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Ganezh [65]
3 years ago
11

Put the following processes in order from first to last.

Biology
2 answers:
soldi70 [24.7K]3 years ago
6 0

Answer:Ovulation—>Fertilization—>Implantation—->Birth

Explanation:the ovum is first released(ovulation) then a sperm merges with it (fertilization) the zygote is moved to the uterus(implantation) it grows to become a baby and the mother delivers it(birth)

cupoosta [38]3 years ago
4 0
Ovulation > fertilization > implantation > birth
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If the sequence of bases on one half of a DNA molecule is GATTACA, what is the sequence of bases on the opposite side (from left
AURORKA [14]
The sequence of bases on the other half of the DNA molecule would be CTAATGT from left to right, because each cytosine base pairs with a corresponding guanine base, and each adenine base pairs with a corresponding thymine base. 
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2 years ago
HELP!! DUE TODAY
goldenfox [79]

Answer:

In the past decade, genetic testing aimed at identifying ancestry has experienced exponential growth, with nearly 26 million tests sold since 2018 (6). Companies – such as 23andMe – offer kits to trace your genetic legacy and geographical origins using Y-chromosome, mitochondrial, and whole-genome markers (1). Genetic ancestry testing holds the potential to identify the geographic origins of an individual’s ancestors, ancestral lineages, and relatives, but does not define a deterministic cultural identity.

DNA located in the mitochondrion, mtDNA, is inherited maternally in both sexes and can thus provide evidence of an direct, unbroken female lineage (10). The mtDNA typically passes unchanged from mother to offspring, except in the rare case of a mutation. By comparing full mtDNA sequence or assaying for particular haplogroups, it is possible to establish both close ancestry and rough global origins, respectively (4). Regardless, two individuals, even with an exact mtDNA match, may have had an ancestor as far back as ten or sixteen generations (9). Consumers should thus be warned against over-interpreting mtDNA results since they unravel a single thread in an individual’s genetic ancestry. A distinct benefit of mtDNA tests is the ability to distinguish maternal lineage in recorded genealogical data in which females adopt the male surname (10).

Contrary to mtDNA, Y-chromosome DNA is inherited paternally, passed down from father to son. Ancestry tests analyze locations along the Y chromosome, cataloging mutations known as single nucleotide polymorphisms and repeating patterns known as short tandem repeats (8). Test results can determine if two male members of separate families with the same surname have a close genetic relationship (10). In addition, a multitude of haplogroups, representing branching in the Y-chromosome tree, can be used to examine the presence of a common ancestor thousands of years back, contributing another thread to the central question of genetic ancestry (8,7).

A more comprehensive basis of determining ancestry relies on the presence of millions of autosomal variants, such as single nucleotide variants (SNVs), across the genome (10,3,7). An individual’s unique pattern of SNVs is compared with various reference populations and other consumers in order to infer their ancestry (10). Companies such as 23andMe provide a readout of broad ancestry and specific subgroups. Ancestral populations such as European and Western Asian are often further broken down into subpopulations (e.g. British, Greek, Iran). The accuracy of more specific statistical inferences is often variable, with companies examining different SNVs reporting inconsistencies in percentages for the same individual (3). In addition, since many reference populations do not account for migration and interbreeding thousands of years back, an ethnicity estimate with a high degree of confidence could still differ drastically from an individual’s expectations (10). Statistical inferences have diminished accuracy in regions such as East Africa and South Asia with comparatively limited data relative to well studied European populations, leading to further possible inconsistencies (7).

While the commercialization of genetic-ancestry tests has resulted in improved accuracy and innovation, the hyper-aggressive marketing of such products risks misinforming consumers, particularly in regards to cultural heritage. Consider, for example, an advertisement by the company Ancestry where a woman finds “[her] strength” after realizing she shares maternal lineage to a matriarchal people in Ghana (11). The pervasive marketing has even infiltrated music: In 2018, Spotify and Ancestry partnered to suggest playlists and artists based on test results, blatantly equating DNA and cultural heritage (2). While such marketing efforts are externally harmless, they carry a hidden message that DNA plays a meaningful role in our cultural identity. Most consumers are ill-informed in the field of genomic science, and may assume that their test results are deterministic and connote a contribution to heritage.

Genetic-ancestry tests may also perpetuate the idea of innate racial differences and entangle race with culture. A randomized trial reported that White Americans with lower genetic literacy had increased essentialist views after receiving test results (6). Those of Hispanic heritage share cultural aspects such as language, but may differ in genetic test results due to post-colonial admixture of Native, European, and African populations (5). Does a test result of 90% European heritage indicate “more” Hispanic heritage than 80% African? Such conclusions are entirely inaccurate and dangerous, but plausible given the genetic literacy of the typical consumer.

Explanation:

8 0
3 years ago
Which one is larger a main sequence star or a neutron star
nevsk [136]
A main sequence star is bigger than a neutron star,because neutron stars are remnant degenerate matter from a collapsed star,they are completely made out of Neutrons and are extremely dense,and have a diameter of only a several Kilometers.M<span>ost of them have a mass of 1.35-2 Solar masses.</span>
3 0
3 years ago
What would be the answers for 33-34?
RUDIKE [14]

Answer:

chromosome

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6 0
2 years ago
2. If a cell has a very large amount of ribosomes attached to its rough
Otrada [13]

Answer:

Protein

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Ribosome and Rough E.R are organelles  in the cell.

E.R are extensive membranes (which are continuous with the nuclear membrane) that exist as flattened compartment in the cytoplasm.These compartment form sacs in the cytoplasm. The sacs are interconnected with one another to form a complete system  called the reticulum.

Based on structure two types of E.R exists -the Smooth E.R and the Rough Endoplasmic reticulum.The later is called rough because of Ribosomes attached to its outer membrane. the smooth lacks ribosomes attachment on its outer membrane. Ribosomes are the site of Protein synthesis in the cell.

They are small in number and are made up of RNA and protein.Generally the protein  synthesised  in the Ribosomes,are moved into the sacs in the R.E.R,where they are modified.They are eventually budded off in vesicles which form the Golgi bodies

5 0
3 years ago
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