Canthium wenzelii and Canthium sp. What will happen to the two Canthium species, which have their own synapomorphies distinct from the Keetia group?
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Canthium wenzelii and Canthium sp. What will happen to the two Canthium species, which have their own synapomorphies distinct from the Keetia group?
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- With the information that a Wright- Fisher population have a size of 10,000 and assume that mutation rate is 2.5x10-8 per site per generation. What is the probability of difference between the two sequences that were randomly taken from the population? Show all working and explanation.(a) Explain sensitivity and selectivity in terms of true and false positives. (b) What is the advantage of a Needleman-Wunsch alignment compared to a seeded alignment? (c) What does the expectation parameter mean in local alignment? What will happen if the expectation value is increased from its default value of 10 to a 100?What is the 1% extinction value of the protein used to calibrate this experiment? I obtained a gradient of 0.0021, into which units should this be presented?
- What was studied or investigated in the paper? Who would be affected by this? https://opus.lib.uts.edu.au/bitstream/10453/31887/1/2012007630OK.pdfa - What is Position-Specific Scoring Matrices (PSSM) and how do we obtain it? b - Construct the HMM for the following sequences where the matches are considered for the columns that don't have any gap T G A C А G T G A А G G T G G A G G C A G EE E E EPlease consider Figure 8.8 (attached below) in the textbook (Figure 8.7 in the 4TH edition), which contains data that were obtained by Clegg et al., is redepicted from their paper that was published in 1980, and for which information is provided on pp. 300-302 in the textbook (pp. 289-291 in the 4TH edition textbook); assess comprehensively the lowercase-Roman-numeral-labelled statements that appear immediately below; and click the uppercase-letter-labelled response that is presented below and conveys the most accurate information. i. At generation 0, the populations were characterised by D = -1 or D = 1.ii. The D value changes could have resulted from processes including crossing over during meiosis.iii. The D values changed by the factor (1- r) each generation.iv. At generation 0, the populations were characterised by D = -0.25 or D = 0.25.v. At generation 0, the populations were characterised by extreme values, representing complete linkage disequilibrium. Question 1 options:…
- Explain the multiple testing problem of GWAS - why do we need such a small p-value to achieve significance?Hi, I would like to know which program is used for the graphical presentation of the results of a meta-analysis of genome-wide linkage scans?Why a multiple sequence alignment is needed for researchers? What inferences can be derived from this kind of sequence alignments? Explain two extreme cases that are non-informative for the multiple sequence alignment.
- The following table are the results of spectrophotomety of extracted RNA samples (note: not all OD's reported in this table are relevant for all subsequent questions). Specrophotometry- RNA Extractions Experimental Group Replicate O0260 OD280 OD320 00360 1 0.68 0.38 0.70 0.73 2 1.35 0.75 146 1.38 1.85 1.03 1.93 1.96 1 0.68 0.38 0.80 0.85 2 180 1.00 1.96 1.98 0.96 0.53 1.11 1.18 What is the SSRNA concentration for sample A1? Select one: O a 273 ug/ml O b. 18.9 ug/ml Oc 34.1 ug/ml O d 15.1 ug/ml O e 22.5 ug/mlIn a typical PCR reaction what is happening in stages occurring at temperature ranges (a) 92–95°C, (b) 45–65°C, and (c) 65–75°C.What type of research is this? Explain.What do the results indicate? Their implications?https://opus.lib.uts.edu.au/bitstream/10453/31887/1/2012007630OK.pdf