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(7 intermediate revisions by 3 users not shown) |
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| GGGGYY | | GGGGYY |
| GGGYYY | | GGGYYY |
− | GGYYYR
| + | ? |
− | GYYYRR
| + | GGYYYR |
− | YYYRRO
| + | GYYYRR |
− | missing
| + | YYYRRO |
− | YRROOY
| + | missing |
− | missing
| + | YRROOY |
− | ROOYYG
| + | missing |
− | OOYYGG
| + | ROOYYG |
− | ?
| + | OOYYGG |
− | GGGGYR
| + | ? |
− | GYRK
| + | GGGGYR |
| + | GYRK |
| | | |
− | ---------------------------T3 Data---------------------
| + | KRROOYYGGGGGYYYGGGYYYRROOYYGGGGGGYRK <br> |
− | | + | based on mutagens, this seems only possibility left, would be happy if this was double checked. |
− | Aperio proposes this vine:
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | I found this note on Rauul's page:
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− | Rauul#1 (acts exactly like Amusement is a Light red)Amusement-Frivolity (7L chest)
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− | This interests me because it suggests that there was no impact on the tend table after a cross. That tells me that Frivolity's Color trait may be on the right splint and it's just sliding into the long G sequence. It also suggests that the trait information we have on Amusement's right splint is easy to replicate. I'm going to hammer it with milky trials and see what we get. -Aperio
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− | Calen solvent data
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− | YRK
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− | KRRO RROO ROOY GYYY YYGG KROO
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− | Have conflicting data here with two sets starting with 'K'
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− | OOYYG YGGGG YGGGY YYYRR YRROO RROOY ROOYY
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− | Aperio solvent data (200 trials)
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− | Just a comment - I've never identified a new triplet after 100 trials and most appear after 50. This number seems sufficient to establish what triplets are present. This vine was the exception to the 50 trial guideline.
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− | (21.5%) (43) GGG - 1111111111111111111111111111111111111111111
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− | (08.0%) (16) GGY - 1111111111111111
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− | (03.0%) (06) GYR - 111111
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− | (04.5%) (09) GYY - 111111111
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− | (05.5%) (11) KRR - 11111111111
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− | (05.0%) (10) OOY - 1111111111
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− | (06.0%) (12) OYY - 111111111111
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− | (06.0%) (12) ROO - 111111111111
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− | (06.0%) (12) RRO - 111111111111
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− | (10.0%) (20) YGG - 11111111111111111111
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− | (02.5%) (05) YRK - 11111
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− | (03.0%) (06) YRR - 111111
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− | (09.5%) (19) YYG - 1111111111111111111
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− | (03.5%) (07) YYR - 1111111
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− | (06.0%) (12) YYY - 111111111111
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− | Frequency bands appear to be +/- 1.5% from 4.5%, 9.0%, 22.5%
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− | YYY? YRR?
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− | YYR and YYG pair with GYY and OYY and YYY has to next in there somewhere
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− | GYR or YYR leads to YRK. The other leads to YRR
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− | KRR & YRR suggests a second RRO which necessitates a 2nd ROO which creates a 2nd OOY and OYY
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− | One - KRR YRK
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− | One - GYR GYY YRR YYR
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− | Probably Two - YYY
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− | Two (deduction) OOY OYY ROO RRO
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− | Two - GGY YGG YYG (Could be 3, the high KRR prohibits me from easily going to 1 lower frequency band for singles)
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− | Five - GGG
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− | Post-mortem - looking at the Vine Theory stuff, I'm inclined to think I've got most of this one right. - Aperio
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− | The A trait is probably represented by OOY and is expected to appear twice
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− | The C trait is probably represented by RR and is expected to appear twice
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− | The S trait is represented by YYY and is expected to appear twice
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− | ### Re-analysis Work-In-Progress
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− | Frequency bands appear to be +/- 1.5% from 4.0%, 8.0%, 20.0%
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− | * One - KRR YRK One - GYR GYY YRR YYR
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− | * Two - YYY OOY OYY ROO RRO GGY YGG YYG
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− | * Five - GGG ?
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− | ###
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− | GGY + GYR = GGYR x1
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− | GGY + GYY = GGYY x1
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− | YYG + YGG = YYGG x2
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− | OOY + OYY = OOYY x1
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− | RRO + ROO = RROO x1
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | KRR 1
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− | RRO 1
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− | RROO
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− | ROO 1
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− | ROOY
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− | OOY 1
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | RROOY
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | OOYYG
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− | OYY 1
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− | YYG 1
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− | YGG 1
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− | YYGG
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | YGGGG
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− | GGG 1
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− | GGG 2
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− | GGG 3
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− | GGG 4
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− | GGY 1
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− | GYY 1
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− | GYYY
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− | YYY 1
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− | YYY 2
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | YYYRR
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | YRROO
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− | OOY 2
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− | OYY 2
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− | YYG 2
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− | YGG 2
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− | GGG 5
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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− | YGGGY
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− | GGY 2
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− | GYR 1
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− | YRK 1
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− | KRROOYYGGGGGGYYYYRROOYYGGGYRK
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