Hello,
I am trying to map the human mitochondria genome and try to find large insertion/deletion (> larger than 10 bps). I have paired-end fastq file of mitochondria genome using NGS..
It is the first time for me to do it. Could you please let me know the procedure for it?
Maybe, I am thinking to download the mitochondria reference human genome. Using only this one (instead of whole genome references), use bowtie2 to map to the reference mitochondria genome., which leads to the bam file..
Than, using this bam file, what kind of program do I have to use to identify the large (>10bp) insertion and deletion.
Please help me with this!
Thank you Fidel.
I have run bowtie2 to map the mitochondria gene.
In this case, I have used whole genome fasta file and gtf file. (I am not sure whether it is right or not. I meant that I have to use only the mitochondria genome instead of whole genome for mapping..)
Here is the result of bowtie2 mapping. Could you please confirm for this?
.. duplicated post