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 »ùÇÿ䱸·® ¹× ³óµµ :
    1~2 ug ÀÌ»ó (»ùÇÃQC Æ÷ÇÔ),
    ³óµµ 50 ng/ul ÀÌ»ó

 Sample quality : 260/280 1.7 ÀÌ»ó
                        260/230 1.7 ÀÌ»ó
 Àü±â¿µµ¿½Ã Àý´ë ±úÁöÁö ¾ÊÀº »ùÇÃ
 Amplified sampleÀº º» Ç÷§Æû¿¡ ÀûÇÕÇÏÁö
 ¾Ê½À´Ï´Ù.
 »ùÇÿ䱸·® ¹× ³óµµ :
    1~2 ug ÀÌ»ó (»ùÇÃQC Æ÷ÇÔ),
    ³óµµ 50 ng/ul ÀÌ»ó

 Sample quality : 260/280 1.7 ÀÌ»ó
                        260/230 1.7 ÀÌ»ó
 Àü±â¿µµ¿½Ã ±úÁöÁö ¾ÊÀº »ùÇÃ
 Amplified sampleÀº º°µµ ¹®ÀÇ ¹Ù¶ø´Ï´Ù.
 

* Goldengate OPA (Oligo Pool Assay) Design

Goldengate customized chipÀ» Á¦ÀÛÇϱâ À§Çؼ­´Â ÀÏ´Ü ¿¬±¸ ¸ñÀû¿¡ ¸Â´Â candidate SNP list¸¦
¼±º°ÇÏ´Â °ÍÀÌ Áß¿äÇÕ´Ï´Ù. ÀϹÝÀûÀ¸·Î ¾Æ·¡¿Í °°Àº ±âÁØ¿¡ ÀÇÇÏ¿© candidate SNP list¸¦ ¼±Á¤Çϰí
ÀÖ½À´Ï´Ù. ¢ß¸¶Å©·ÎÁ¨¿¡¼­´Â °í°´ÀÇ OPA µðÁöÀÎ ¼­ºñ½º¸¦ Á¦°øÇϰí ÀÖ½À´Ï´Ù.

   Haplotype tagging SNPs (htSNPs)
   High heterozygosity (>0.1) & high MAF (>0.05)
   Moderate LD between SNPs (LD: 0.25~0.3Á¤µµ Àû´ç)
   SNPs in highly conserved regions of the gene
   SNPs previously studied
   SNPs identified by multiple submitters in multiple sites.

¸ÕÀú °í°´²²¼­ ¿¬±¸ ¸ñÀû¿¡ ¸Â´Â candidate SNP list¸¦ ¼±º°ÇÏ¿© rs#, sequence, gene, region
(physical position start-end) ÇüÅ·ΠÁ¦°øÇØ Áֽøé OPA Á¦ÀÛ °¡´É¿©ºÎ¸¦ ÆÇº°ÇÏ°Ô µË´Ï´Ù.
ÀÌ ÀÛ¾÷À» SNP scoring ÀÛ¾÷À̶ó°íµµ Çϴµ¥, illumina oligo probe Á¦ÀÛÀÌ °¡´ÉÇÑÁö ¿©ºÎ¸¦
SNP score·Î Á¡¼öÈ­ ½ÃŰ´Â °úÁ¤À» ¸»ÇÕ´Ï´Ù. ¿©±â¼­ SNP score¶õ 0~1.1 »çÀÌ °ªÀ¸·Î probe µðÀÚÀÎ
¼º°ø¿©ºÎ¸¦ ¾Ë·ÁÁִ ôµµÀÔ´Ï´Ù.
ÀϹÝÀûÀ¸·Î SNP score°¡ 0.6 ÀÌ»óÀÌ¸é ¼º°øÀûÀ¸·Î probe Á¦ÀÛÀÌ °¡´ÉÇÏ°Ô µË´Ï´Ù.
´ÙÀ½Àº SNP scoring ÁøÇà ´Ü°è¿¡¼­ ¹ß»ýÇÒ ¼ö ÀÖ´Â fail codeÀÔ´Ï´Ù. candidate SNP ¸ñ·ÏÀ» ÀÛ¼ºÇÒ ¶§
¾Æ·¡ÀÇ Ç׸ñÀ» °ËÅäÇÏ¿© ¼±Á¤Çϸé, º¸´Ù ½±°í ½Å¼ÓÇÏ°Ô OPA µðÀÚÀÎÀ» ¿Ï·áÇÒ ¼ö ÀÖ½À´Ï´Ù
Critical failures (undesignable)

   101= Flanking sequence is too short.
   102= SNP or sequence formatting error. SNP must match the format:[X/Y]
    Possible causes:
       - Spaces found in submitted sequence.
       - More than one set of brackets in sequence. Missing brackets around SNP
       - SNP alleles not separated by a ¡°/¡±
   103=Top/Bot strand cannot be determined. Low sequence complexity
   104=SNP is not appropriate for Illumina platform.
       Possible causes:
       - Tri- or quad-allelic SNP
       - Insertion or deletion polymorphism
       - SNP contains characters other than A, G, C, or T
   106=Degenerate nucleotide(s) in assay design region
       - e.g. W, R, S, N, etc.
Warnings (designable)

   301=SNP in duplicated/repetitive region
   302=Tm outside assay limits
   340=Another SNP in this list is equal to or less than 60 nucleotides away.
   399= Multiple contributing issues