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The basics of choosing genetic research paper topics

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20 Genetics Research Paper Topics on the Science in the 21st Century

12 Facts on Genetics in the 21st Century for a Research Paper
Recommended genetic research paper topics
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Is probably one of the newest advances in genetics research and will provide a fertile area for research. This topic will require an investigation into any link between genes and homosexuality.

This topic will require you to research on the role played by technology; more specifically you could decide to write about:. Under this topic you will research the genetic causes of various types of cancer such as Breast cancer, Prostate cancer etc.

This topic is extremely relevant in raising awareness on possible preventive measures in dealing with cancer. This topic will require that you investigate the genetic causes of disorders that affect the nervous system such as:.

This topic has a long history of ethical debate and would require you to take a position for or against it. You could also decide to evaluate both sides of the argument. Under this topic, you will have to research on advances in the field of stem cell research and its application. This topic will require you to analyze genetic development throughout history with a focus on how human beings evolved.

It will require an analysis of what changed in human genetics over the years. These proteins are aggregated as spheroidal particles along the DNA strand which is coiled around each particle and forms a complex body known as nucleosome or v- body Fig. Each nucleosome is made up of four pairs of histones which are arranged in two symmetrical groups.

Non-histone proteins are acidic and form many enzymes, e. For cytogenetic study of chromosomes, cells are chosen which grow and divide rapidly in culture. The most commonly used tissues are skin, bone marrow and peripheral blood. Colchicine arrests the cell division at metaphase, by preventing the formation of microtubules of achromatic spindle.

At metaphase, the chromatids united by centromeres are maximally contracted. Hypotonic solution of sodium citrate is added to the cells and incubated for about 20 minutes. Now fixatives of mixture of ethanol and acetic acid are added to the pellet of cells, and are gently shaken to form a cell suspension. The slides are allowed to dry at room temperature. These Q- banding patterns fluorescent are unique for each chromosome. The enzymes are capable of denaturing the protein in the chromosomes.

The interband regions are rich in G-C base pairs. The R-binding is complementary to G-binding. The C-banding is, however, not evident in Y chromosome. It is a process of arranging the chromosomes in order.

Individual chromosomes are identified according to their length, position of centromere, length-ratio between their arms and presence of satellite bodies on their arms. It includes pairs of 1, 2, 3 chromosomes. Each of them is long and metacentric. It consists of pairs of 4 and 5 chromosomes, which are fairly long with sub- metacentric centromeres.

Most of them are of medium size and sub-metacentric. All of them are medium sized and acrocentric. It includes 21 and 22 pairs of chromosomes; Y chromosome belongs to this group. The distal ends of long arms of Y chromosome present fluorescent bodies after staining with a flurochrome dye. Five chromosome pairs comprising 13, 14, 15, 21, 22 possess satellite bodies; hence called sat-ch.

The autosomal marker traits include the blood groups and certain serum proteins. The X-linked marker traits include colour-blindness, the Xg blood group and in some cases glucose- 6-phosphate dehydrogenase deficiency. Restriction enzymes divide the DNA into fragments of variable length by cutting between the specific sequence of bases, the sites of which are different for different enzymes.

About 50,, genes are estimated to be present in the total human genome with 3 billion base pairs. As of early , over loci have been assigned to specific positions on the human genetic map. Abnormalities of about of these genes have been linked to human diseases.

Some of the important gene localisation on autosomes are placed herewith. Due to genetic defect of Y chromosome, the mullerian system becomes unresponsive to the effects of male hormones liberated by the foetal testes. Therefore, Y chromosome presents potent male determining genes, irrespective of number of X chromosomes. In addition to male determining genes, Y chromosome contains genes for hairy pinna and H-Y histocompatibility antigen.

The length of Y chromosome varies from person to person and follows the principle of Mendelism. Due to the presence of H-Y antigen, male grafts are occasionally rejected by females of the same strain. A normal female possesses XX chromosome constitution. In early embryogenesis both X chromosomes are genetically active and induce the development of ovaries. Foetal ovaries do not secrete any hormone. This rare inheritance is possible in an individual due to cross-over in gametogenesis on the paternal side.

Interstital deletion resulting from two breaks is followed by a union of the broken ends. The genes are not lost but placed in altered loci. The resulting chromosomes derived from transverse splitting of the centromere are known as iso-chromo- somes.

The manifestation of ring chromosome depends on the deletion of specific genes. Therefore, karyotype of this disease is-t 9; 22 q34; ql 1. Diagonal line across the chromosomes or their number indicates mosaicism, eg. Considered from molecular level, one pair of allelic genes regulates synthesis of one polypeptide chain.

When allelic genes regulating a particular character or trait, say height, work in the same direction both tall or both short , they are called homozygous; when working in opposite direction one tall and the other short , the alleles are heterozygous. It has been established in by Wilkins, Watson, and Crick on X-Ray diffraction that the DNA molecule is composed of two strands of polynucleotides arranged in a double helix. Purine bases include adenine A and guanine G ; pyrimidine bases include thymine T and cytosine C.

However, when the bases are in enol form, adenine may pair with cytosine and guanine with thymine. If the base sequence of one strand is known, the base composition of the other strand can be formulated. Sequence of bases and number of nucleotides of DNA are specific, and are different in different genes.

Thus innumerable forms of DNA exist in the genes and store diverse genetic information. The ribosomes are the sites where polypeptide chains of proteins are formed by the linear linkage of different amino acids. Twenty 20 amino acids are involved in the biosynthesis of proteins. This is where the name came from. In this procedure, you can choose the gender of your child and prevent any kind of inherited diseases or other genetic defects from happening.

Biologists have considered it NLF new life form , classifying it as a 4th domain of life. Do you know why some people are capable of fighting off malaria easily while some are immune to severe symptoms of this illness? However, this mutation is an adaptive advantage only if one of the two alleles of sickle-cell disease are found in a person. In , when one person had gotten trapped in a car accident, an important genetic discovery was made.

This is because so-called victim involved in the car crash barely had any kind of fracture in his bones. Through the wisdom of human genome, it was found that he actually had a genetic mutation which caused his bones density to be eight times higher than an average male of his age. When an extensive study was conducted, it was found that there are other families that had denser bones than average and never had a broken bone in their life.

If you have hated the taste of brassica genus plants like broccoli or cabbage then there may be a scientific reason to it. A research has revealed that some vegetables contain identical chemical similarities to phenylthiocarbamide PTC , which is a chemical that is either tasteless or tastes a bit bitter, depending on the genetic makeup of a person.

Did you know that bananas were multi-seed fruits that were not as readily edible? Humans have interceded in changing the flavor and texture of bananas by crossing two kinds of this fruit: This resulted in a soft texture and irresistible flavor whereas the original fruit was rather unappetizing and had a hard feel and texture to it.

This genetic mutation was dubbed CCR5-Delta


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Genetics Genetics research papers examine the study of genes and how they relate to heredity and variation in living organisms. Genetics is a relatively new biological field that includes the study of genes and how they relate to .

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Jun 26,  · Various Genetic Disorders Alterations in human chromosomes or the deletion of an important gene product are often due to a mutation, which can spring an abundant strand of genetic mutations and improper coding.

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ADVERTISEMENTS: Here is your research paper on human genetics, chromosomes and genes! We inherit some physical and biochemical characters from our parents and ancestors. Transmission of inherited characters or traits through generations is known as the heredity. Genetics is that branch of bioscience which deals with the study of the . Research within librarian-selected research topics on Genetics from the Questia online library, including full-text online books, academic .

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See our collection of genetics research paper examples.. These example papers are to help you understanding how to write this type of written assignments. Genetics is the study of genes, genetic variation, and heredity in living organisms. Research on genetics in the 21 st century has led to many health advancements by sharing the wisdom and know-how of different areas of medicine. In this second guide, you will find 20 genetics research paper topics to give you an edge over your classmates. These topics are thorough, catchy and informative, which are necessary attributes of a topic in a research paper.