Is there any suitable tutorial for using IGV through commmand line?
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bandanaschapagain •
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Hi, I have mitochondrial DNA sequences bam files which are the output of the alignment to its references. I used bcftools to identify the variants. I am now advised to confirm about the variants manually. I am looking forward to know about the current methods to verify the identified variants in the vcf files. I highly appreciated any suggestions at this point.
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GenoMax
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bandanaschapagain •
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bandanaschapagain •
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Hi!
I suggest you to use IGV in order to take a look at your files for variant identification or visualization.
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rodolfo.peacewalker •
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Experimental verification is still done using sanger sequencing.