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. 2013 May 14;14:330. doi: 10.1186/1471-2164-14-330

Table 4.

Highly differentiated SNPs validated with Sanger sequencing

Gene name Position in zebra finch genome Min reads/pool DI 454 DI Sanger S Sweden N Sweden/ S Sweden Lithuania
RNF6*
Chr1: 48,509,942
13
0.92
0.69/0.56
RB1*
Chr1: 56,558,186
9
1.00
0.81/0.50
ESD*
Chr1: 57,059,422
12
0.92
0.63/0.38
ESD*
Chr1: 57,059,472
11
0.91
0.75/0.43
XPOT
Chr1A: 32,952,256
10
0.94
0.19
ADCYAP1R1
Chr2: 3,348,189
8
0.92
0.00
RNMT
Chr2:101,951,215
13
0.93
0.19
RNMT
Chr2:101,951,219
12
0.92
0.13
BAI3
Chr3: 86,028,013
9
0.92
0.06
ENSTGUG00000005084*
Chr5: 3,850,065
18
0.91
0.88/0.88
FADS3*
Chr5: 6,375,371
30
0.95
0.88/0.94
FADS3*
Chr5: 6,375,565
25
0.96
0.94/0.94
FADS3*
Chr5: 6,375,583
22
0.96
0.75/0.69
SORD Chr10: 3,477,546 15 0.94 0.00

Of the 14 candidate SNPs identified by the transcriptome analyses, eight (*) showed high to moderate differentiation (DI > 0.6) between southern (N = 8) and northern Swedish samples (N = 8) when independently validated by Sanger sequencing. These eight SNPs also showed elevated DIs between southern Swedish and Lithuanian samples (N = 8). The SNP in ADCYAP1R1 could only be successfully genotyped in four southern and five northern Swedish samples in the validation set.