1.Conduct responsible research to escape from predatory journals
Annals of Dentistry 2021;28(1):32-33
		                        		
		                        			
		                        			Academics and researchers, willingly or unwillingly, continue to fall a “victim” to predatory journals. The entire 
cascade of moving forward in academia depends on one’s ability to publish papers - as many as possible and 
in the shortest possible time. Such a requirement for a “number” persuades an academician or a researcher to 
race for an increased number of papers rather than to ensure the quality of the papers they want to publish. 
Thanks, but no thanks to the predatory journals - for providing a comfortable avenue for those papers to get 
published. An effective way out could be to train the academics and create awareness among them to conduct 
research following the codes of responsible research. Policymakers may also need to consider adopting policies 
that will not force their academic and research staff to race against time and compromise the codes of 
responsible research.
		                        		
		                        		
		                        		
		                        	
2. Novel PCR primers to diagnose visceral leishmaniasis using peripheral blood, spleen or bone marrow aspirates
Mahbuba KHATUN ; S.M. Sabbir ALAM ; M. Anwar HOSSAIN ; Muhammad Manjurul KARIM ; Abed Hussain KHAN ; Jalaluddin Ashraful HAQ ; Md. Shariful ALAM JILANI ; Mohammad Tariqur RAHMAN
Asian Pacific Journal of Tropical Medicine 2017;10(8):753-759
		                        		
		                        			
		                        			 Objective To establish a suitable method of diagnosis of visceral leishmaniasis (VL) using peripheral blood, spleen or bone marrow aspirates. Methods Peripheral blood, bone marrow and spleen aspirate samples were collected from clinically suspected VL patients (n = 26). A new PCR primer pair (MK1F/R) was designed targeting kinetoplast mini circle DNA sequences of Leishmania donovani, and Leishmania infantum, and was used to diagnose VL along with some other established primers for VL in polymerase chain reactions. Test was validated by comparing with several other diagnostic methods. Results The designed primer set showed 100% specificity and 98% sensitivity in detecting VL using blood samples, when compared with more invasive samples: bone marrow or spleen aspirates. Conclusions The newly designed primer MK1F/R could be a better alternative for PCR based diagnosis of VL using less invasive sample, peripheral blood instead of bone marrow or spleen aspirates. 
		                        		
		                        		
		                        		
		                        	
            

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