Finishing the euchromatic sequence of the human genome

人类基因组 基因组 编码 常染色质 遗传学 基因组计划 全基因组测序 参考基因组 生物 序列(生物学) 完整序列 基因 计算生物学 基因组进化 染色体 异染色质
作者
Uma Maheswari,Kamel Jabbari,Jean‐Louis Petit,Betina M. Porcel,Andrew E. Allen,Jean‐Paul Cadoret,Alessandra De Martino,Marc Heijde,Raymond Kaas,Julie La Roche,Pascal Lopez,Véronique Martin-Jézéquel,Agnès Meichenin,Thomas Möck,Micaela S. Parker,Assaf Vardi,E. Virginia Armbrust,Jean Weissenbach,Michaël Katinka,Chris Bowler
出处
期刊:Nature [Springer Nature]
卷期号:431 (7011): 931-945 被引量:4715
标识
DOI:10.1038/nature03001
摘要

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers approximately 99% of the euchromatic genome and is accurate to an error rate of approximately 1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human genome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead.

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