Entering edit mode
20 months ago
Genetics
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30
Hi All, I am first time trying to identify the RNA editing sites from (A TO I )changes.I have used GATK pipeline and at the very end when I have generated raw_snps filtered annotation file by snpEff tool,the info column looks like this .I am not sure why in this info column showing two/three genes. I am not able to understand where I did the mistake.
AC=1;AF=0.500;AN=2;BaseQRankSum=-1.834;DP=16;ExcessHet=0.0000;FS=0.000;MLEAC=1;MLEAF=0.500;MQ=60.00;MQRankSum=0.000;QD=3.19;ReadPosRankSum=-2.499;SOR=0.105;ANN=A|splice_donor_variant&intron_variant|HIGH|EXON_supercont1.1_10978_11929|gene:MVLG_00003|transcript|transcript:MVLG_00003T0|protein_coding|3/7|c.137+1G>T||||||WARNING_TRANSCRIPT_NO_STOP_CODON,A|upstream_gene_variant|MODIFIER|EXON_supercont1.1_13591_13831|gene:MVLG_00004|transcript|transcript:MVLG_00004T0|protein_coding||c.-681C>A|||||565|WARNING_TRANSCRIPT_NO_STOP_CODON,A|upstream_gene_variant|MODIFIER|EXON_supercont1.1_15696_15743|gene:MVLG_00005|transcript|transcript:MVLG_00005T0|protein_coding||c.-2704C>A|||||2670|WARNING_TRANSCRIPT_NO_STOP_CODON,A|downstream_gene_variant|MODIFIER|EXON_supercont1.1_8132_8438|gene:MVLG_00002|transcript|transcript:MVLG_00002T0|protein_coding||c.*2144C>A|||||1953|WARNING_TRANSCRIPT_NO_STOP_CODON;LOF=(EXON_supercont1.1_10978_11929|gene:MVLG_00003|1|1.00
Thank you so much for your reply. In this case how could I able to identify where the actual editing occured because for the above example the vcf file is showing that at this "13026 " position C(REF) to A(ALT) changes occured but when I checked the MVLG_00003 exon I didnt find "C" at that position.In that case how do I know in which gene among the four(MVLG_00002,MVLG_00003,MVLG_00004,MVLG_00005) actually the editing happened?
which genome is it ? which build ?
This is genome of Microbotryum violaceum(fungi) https://fungi.ensembl.org/Microbotryum_violaceum/Info/Index
and I got a C at this genomic position.
Thank you.I was trying to see manually.
When there is more than one annotation at a perticular RNA editing sites,how do you know in which gene the editing happened? I have used "ud 0 " at the time of database creation using snpEff,but still getting samething.