A diverse data set of whole human genomes are freely available for public use to enhance any genomic study or evaluate Complete Genomics data results and file formats. These include 69 DNA samples sequenced using our Standard Sequencing Service, which includes whole genome sequencing, mapping of the resulting reads to a human reference genome, comprehensive detection of variations, scoring, and in
ãªãªã¼ã¹ãé害æ å ±ãªã©ã®ãµã¼ãã¹ã®ãç¥ãã
ææ°ã®äººæ°ã¨ã³ããªã¼ã®é ä¿¡
å¦çãå®è¡ä¸ã§ã
j次ã®ããã¯ãã¼ã¯
kåã®ããã¯ãã¼ã¯
lãã¨ã§èªã
eã³ã¡ã³ãä¸è¦§ãéã
oãã¼ã¸ãéã
{{#tags}}- {{label}}
{{/tags}}