Different structure in an organism are specialized to perform different tasks in the organism depending on their makeup. A few examples are:
Heart, veins, arteries are structures forming the cardiovascular system and function is to facilitate transport nutrients and oxygen carried by blood all over the body.
Bones, joints, ligaments and cartilage are structures of the skeletal system and their function is support and protection of the body.
Mouth, esophagus. stomach, large and small intestines are structures of the digestive system and their function is to break down food and absorb nutrients.
The answer would be : <span>B. the Casparian strip is waterproof.
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Photon</span>
True
A genotype is the combination of genes in its DNA of the organism that determines its traits
Explanation:
Gametes from parents contribute different alleles of genes to their offspring. This why gametes carry only one copy of genetic material of the organism. They later fuse to form a zygote with a full genetic copy and capable of developing into an full organism.
Depending on which kind of alleles the parents pass down to the offspring will determine the offspring's genotype. The genotype of the offspring will, on the other hand, affect its phenotype which is the outward characteristic. An example is the sickle cell trait. If both gametes from the parents contribute the recessive alleles of the gene, then the offspring will be homozygous recessive for sickle cell genotype and this will show in the phenotype pf the person who will have sickle cell shaped blood cells.
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For more on genotype check out these;
brainly.com/question/11612019
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Answer:
CCAGGCC
CCATCGA
GGCCATC
CAT
AGGCCAT
CATCGAG
Explanation:
Shotgun sequencing is a method used to determine the nucleotide sequence of entire chromosomes/genomes. This sequencing method consists of obtaining random DNA fragments which are subsequently classified by bioinformatic tools that ordering them according to overlapping sequences called contigs. In the whole-genome shotgun (WGS) technique, the entire genome of an organism is sequenced, being the critical factor the depth of sequencing, which refers to the quality of the sequencing reads (e.g., a depth of 20X indicates that the genome is sequenced 20 times by a sequencing machine). For the human genome, WGS became available after the completion of the Human Genome Project (HGP), which enabled the generation of a reference sequence for the whole human genome. The steps of the WGS technique are the following:
1. Preparation of isolated chromosomes
2. The DNA is sheared into small fragments
3. The DNA fragments of about 1 kilobase (1000 base pairs) are incorporated into plasmids which are cloned to render pure samples of each DNA fragment
4. The plasmid clones are sequenced by sequencing machines
5. Bioinformatic tools finally are used to link DNA fragments by their overlapping ends