I don't know about the other tools you mention, but the Ensembl VEP needs the genomic coordinates of the variant as input. As far as I understand from the very limited information that the user provides (s)he doesn't have those .... :( Plus I don't know which genome (s)he is working with .... maybe one we don't have in Ensembl .....
Hi everyone,
I have two data :
SNP data:
pos_ start 14185,21066,26659....
pos_end 14185,,21066,26659....
genotype T
reference C
gen list data:
......
CDS from (5 sile): 1,1920,2205.....
CDS to (3 sile):1527,1777,2077.....
initiation codon : GTG,TTG,TTG Termination codon: CGA,CTG,CAT....
I want to know at the position of SNPs which were contained in gen list? where the position in the gene was mutated and the protein. How can I find that? I would appreciate if you could give some pointers.
1 answer
I would suggest that you convert your data into a format that can be used by snpEff, the Ensembl Variant Effect Predictor, or annovar and use one of those softwares to annotate your variants. Perl might be a good choice of language to do the conversion.
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Don't you have the absolute genomic coordinates of your SNPs?
I try to understand your question, but I find myself unable to do so. Could you please improve the formatting of your example files? It is not at all clear to me what your starting point is.
@Berl Overduin: I just only have a excel data. @Lars Juhl Jensen: could you show me how to insert the picture in the question? I want to insert the excel data.