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Thread | Thread Starter | Forum | Replies | Last Post |
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#1 |
Junior Member
Location: berkeley Join Date: Jan 2018
Posts: 6
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hi folks, I have 5 illumina sequencing fastq files. 1 is the parent and 4 are mutants. I alligned the sequence to the refenrence genome I have all the BAM bed etc etc files. I cleaned repetitive seq in the bam file with picard. what I would like to find are the variants (SNv and indels) that are present in each of the mutant strain but not in the parent. also I would like to have the variants just in the coding sequences. what program can I use?
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,080
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You need just step 1 from this tutorial since you only want SNv.
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#3 |
Junior Member
Location: berkeley Join Date: Jan 2018
Posts: 6
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isnt this command comparing a bam file to the reference genome? what I want are the SNV/indels present in the mutant strain but not in the control strain.
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#4 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 7,080
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You are identifying changes w.r.t. a reference and then comparing those results to get the difference between your control and mutant results.
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variants calling |
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