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. Author manuscript; available in PMC: 2014 May 28.
Published in final edited form as: N Engl J Med. 2010 Mar 10;362(13):1181–1191. doi: 10.1056/NEJMoa0908094

Table 3.

Individual Human Genomes Sequenced to Date.*

Genome Technology Used Average Depth of Coverage SNPs
Total Known Novel

×10−6

Venter Sanger method     7.5 3.21 2.80 0.74

Watson 454 Sequencing System (Roche)     7.4 3.32 2.71 0.61

Chinese (YH) Genome Analyzer (Illumina) 36 3.07 2.67 0.39

African (NA18507) Genome Analyzer (Illumina)   40.6 3.61 2.72 0.88

African (NA18507) SOLiD system (Applied Biosystems)   17.9 3.86 3.13 0.73

Korean (SJK) Genome Analyzer (Illumina)     28.95 3.43 3.01 0.42

Korean (AK1) Genome Analyzer (Illumina)   27.8 3.45 2.88 0.57

Proband in this study SOLiD system (Applied Biosystems)   29.9 3.42 2.85 0.56
*

All genomes listed have a ploidy of 2n. SNP denotes single-nucleotide polymorphism.

The surname of the individual person or the ethnic group (and HapMap sample name, in parentheses) is given. The same African (Yoruban) sample NA18507 was sequenced twice, once with the use of the Genome Analyzer and once with the use of the SOLiD (Sequencing by Oligonucleotide Ligation and Detection) system.