Comments (8)
I just extracted the data from the zip file. I was not sure whether it is correct
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Did you check the output file? The output is written to the file ifit_hg38_bin_annovar.hg38_multianno.txt
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On Mon, Aug 26, 2024 at 10:54 PM fanwayne @.> wrote: table_annovar.pl ifit_hg38_bin.vcf $HOME/../../mnt/d/BaiduSyncdisk/biodata/humandb/ -buildver hg38 -out ifit_hg38_bin_annovar -remove -protocol refGene,ensGene,1000g2015aug_eas -operation g,g,f -nastring . -xref ~/annovar/example/gene_fullxref.txt -vcfinput My code was shown above. This running code did not prompt any errors or warning. But I just got nothing after running this code. Could you please help me with this issue? Many thanks! screenshot20240827105324.png (view on web) https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 — Reply to this email directly, view it on GitHub <#251>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY . You are receiving this because you are subscribed to this thread.Message ID: @.>
Yes, the field was all missing.
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Did you check the output file? The output is written to the file ifit_hg38_bin_annovar.hg38_multianno.txt
…
On Mon, Aug 26, 2024 at 10:54 PM fanwayne @.> wrote: table_annovar.pl ifit_hg38_bin.vcf $HOME/../../mnt/d/BaiduSyncdisk/biodata/humandb/ -buildver hg38 -out ifit_hg38_bin_annovar -remove -protocol refGene,ensGene,1000g2015aug_eas -operation g,g,f -nastring . -xref ~/annovar/example/gene_fullxref.txt -vcfinput My code was shown above. This running code did not prompt any errors or warning. But I just got nothing after running this code. Could you please help me with this issue? Many thanks! screenshot20240827105324.png (view on web) https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 — Reply to this email directly, view it on GitHub <#251>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY . You are receiving this because you are subscribed to this thread.Message ID: @.>
Oh, sorry, I'm afraid I checked the wrong file. I noticed that the text file has already been annotated, but the vcf file was not.
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VCF should be annotated as well, it is a new VCF file, not the original input.
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On Mon, Aug 26, 2024 at 11:14 PM fanwayne @.> wrote: Did you check the output file? The output is written to the file ifit_hg38_bin_annovar.hg38_multianno.txt … <#m_-3291927269789100615_> On Mon, Aug 26, 2024 at 10:54 PM fanwayne @.> wrote: table_annovar.pl http://table_annovar.pl ifit_hg38_bin.vcf $HOME/../../mnt/d/BaiduSyncdisk/biodata/humandb/ -buildver hg38 -out ifit_hg38_bin_annovar -remove -protocol refGene,ensGene,1000g2015aug_eas -operation g,g,f -nastring . -xref ~/annovar/example/gene_fullxref.txt -vcfinput My code was shown above. This running code did not prompt any errors or warning. But I just got nothing after running this code. Could you please help me with this issue? Many thanks! screenshot20240827105324.png (view on web) https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 — Reply to this email directly, view it on GitHub <#251 <#251>>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY . You are receiving this because you are subscribed to this thread.Message ID: @.> Oh, sorry, I'm afraid I checked the wrong file. I noticed that the text file has already been annotated, but the vcf file was not. — Reply to this email directly, view it on GitHub <#251 (comment)>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OGEZP56JXYUAK6YBVDZTPVLFAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43OSLTON2WKQ3PNVWWK3TUHMZDGMJRGQ4DKOBTGA . You are receiving this because you commented.Message ID: @.**>
Sorry. I rechecked the vcf file. Yes, the vcf file was also annotated. As only 2.1% of input SNPs was annotated with allele frequency by the 1000g2015 database, it looks like the majority were all missing.
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you should use gnomad to annotate allele frequency
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On Mon, Aug 26, 2024 at 11:57 PM fanwayne @.> wrote: VCF should be annotated as well, it is a new VCF file, not the original input. … <#m_-8093207385278309306_> On Mon, Aug 26, 2024 at 11:14 PM fanwayne @.> wrote: Did you check the output file? The output is written to the file ifit_hg38_bin_annovar.hg38_multianno.txt … <#m_-3291927269789100615_> On Mon, Aug 26, 2024 at 10:54 PM fanwayne @.> wrote: table_annovar.pl http://table_annovar.pl http://table_annovar.pl http://table_annovar.pl ifit_hg38_bin.vcf $HOME/../../mnt/d/BaiduSyncdisk/biodata/humandb/ -buildver hg38 -out ifit_hg38_bin_annovar -remove -protocol refGene,ensGene,1000g2015aug_eas -operation g,g,f -nastring . -xref ~/annovar/example/gene_fullxref.txt -vcfinput My code was shown above. This running code did not prompt any errors or warning. But I just got nothing after running this code. Could you please help me with this issue? Many thanks! screenshot20240827105324.png (view on web) https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 https://github.com/user-attachments/assets/442f3e62-8863-4317-a104-1ef62df72b55 — Reply to this email directly, view it on GitHub <#251 <#251> <#251 <#251>>>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY https://github.com/notifications/unsubscribe-auth/ABNG3OCUMRFPQ2ZMYPS4CUTZTPS5RAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43ASLTON2WKOZSGQ4DQMJUG4ZDKNY . You are receiving this because you are subscribed to this thread.Message ID: @.> Oh, sorry, I'm afraid I checked the wrong file. I noticed that the text file has already been annotated, but the vcf file was not. — Reply to this email directly, view it on GitHub <#251 (comment) <#251 (comment)>>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OGEZP56JXYUAK6YBVDZTPVLFAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43OSLTON2WKQ3PNVWWK3TUHMZDGMJRGQ4DKOBTGA https://github.com/notifications/unsubscribe-auth/ABNG3OGEZP56JXYUAK6YBVDZTPVLFAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43OSLTON2WKQ3PNVWWK3TUHMZDGMJRGQ4DKOBTGA . You are receiving this because you commented.Message ID: @.> Sorry. I rechecked the vcf file. Yes, the vcf file was also annotated. As only 2.1% of input SNPs was annotated with allele frequency by the 1000g2015 database, it looks like the majority were all missing. — Reply to this email directly, view it on GitHub <#251 (comment)>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABNG3OAFJBA2Y3Q5CBVEFB3ZTP2MDAVCNFSM6AAAAABNFFUUD6VHI2DSMVQWIX3LMV43OSLTON2WKQ3PNVWWK3TUHMZDGMJRGUZDAOBVG4 . You are receiving this because you commented.Message ID: @.**>
Thank you very much. yes gnomad showed more non-missing values.
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Related Issues (20)
- Downloading annotation database ....Failed HOT 4
- multianno.txt to multianno.vcf HOT 1
- Annotation of double base substitutions (DBS,DNP) HOT 5
- prepare_annovar_user.pl not working with COSMIC version 99 HOT 2
- Download hg38 Gnomad DB HOT 1
- Truncated VCF output at chr21 HOT 2
- Dbnsfp33 running time HOT 3
- Any plan to add All of US population frequency data as annotation source HOT 3
- prefix.exonic_variant_function is empty HOT 1
- Update gnomAD database to v4.1 in ANNOVAR (some issues in v4.0)
- index the dbfile by python
- strand error assignment HOT 1
- base substitution I input is inconsistent with the calling result
- Error for annotating chromosome and bp by rsID
- the base of AAChange.refGene is inconsistent with Ref/Alt HOT 2
- one locus match two different transcripts of the same gene HOT 2
- Please updata prepare_annovar_user.pl for clinvar_20240902.vcf.gz HOT 6
- how can I download /humandb/hg19_ALL.sites.2014_10.txt file througth ANNOVAR HOT 1
- Error: invalid dbstrand information
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