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. 2004 May 3;101(19):7329–7334. doi: 10.1073/pnas.0401648101

Table 1. Assignment of supercontigs by chromosome.

Chromosome
Assigned supercontigs
Polymorphisms
Name Size, kb Sum, kb Count Coverage, % Count Per kilobase covered
chr R 2,530 1,743 22 68.9 6,198 3.56
chr 1 3,165 3,034 26 95.9 12,969 4.27
chr 2 2,300 1,989 18 86.5 8,681 4.36
chr 3 1,820 1,666 10 91.6 2,962 1.78
chr 4 1,700 1,485 15 87.4 6,854 4.61
chr 5 1,230 1,081 10 87.9 10,254 9.48
chr 6 1,090 902 12 82.7 6,720 7.45
chr 7 1,020 950 8 93.1 1,640 1.73
Subtotal 14,855 12,851 121 86.5 56,278 4.38
Conflicts 120 2 298 2.48
Unmapped 1,879 143 5,958 3.17
Total 14,855 14,851 266 100.0 62,534 4.21

The haploid supercontig set totals 14,855 kb, which is very close to the estimated haploid genome size derived from physical criteria. Chromosome sizes were calculated from the summation of Sfil fragments assigned to each. The actual size of chr R is ≈ 3.2 Mb; in the table, 700 kb was deducted for its rDNA cluster (measured as BamHI and Xhol fragments). The repeat is present only once in the assembly. The only significant difference from published maps relates to the Sfil fragments of chromosome 1 (24), where fragment J2 appears to be replaced by three small fragments. Also, some Sfil sites that are heterozygous in the mapping strain are absent or present on both homologs in SC5314. “Conflicts” gives statistics for the two PHRAP contigs that contained map markers from more than one chromosome; these contigs were passed unchanged into the diploid assembly. “Unmapped” refers to supercontigs not containing any map markers. Values in the table are rounded.