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use the data shared in the following galaxy history: https://usegalaxy.org/u/jpdemuth/h/parent1. The history contains a Paired-End Dataset Collection from one parent that was included in the 1000 Genomes project parent-offspring trios. Use Human genome assembly build 38 (hg38) as the reference genome for your analysis. Copy/Paste the bar chart showing results of "Number of effects by type and region" from the SnpEff output. Based on the Number of effects by type and region chart: Which two types of regions have the most variants? The pattern observed in the chart is typical for any human we could have analyzed. Does this pattern suggest that most polymorphic sites in humans are adaptive, neutral, or deleterious? Justify why you chose adaptive, neutral or deleterious in the previous question..

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use the data shared in the following galaxy history: https://usegalaxy.org/u/jpdemuth/h/parent1. The history contains a Paired-End Dataset Collection from one parent that was included in the 1000 Genomes project parent-offspring trios. Use Human genome assembly build 38 (hg38) as the reference genome for your analysis. Copy/Paste the bar chart showing results of "Number of effects by type and region" from the SnpEff output. Based on the Number of effects by type and region chart: Which two types of regions have the most variants? The pattern observed in the chart is typical for any human we could have analyzed. Does this pattern suggest that most polymorphic sites in humans are adaptive, neutral, or deleterious? Justify why you chose adaptive, neutral or deleterious in the previous question.

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