You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
I've been trying to compare some variant calling methods to use on mitochondria NGS data.
I've seen that you test your pipeline with HG00119 and I was wondering if you had curated a set of high confidence variants from this or another 1000Genomes's individuals. I have not been able to find anything similar anywhere.
Thanks in advance,
María
The text was updated successfully, but these errors were encountered:
1000 Genomes consortium has also provided a phase 3 mtDNA variant call set (http://ftp.1000genomes.ebi.ac.uk/vol1/ftp/release/20130502/) you can use as comparison, although I am not aware of the quality control advised on that variant calling. We do not provide a curated set of MToolBox variants calls for 1000 Genomes at the moment, but we can definitely recommend to :
remove mtDNA variants showing strand bias, while keeping only variants supported by both strands
double check the alignment of variants occurring in homopolymeric stretches (also by visual inspection of the BAM alignment at IGV or similar tools) and remove suspicious ones due to alignment / sequencing errors
set a sensible heteroplasmy threshold cutoff, tuned on sequencing metrics (e.g. read depth)
perform haplogroup prediction and compare predictions generated with different tools, e.g. MToolBox and Haplogrep2, to make sure they match and flag samples with discordant predictions. Discordant predictions might be the result of poor quality of the sequencing or to low mtDNA coverage leading to few informative SNPs available for prediction. Samples with multiple MToolBox haplogroup predictions are usually also indicative of a poor sequencing quality or low coverage.
Hi,
I've been trying to compare some variant calling methods to use on mitochondria NGS data.
I've seen that you test your pipeline with HG00119 and I was wondering if you had curated a set of high confidence variants from this or another 1000Genomes's individuals. I have not been able to find anything similar anywhere.
Thanks in advance,
María
The text was updated successfully, but these errors were encountered: