OpenAI首席科学家Ilya:AGI的到来会是一场雪崩
纪录片《iHuman》
纪录片《iHuman》
🎈-停止观看色情片
🎈-停止自卫
🎈-设定目标
🎈-停止观看软色情内容
🎈-聚焦内在,而非外在
🎈-专注自己,而非女性
用支付宝扫码 天天有优惠
核污染水排放于8月24日下午正式开始。
这是人类灭亡于核的节奏。核污水排进海里,完全是对人类不负责的。
截至我所知的2021年9月,有许多免费的图片压缩软件可供使用,这些软件可以帮助您减小图片文件的大小,节省存储空间并更快地在网络上上传或下载图片。
刚把相机SD卡插上电脑,不小心按了键盘,等我一抬头已经正在删除。悲剧了。 然后在百度上搜索怎么恢复删除的数据, ...
A pangenome reference of 36 Chinese populations.PDF
Human genomics is witnessing an ongoing paradigm shift from a single reference sequence to a pangenome form, but populations of Asian ancestry are underrepresented. Here we present data from the first phase of the Chinese Pangenome Consortium, including a collection of 116 high-quality and haplotype-phased de novo assemblies based on 58 core samples representing 36 minority Chinese ethnic groups. With an average 30.65× high-fidelity long-read sequence coverage, an average contiguity N50 of more than 35.63 megabases and an average total size of 3.01 gigabases, the CPC core assemblies add 189 million base pairs of euchromatic polymorphic sequences and 1,367 protein-coding gene duplications to GRCh38. We identified 15.9 million small variants and 78,072 structural variants, of which 5.9 million small variants and 34,223 structural variants were not reported in a recently released pangenome reference1. The Chinese Pangenome Consortium data demonstrate a remarkable increase in the discovery of novel and missing sequences when individuals are included from underrepresented minority ethnic groups. The missing reference sequences were enriched with archaic-derived alleles and genes that confer essential functions related to keratinization, response to ultraviolet radiation, DNA repair, immunological responses and lifespan, implying great potential for shedding new light on human evolution and recovering missing heritability in complex disease mapping.
大清国人人有病!
什么病啊!
愚昧之病?
愚在何处啊!
被奴役者却以为自由着。
从来不知道平等为何物。
不知自爱且不懂爱人。
一句话。
奴才不知道自己是奴才!
这张真是AI画的神作了。 显卡3070生成图片还是太慢了。100批次,1个多小时才生成20张,1张神作,1张还 ...
A pangenome reference of 36 Chinese populations.PDF
Human genomics is witnessing an ongoing paradigm shift from a single reference sequence to a pangenome form, but populations of Asian ancestry are underrepresented. Here we present data from the first phase of the Chinese Pangenome Consortium, including a collection of 116 high-quality and haplotype-phased de novo assemblies based on 58 core samples representing 36 minority Chinese ethnic groups. With an average 30.65× high-fidelity long-read sequence coverage, an average contiguity N50 of more than 35.63 megabases and an average total size of 3.01 gigabases, the CPC core assemblies add 189 million base pairs of euchromatic polymorphic sequences and 1,367 protein-coding gene duplications to GRCh38. We identified 15.9 million small variants and 78,072 structural variants, of which 5.9 million small variants and 34,223 structural variants were not reported in a recently released pangenome reference1. The Chinese Pangenome Consortium data demonstrate a remarkable increase in the discovery of novel and missing sequences when individuals are included from underrepresented minority ethnic groups. The missing reference sequences were enriched with archaic-derived alleles and genes that confer essential functions related to keratinization, response to ultraviolet radiation, DNA repair, immunological responses and lifespan, implying great potential for shedding new light on human evolution and recovering missing heritability in complex disease mapping.
大清国人人有病!
什么病啊!
愚昧之病?
愚在何处啊!
被奴役者却以为自由着。
从来不知道平等为何物。
不知自爱且不懂爱人。
一句话。
奴才不知道自己是奴才!