Open huangl07 opened 2 years ago
I have this question, too. But I guess it means that the data must be biallelic.
Yep, that’s correct.
-Zachary
Le ven. 17 juin 2022 à 11:34 AM, Chen Shuanghui @.***> a écrit :
I have this question, too. But I guess it means that the data must be biallelic.
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while I have already check my file , it is biallelic varaint
you may check the file ,thankyou sca10010-1.vcf.gz sca10010-2.vcf.gz
how ever when I filtered all missing variant, the error is gone!
I think there could be fixed ?
but why the calculated can not do with the missing allele?
Hello,
Selscan does not currently support missing data entries. So you will need to either filter/impute your loci with missing data in order to run the program.
Zachary
Le dim. 19 juin 2022 à 9:40 PM, huangl07 @.***> a écrit :
how ever when I filtered all missing variant, the error is gone!
I think there could be fixed ?
but why the calculated can not do with the missing allele?
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Thank you for your replay!
Hello,
This is correct that missing data is not currently supported.
-Zachary
Le ven. 17 juin 2022 à 3:19 AM, huangl07 @.***> a écrit :
hello xpehh users,how to understanc alleles must be coded 0/1 only?
does it means no missing in ref vcfs?
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Can you share the filtered code?
This error still exists
ERROR: Haplotypes from test1.vcf.gz and test2.vcf.gz do not have the same number of loci. Does that mean we need to keep the same number of loci
Hello,
Yes this is correct, the two vcf (or other format) files you pass should have the same loci in each file.
-Zachary
Le jeu. 15 déc. 2022 à 9:23 AM, original10012 @.***> a écrit :
ERROR: Haplotypes from test1.vcf.gz and test2.vcf.gz do not have the same number of loci. Does that mean we need to keep the same number of loci
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Hello, Yes this is correct, the two vcf (or other format) files you pass should have the same loci in each file. … -Zachary Le jeu. 15 déc. 2022 à 9:23 AM, original10012 @.> a écrit : ERROR: Haplotypes from test1.vcf.gz and test2.vcf.gz do not have the same number of loci. Does that mean we need to keep the same number of loci — Reply to this email directly, view it on GitHub <#85 (comment)>, or unsubscribe https://github.com/notifications/unsubscribe-auth/ABAKRQXT6EG3PILR23E4MBDWNMSUXANCNFSM5ZBKQ7GA . You are receiving this because you commented.Message ID: @.>
Thank you for your reply. I have successfully solved this problem.
hello xpehh users,how to understanc alleles must be coded 0/1 only?
does it means no missing in ref vcfs?