What is Sanger sequencing? Why do we use ddNTP? How to read a DNA sequence gel? c. What is a cDNA seq (RNA seq)? d. What is the main difference between a genomic and a transcriptome study?

Q: a. What are the purposes of sequence alignment?

A: Sequence alignment is a method by which one can arrange sequences of DNA, RNA and protein so as to…

Q: The in situ hybridization method is based on Select one: a. labeling specific neuronal components…

A: Hybridization is the property of single-stranded nucleic acids to base-pair with their complementary…

Q: About transcriptomics and genomics, answer: 4. Can we replicate RNA? How can we use PCR and Sanger…

A: (a)RNA viruses can replicate their RNA. RNA can store and replicate genetic information. RNA…

Q: Besides the great potential of gene editing, what are the biggest risks?  How do scientist test to…

A: Gene editing is a rapidly advancing field of genetic engineering that allows for precise…

Q: How can I develop a vector to express a bacterial gene (2,500 bp in size) in E. coli. How do I know…

A: Hi! As you have posted multiple questions, I will be answering the first two questions for you. If…

Q: How is ribotyping similar to rRNA sequence analysis? How do the two techniques differ? Do you think…

A: RFLP is a method to check genetic markers in the genome of organisms. The genetic markers are…

Q: Within genomics, genetic engineering and gene therapy are two topics that are quite comparable. What…

A: Genomics is the study of an organism's entire genetic complement (the genome). It sequences,…

Q: Exaplain the two methods to study the contents of transcriptomes which are microarray analysis and…

A: Transcriptome analysis may be used to find novel genes and isoforms that are not already cataloged…

Q: DNA microarrays ... Select an answer and submit. For keyboard navigation, use the up/dow select an…

A: The principle behind DNA microarrays is that complementary sequences bind to each other. The…

Q: Site directed mutagenesis is used to: 1.determine the critical base per sequences in a Genome 2.…

A: DNA consists of double strands of sequentially arranged nucleotides. The nucleotide sequence present…

Q: How can we use the transposon sequence to find where the mutation occurred in a forward genetic…

A: Forward genetic screes, also termed as forwarding genetics, is a kind of process by which those…

Q: Check all the statements that are TRUE regarding 16S or ITS (microbiome) illumina (NGS) sequencing…

A: The Illumina sequencing chemistry is extremely precise, with the great majority of bases scoring Q30…

Q: Discuss the processes of conjugation, transformation (Griffith’s experiment), andtransduction. What…

A: Genetics is a branch of science that deals in the study of genes, heredity, and genetic variation of…

Q: oth microarray and RNA-sequencing can study the transcriptomes. Compare microarray and RNA…

A: Microarray is based on hybridization while RNA sequencing includes cloning and sequencing.…

Q: The temperature at which the primers and target DNA hybridize may be changed to influence the…

A: Introduction Temperature changes have an impact on the response, which may be noticed at both high…

Q: What is CRISPR? Give two applications for this technology.

A: CRISPR, which stands for Clustered Regularly Interspaced Short Palindromic Repeats, is a family of…

Q: How have GWAS's changed the field of genomics and what do they allow that other methods do not? What…

A: Introduction :- Genomics is a field of biology that focuses on the study of the structure, function,…

Genome annotation

The technique of linking biological information to genome sequences is termed genome annotation. Gene annotation is the method of identifying gene locations and coding sections. It helps us understand what these genes are doing in the body through establishing structural characteristics and linking them to the actions of various proteins.