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Obtain Population frequency of B allele Axiom_UKB_WCSG #36
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You can use compile_pfb.pl to generate his file yourself after you have all signal files.
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On Jan 30, 2019, at 5:25 PM, Nihir ***@***.***> wrote:
Hello Dr. Wang,
I am trying to use PennCNV with Axiom_UKB_WCSG array but no sure what is the right PFB file required in step 1.3 http://penncnv.openbioinformatics.org/en/latest/user-guide/affy/.
I checked file "Axiom_GW_HumanOrigin.hg38" provided with pennCNV but when I overlapped SNP IDs with the one in annotation files from Axio it only overlap 70K ids.
I have also downloaded a file (Axiom_UKB_WCSG.na35.af_supp.tab) from affemetrix website that contains allele frequencies from "1KGp1_mar2012 and Affymetrix_internal_screen". The file contains frequencies from various populations , below are few column names from header
Probe Set ID Affy SNP ID Freq_A ASW Freq_B ASW Heterozygosity ASW Number ASW Minor_Allele ASW MAF ASW Freq_A CEU Freq_B CEU
Is this the right file to obtain B allele frequencies for PBF file ?
Best,
Nick
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Dr. Wang, Best, |
I do not have experience on Axiom, but the instructions are on the website
based on other people's experience. You can just follow the instructions to
get signal data and normalize signal data and then use it. You should not
need to do any extraction yourself.
For PFB file, you can simply create one yourself, using 0.5 as the allele
frequency for all SNPs. The purpose is only to provide coordinate
information for SNPs. Later on, after you have all signal files, you can
then generate a more accurate PFB file for CNV calling.
…On Thu, Jan 31, 2019 at 8:44 AM Nihir ***@***.***> wrote:
Dr. Wang,
Thanks for quick reply , I read about script "compile_pfb.pl" but as you
stated, the script uses individual intensity files , which was explained in
documentation in step 1.2. However, in the step I couldn't find description
to generate the intensity files for Axiom data.
Should I extract signal intensity for each sample from
"AxiomGT1.summary.txt" generated in Step1?
Best,
Nick
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Thank you very much again for prompt reply. This is helpful, I understand how to proceed now. Best, |
Dr. Wang, I am working on Illumina 770k HD chip for 96 samples of cattle. I am not able to generate pfb files for my data as I am unable to get the idea of the exact structure input files. Please explain clearly. Also specify the minimum number of samples for which pfb file can be generated. How to generate hmm and GC model file for this data or the one given in the module can be used? |
Hello Dr. Wang,
I am trying to use PennCNV with Axiom_UKB_WCSG array but not sure which one is the right PFB file used in step 1.3 http://penncnv.openbioinformatics.org/en/latest/user-guide/affy/.
I checked file "Axiom_GW_HumanOrigin.hg38" provided with pennCNV but when I overlapped SNP IDs with the one in annotation files from Axio it only overlap 70K ids.
I have also downloaded a file (Axiom_UKB_WCSG.na35.af_supp.tab) from affemetrix website that contains allele frequencies from "1KGp1_mar2012 and Affymetrix_internal_screen". The file contains frequencies from various populations , below are few column names from header
Is this the right file to obtain B allele frequencies for PBF file ?
Best,
Nick
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