笔记

1、谷歌广告跟踪代码有个https://www.google.com/recaptcha/api2/aframe 接口，打开要22秒，直接导致谷歌人机验证打不开
2、拖垮wordpress网址速度

周一早上参加了华为那边2个人同时面试，面试了1个多小时。
面试的内容比较多，首先自我介绍，然后问了很多关于测试的专业知识，虽然部分答对了，但很多还是不行。还是华为那边人有专业知识。

自从华为外包换项目失败后，也在找工作APP，投递了大量简历。
全部都是没回复，这就意味着可能要一直在华为外包工作，一直换组的那种。

今天全国计算机技术与软件专业技术资格官网开放了在线模拟作答网站。
是Windows安装程序。

1、报错信息（原因） 原因是用脚本卸载，系统上有netdata遗留配置，遗留文件，遗留插件（或者程序）没有卸载 ...

在netdata的GitHub找到的，百度搜索根本搜不到。 ⭕ 原文： 在Linux上使用wget下载netd ...

这次是什么华为什么智能，感觉跟在海康差不多，是在模拟仿真上测试，经常出差。
下周一华为那边2个面试，需要独立负责项目，希望是能面试通过。

🎈-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

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.