Human Genomics Flashcards

(9 cards)

1
Q

What is genomic sequencing?

A

A process in which the order of the nucleotide bases along an organism’s genome is determined

A genome consists of genes and other DNA sequences that do not code for proteins.

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2
Q

What can the sequence of nucleotide bases help identify?

A
  • Genes responsible for diseases
  • Genome sequences for conditions
  • Genomic mutations and variations

This identification is crucial for understanding genetic disorders.

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3
Q

What is the role of bioinformatics in genomic analysis?

A

To compare sequence data

Analysis of the human genome is one of the main achievements of bioinformatics.

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4
Q

What does the future of genomic analysis include?

A
  • Enhanced use of targeted drugs
  • Individualised therapy

A fuller understanding of how the human genome works is expected to lead to these advancements.

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5
Q

How has the cost and time of sequencing an individual’s genome changed?

A

Sequencing is now cheap, quick, and can be done in days rather than years

This advancement makes obtaining an individual’s personal genome relatively easy.

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6
Q

What can analysis of an individual’s genome predict?

A

The likelihood of certain diseases developing

This analysis can identify harmful or neutral mutations within the genome.

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7
Q

What is personalised medicine?

A

Medicine tailored to the individual based on their genomic analysis

It uses pharmacogenetics to predict the success of treatments.

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8
Q

What significant project was completed in 2003 related to the human genome?

A

The Human Genome Project

It sequenced three billion nucleotide bases and identified around 20,000 genes.

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9
Q

How can personalised medicine assist in treatment selection?

A

By selecting the best drugs and dosage for a patient’s particular disease

This approach increases the likelihood of treatment success.

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