Hi,
I had a query regarding the mitochondrial variant count for human samples. There was Exome + Mito panel sequencing data. I have mapped processed data against complete human genome then i have filtered out mito genome specific mapped reads (BAM) and gave input to Mity tool. The predicted variant count is around 50 to 100 across samples. Is this expected variant count?
Hi,
I had a query regarding the mitochondrial variant count for human samples. There was Exome + Mito panel sequencing data. I have mapped processed data against complete human genome then i have filtered out mito genome specific mapped reads (BAM) and gave input to Mity tool. The predicted variant count is around 50 to 100 across samples. Is this expected variant count?