User: marcocassone

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Posts by marcocassone

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HOW can select MAF <0,01 in a VCF files without use ANNOVAR?
... HOW can select variations with MAF <0,01 in a VCF files without use ANNOVAR? I have problem with EXOME analysis when I create a VCF files i can't selection MAF<0,001 because ANNOVAR is a FAKE in Galaxy, what's kind of tool i can use ? ...
new mutations exac snp exome rare variant written 22 months ago by marcocassone0 • updated 22 months ago by Jennifer Hillman Jackson25k
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Answer: A: Empty VCF file returned by ANNOVAR on Galaxy
... Annovar don't fuction also with hg19 why? thanks ...
written 22 months ago by marcocassone0
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Answer: A: Annovar not Running Annotation on VCF
... Annovar in Galaxy.org don't function why? thanks VCF file empty ever ...
written 22 months ago by marcocassone0
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Answer: A: Annovar Annotate VCF tool - empty tabular file
... i have the same problem... please help me ...
written 22 months ago by marcocassone0
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Answer: A: Whole Exome Sequencing
... excuse me i am new here now i am starting to use bioinformatic tools for WGS and WES. How can I filter variants on the base the frequency allele of 1000 genome? ...
written 23 months ago by marcocassone0

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