BLAST Results and Gene Analysis

BLAST Results and Gene Analysis

Assessment

Interactive Video

Biology, Science, Computers

11th Grade - University

Hard

Created by

Patricia Brown

FREE Resource

In this video tutorial, Kevin Tokeoff from Catalyst University explains how to analyze gene sequence results using the BLAST program. The tutorial covers obtaining gene sequences, preparing them for analysis, and using BLAST to verify and identify genes. It also discusses interpreting BLAST results, focusing on key metrics like XM numbers, identities, gaps, and expectation values to ensure accurate gene identification.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary function of the BLAST program?

To synthesize new proteins

To compare nucleotide sequences against a database

To sequence DNA from scratch

To edit gene sequences

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which company is mentioned as a common provider for gene sequencing results?

Gene Lab

Gene Tech

Gene Whiz

Gene Corp

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What should you do with the sequence ends that contain many 'N's?

Replace them with 'A's

Highlight them for further study

Leave them as they are

Remove them before analysis

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What does BLAST stand for?

Basic Linear Alignment Search Technique

Basic Local Alignment Search Tool

Biological Linear Analysis System Tool

Bioinformatics Linked Alignment Search Tool

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the significance of the XM number in BLAST results?

It represents the sequence's molecular weight

It shows the sequence's GC content

It is a unique sequence identifier

It indicates the sequence length

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the ideal expectation value (E-value) in BLAST results?

As high as possible

Exactly 0.5

Exactly 1

As low as possible

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why is it important to maximize identities in BLAST results?

To reduce the number of gaps

To increase the sequence length

To confirm the sequence matches the gene of interest

To ensure the sequence is unique

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