| Submitter Method Handle: | HGSV | | Submitter Method ID: | NA18507-FOSMIDS | | Submitted method description: | |
| | This submission represents alignment of the fosmid end sequence from NA18507, Agencourt library_id ABC8, to build35 of the human genome, available at ftp://ftp.ncbi.nih.gov/genomes/H_sapiens/, using ssahaSNP. The settings for ssahaSNP were such that the c | | | 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. |
This method was used in the following submission:
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