KKI's SNP Analysis Tool is used to analyze Affymetrix (10K & 100K) SNP chip results from several perspectives. See options in Step 6 below.
The first line of the input file will be ignored, assuming it is a header line. The remaining lines of the input file are treated as data lines and contain the following eight tab-delimited columns, as shown below. Note that while some of the fields can be left blank, each data lines shall still contain seven tabs. KKISNP assumes the data lines had been sorted: first by Chromosome Number, followed by Chromosome Location.
| 1. SNP_ID |
|
| 2. Chromosome Number |
without prefixes like "chr", "chrom" |
| 3. Chromosomal Location |
USCS-GB track "Base Position" |
| 4. Call |
AA, BB, AB, or NoCall |
| 5. Copy Number |
USCS-GB track "CN" |
| 6. Significance of the Copy Number |
-/+log10(p-value) |
| 7. Meta Analysis Significance |
-/+log10(meta p-value) |
| 8. LOH |
UCSC-GB track "LOH" |
The consecutive homozygosity (AAs and BBs) segments will be searched and reported. A single NoCall between AAs and/or BBs is included as part of a consecutive homozygosity region. The "score" in the GFF output is the value of either Copy Number or LOH value times 100. While the track labeled "CN" shows the Copy Number values for each SNP, the track labeled "CNR" shows the averaged Copy Number value for each consecutive region.