNA isolation quality and low success rate of PCR amplification [30].…”
Section: Introductionmentioning
confidence: 99%