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wandering17

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2015
Is There a Genetic Marker for Dyslexia?

A disruption of a gene called DYXC1 on chromosome 15 for humans may be related to an increased risk of developing dyslexia. Researchers1 studied the gene in 109 people diagnosed with dyslexia and in a control group of 195 others who had no learning disorder. The DYXC1 break occurred in 10 of those with dyslexia and in 5 of those in the control group.

(b) How many rows and how many columns will the data table have? Assume rows are the cases and columns are the variables. (There might be an extra column for identification purposes; do not count this column in your total.)
 

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