Comments (5)
Hello, and thank you for your interest in MANTIS. We have not tested it on WGS data, however it should function provided sufficient coverage. Could you post median coverage and quality statistics? This would assist in choosing thresholds.
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Hi @rbonneville,
we do have a similar question. We have some tumor/normal paired WGS data with median coverages of ~70-80x. Which other quality statistics do you need or is this sufficient to recommend parameters for MANTIS?
Thanks,
Clemens
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Hi @messersc, do you have any quality statistics, for instance %Q30?
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Hi @rbonneville, the runs look very good in general, the %Q30 is > 95 % for all libraries (this is paired-end, 151 bp data).
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Given the high %Q30 and your median coverages, I would recommend first trying whole exome parameters.
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Related Issues (20)
- MANTIS on Mouse samples HOT 3
- MANTIS output fails if path to output contains a dot and output file stem does not
- Microsatellite Loci BED File HOT 11
- Repeatfinder missing? HOT 1
- Issue running MANTIS HOT 12
- How to select MSI loci most predictive of a sample's status ?? HOT 2
- Remove the step of correct off-by-one error in MANTIS ?
- Issue in HOT 4
- Issue HOT 1
- Issue in runni HOT 1
- In README: make RepeatFinder
- interpreter mismatch HOT 2
- Failed to fetch sequence; Error with k-mer repeat count calculations; terminating program. HOT 5
- About MS loci BED file used in MANTIS HOT 1
- Is it possible that using MANTIS to analyze RNAseq data? HOT 2
- can't finish the process HOT 8
- Running Mantis on WGS Sample
- typo in module checking HOT 1
- Error with k-mer repeat count calculations; terminating program, which seems to be triggered by "_multiprocessing.SemLock Permission Denied" HOT 1
- Use the FASTA index to get chromosome ordering
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