I would like a discussion section based on the mutations I have identified in the Bangladeshi patients whose DNA I have sequenced and their family members. I have all the results at hand (sequencing traces and PCR pictures) and have drawn the family trees. I require help interpreting these and commenting on their segregation patterns, modes of inheritance, odds ratios and any other relevant interpretations with a critique. The sequencing traces are in the word document and the pedigrees which need to be included in the discussion section are in the powerpoint so they simply need to be transferred into the word document of the discussion you will write. I also have an excel spreadsheet with other details about those patients i.e. if they also have asthma, hay fever, which would be useful to tabulate. So column 1: patient number, column 2: eczema (Y/N), column 3: asthma (Y/N), column 4: allergic rhinitis (hay fever) (Y/N). And then any interpretations about these correlations & findings. I.e. do those patients with eczema also have the other conditions. Why? Etc. Further work that can be done to improve power, reliability, accuracy of the study. Diagrams and figures must be labelled. Many thanks & please contact me at any time. I have attached the results in word, the pedigrees relating to these in powerpoint and the Excel spreadsheet.
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