Mining SNPs From EST Databases

Table 3.

EST–SNPs Confirmed by Fluorescence-Based Sequencing

Contig EST–SNP sequence context Frequency
1 A A G C T G T G G C (C/T) A C A C C T T C C C 4/2
1 C T T C C C G C T C (G/C) T C T G C T G C T G 4/2
2 C C A T A A A T G C (G/A) C T A A G A T A A A 5/1
2 A A T T A A A G A A (C/T) A A T A A T G T T C 5/1
3 T T T T A A C A A A (G/C) T A A T C T T C A C 5/1
4 A T A A G A T T A T (T/A) A T A A T A T A T A 5/1
5 T T C A G T T T T G (A/T) G G C T C A T G G G 5/1
6 C A G T C T G T A T (C/T) T T C C A A A A A G 5/1
7 G A G T C G A A A T (G/C) T G A T T C T T C A 4/2
7 G A A T G C A G T C (C/T) G T C A T A T G A C 4/2
7 T G A C C A C T A A (C/T) T T G C A T G T G A 4/2
  • Summary of SNPs confirmed by fluorescent-based sequencing.

  • The contig sequences and their corresponding GenBank accession numbers can be found in the NCBI SNP database under the submitter handle debnick SNPS-981209-A and SNPS-981209-B.

  • More than one SNP per contig was confirmed in contigs 1, 2, and 7.

  • Context surrounding the substitution noted between parentheses (major allele/minor allele).

  • Total of six chromosomes sequenced (three individuals).

This Article

  1. Genome Res. 9: 167-174

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