When I first got my results I was busily collecting my matches. I collected anything 5cMs and up. I guess I thought I'd miss something if I didn't. Sure, I could have, but now I am working with the larger segments and I wish I had done this when I began. I use GenomeMate Pro to catalog my matches and keep track of the kits I manage. Most of the time I have anything under 12 cM hidden when viewing the matches on each chromosome. I thought it would be a good project to tackle some of the larger segments. I wanted an easy way to see the larger matches across all of the chromosomes at the same time. Below is what I did using my paternal phased kit
- Run a Matching Segment report set where it only includes 20+ cM segments
- Paste the results into a spreadsheet
- Format with headers to your preference
- Set the sorts so it will sort by Chromosome and then by starting point
- Use the fill cell tool to group the ones which cover the same area
- Add a column on the far right of your Spreadsheet. This column will be used to identify whether the match or the match group is from the Paternal Grandfather or the Paternal Grandmother's lines.
How my chromosome, starting and ending position and segment size groups look minus any identifying info(GEDmatch #s email addresses cropped out of pic) |
I did the same thing using the paternal phased for my sister. Yesterday I printed the spreadsheets and put them in sheet protectors in a binder. Today I begin reviewing our largest unassigned segments. Technology is great, but I really do better if I have a printed paper to look at while searching over a pedigree chart rather than flipping back and forth from the chart to an actual spreadsheet or program. Just the way I'm wired I guess. I'd love to hear what has worked for others
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