https://www.selleckchem.com/mTOR.html
We managed to identify 16 pathogenic variants in the examined genetic material (mtDNA) according to the ClinVar database. Conclusions In conclusion, we have outlined that off-target reads from targeted gene panel (TruSight One Sequencing Panel) may also be suitable for determining potentially pathogenic homoplasmic variants in mtDNA. We also described a simple pipeline based only on free tools available online. Introducing such a pipeline into a standard procedure of clinical units which carry out such research undoubtedly can extend the diagnostic
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