| Chromosome 6 specific sequencing libaries were created from the flow |
| sorted Coriell DNA NA11321 (Chinese origin). |
| We aligned the sequencing reads to build33 of the human genome, |
| available at ftp://ftp.ncbi.nih.gov/genomes/H_sapiens/, using ssahaSNP. |
| The settings for ssahaSNP were such that the candidate SNP base in the |
| read was at least Phred Q=23, that its neighbouring 5 bases on either |
| side of the candidate SNP all had Phred quality values of >=15 and at |
| least 9 of the 10 neighbours match. If the number of detected SNPs for |
| the aligned segment of a read exceeded a rate of 15 SNPs per 1000 bases |
| then that read alignment was ignored. If a read aligned to more than |
| one place in the genome, then only the longest alignment with the fewest |
| SNPs was reported. |
| Note: Flow sorting of chromosomes also includes a small percentage of |
| unintended chromosomal material. Therefore some reads for this flow |
| sorted library may generate SNPs on other chromosomes. |