<u>Answer:</u>
<em>A constant is something whose value cannot be changed and is used for comparison purpose. </em>
<u>Explanation:</u>
The controlled variable is a type of variable whose value is kept constant during the experiment to get the desired or expected result. The difference between constant and a control variable is that the constant can never be changed.
However, the value of control variable can be changed but is kept constant with a purpose in an experiment to get the data. The controlled variable in a battery can be the multi meter that should be used for all the batteries.
<span>The branch of
anatomy that focuses on body structures that are visible to the naked eye is
called gross anatomy. It is only concern with macroscopic details and therefore
do not need any aid of instrument. Gross anatomy is used to study dead bodies
that uses two approaches. The systemic approach, studied the different system
of the body while in regional approach, human body is studied in different regions. </span>
<span> </span>
The answer is D. The first two arent pollinated by bees,
The most grown crop in the US is corn, followed by soybeans and wheat.
Answer:
1. Map-based genome sequencing: a; c; f; g
2. Whole-genome shotgun sequencing: b
3. Both sequencing methods: d; e
Explanation:
Map-based genome sequencing is a method that makes use of a reference genome sequence in order to determine the relative position of the DNA fragments before they are sequenced. This method is useful to determine the position of repetitive DNA fragments (for example, duplicated genes, repetitive non-coding regions, etc.) and Transposable Elements. Therefore, map-based genome sequencing is a suitable approach for large genomes (which are usually composed of repetitive sequences). On the other hand, in whole-genome shotgun sequencing, DNA sequences are obtained before the correct order of these DNA fragments is known. In this method, the genome is fragmented randomly into small DNA sequences (between 100 and 1000 base pairs), which are subsequently sequenced through the chain-termination sequencing approach (i.e., Sanger sequencing) and finally ordered by using bioinformatic tools that assemble overlapping reads.
