Rewrite the following sentences after correction. The variation in the length of tandem repeat of microsatellite DNA has serious translational affects as this is due to its coding region.Correct: If one parent has sickle cell anemia and other has carrier genotype than there is 25 % chance that any offspring is carrier.Correct: Sickled WBC block the flow of blood and Calcium as they stick together and caused by frame shift mutation.Correct: The N1303K mutation in the CFTR gene of CF patients is autosomal dominant disorder due to insertion of asparagine at 1303.Correct: If a person RBCs have B surface antigen and it will clump with antigen B such clumping indicates Blood type B.Correct: Indirect ELISA can detect polygenic gene expression.Correct:

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Rewrite the following sentences after correction. The variation in the length of tandem repeat of microsatellite DNA has serious translational affects as this is due to its coding region. Correct:

Biology Today and Tomorrow without Physiology (MindTap Course List)

5th Edition

ISBN:9781305117396

Author:Cecie Starr, Christine Evers, Lisa Starr

Publisher:Cecie Starr, Christine Evers, Lisa Starr

Chapter10: Biotechnology

Section: Chapter Questions

Problem 4DID

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Concept explainers

Hematology

Hematology is the branch of biology. Hematology is the medical field that deals with the treatment of blood disorders and cancers, such as hemophilia, leukemia, lymphoma, and sickle-cell anemia. Hematologists and hematopathologists are medical professionals who specialize in illnesses of the blood and its components.

Question

Rewrite the following sentences after correction.

The variation in the length of tandem repeat of microsatellite DNA has serious translational affects as this is due to its coding region.

Correct:

If one parent has sickle cell anemia and other has carrier genotype than there is 25 % chance that any offspring is carrier.

Correct:

Sickled WBC block the flow of blood and Calcium as they stick together and caused by frame shift mutation.

Correct:

The N1303K mutation in the CFTR gene of CF patients is autosomal dominant disorder due to insertion of asparagine at 1303.

Correct:

If a person RBCs have B surface antigen and it will clump with antigen B such clumping indicates Blood type B.

Correct:

Indirect ELISA can detect polygenic gene expression.

Correct:

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Question. Rewrite the following sentences after correction. (Subject: Biotechnology) The variation in the length of tandem repeat of microsatellite DNA has serious translational affects as this is due to its coding region. Correct: If one parent has sickle cell anemia and other has carrier genotype than there is 25 % chance that any offspring is carrier. Correct: Sickled WBC block the flow of blood and Calcium as they stick together and caused by frame shift mutation. Correct: The N1303K mutation in the CFTR gene of CF patients is autosomal dominant disorder due to insertion of asparagine at 1303. Correct: If a person RBCs have B surface antigen and it will clump with antigen B such clumping indicates Blood type B. Correct: Indirect ELISA can detect polygenic gene expression. Correct:
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how do i expand this into 1000 words The objective is to interpret the results of an RNA-Seq analysis to identify differentially expressed genes in breast cancer using figure 1. The data provided includes gene symbols, chromosome location, start and end points, strand, fold change, log2 fold change, p-value, and false discovery rate (FDR). The RNA-Seq analysis has identified several genes that are differentially expressed in breast cancer. These genes are located on various chromosomes and have varying levels of fold change, indicating the degree to which their expression levels differ between normal and cancerous cells. The gene with the highest fold change is EYA4, located on chromosome 6, with a fold change of 3604.4176. This indicates that the expression of this gene is over 3600 times higher in cancer cells compared to normal cells. The log2 fold change is 11.81555, which is a measure of the magnitude of the difference in gene expression. The p-value for this gene is extremely low…