Hi Jim,
I'm currently testing IGV for visualising SNPs on a bacterial genome. I've generated a SNP table with CLC which looks like this;
Reference Position Consensus Position Variation Type Length Reference Variants Allele Variations Frequencies Counts
122 122 SNP 1 G 1 A 100 133
1411 1411 SNP 1 T 1 C 100 135
1639 1639 SNP 1 G 1 A 100 127
1738 1738 SNP 1 A 1 G 100 118
....
I have converted this file to a simple .bed file;
GENOMENAME 121 122 A
GENOMENAME 1410 1411 C
GENOMENAME 1638 1639 A
GENOMENAME 1737 1738 G
......
This all works, as i can read in the file and visualize it along the genome. However, i want to add more information, like the 'Frequences' and 'Counts' column. These columns should be displayed if i scroll over a SNP.
How can i do this? How should the input look like?
Thanks for the help,
Boetsie
I'm currently testing IGV for visualising SNPs on a bacterial genome. I've generated a SNP table with CLC which looks like this;
Reference Position Consensus Position Variation Type Length Reference Variants Allele Variations Frequencies Counts
122 122 SNP 1 G 1 A 100 133
1411 1411 SNP 1 T 1 C 100 135
1639 1639 SNP 1 G 1 A 100 127
1738 1738 SNP 1 A 1 G 100 118
....
I have converted this file to a simple .bed file;
GENOMENAME 121 122 A
GENOMENAME 1410 1411 C
GENOMENAME 1638 1639 A
GENOMENAME 1737 1738 G
......
This all works, as i can read in the file and visualize it along the genome. However, i want to add more information, like the 'Frequences' and 'Counts' column. These columns should be displayed if i scroll over a SNP.
How can i do this? How should the input look like?
Thanks for the help,
Boetsie
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