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Sequence Analysis Tools for Molecular Biologists

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Assembling Sequences Using phrap

MacVector Assembler assembles sequences using the phrap algorithm. phrap does not require the sequences to have been base called by phred, or to have had any vector sequences masked. However, using phred and cross_match will improve the accuracy of phrap assemblies. phrap assembles sequences into contigs and creates a consensus sequence with its own set of quality values, based on the quality and strandedness of the overlapping sequences. Contigs can be viewed and edited in a contig editor that shows the aligned sequences along with the chromatograms in a lower pane. Clicking on a residue in the consensus sequence resets the chromatogram view so that they are all aligned to that base. This allows you to easily align the chromatograms so that you can resolve ambiguities in the consensus sequence.

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Clicking on a consensus residue

 

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You can select individual individual

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Overview

Creating a Sequencing Project

Base Calling Using phred

Vector Trimming with cross_match

Assembling Sequences using phrap

Editing and Analysis of Contigs

NGS Reference Assembly using Bowtie

NGS de novo Assembly using Velvet

Comparing Assembler and AssemblyLIgn

SplitFastqFile - a ultility to break up large fastq files.

Functional comparison with Sequencher