Fields In The Vcf File
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10.1 years ago
#CHROM    POS    ID    REF    ALT    QUAL    FILTER    INFO    FORMAT    /home/output.bam
10    389659    .    T    C    4.13    .    DP=2;RPB=9.668049e-01;AF1=0.4999;AC1=1;DP4=0,1,0,1;MQ=42;FQ=4.93;PV4=1,1,1,1    GT:PL:GQ    0/1:32,0,35:31

what mean field "POS" it? what does this mean position? what the position is?

snp vcf • 3.5k views
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Can a file .vcf generate a SNP database?

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what is a "SNP database" a RDMS ? define "generate"

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yes, i will try to become a SNP database. generate == "be processed for". is there a journal / paper related with "snp database and vcf"? I'm sorry, I am still a beginner in learning in bioinformatics.

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ask a new question on biostars please.

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10.1 years ago

A variant must have a location in the genome. This location is denoted by the chromosome/contig (#CHROM column) and base position on it (POS column). Note that the position is 5', which is important mostly for indels, since this could otherwise be ambiguous. Have a read through the spec (this is a somewhat outdated version, but the principals are the same).

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