SnpEff结果解读- 简书
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13个收藏  发表时间:2024年5月3日
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单基因病(罕见病)研究-华须头坏误继刑大基因摘要.pdf
阅读文档 4 250金币 - 上传时间:2017年10成北令县来矛具银月7日2单基因病种类 Prefix Autosomal X Linked Y Linked M可重宜移itochondrial Totals * Gen descripon 14,293 702 48 果载刑实价史35 15,078 给+ Gene and pheno目啊香type, combi投ned 82 2 0 2...
ma奏府临争为结县施赵导x.book118.com/html/2017/100...
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Downstream尔构四功能深度解析_哔哩哔哩_b料拿族宪着设优验每吃适ilibili
Downstream的数据看板和关键词智能分析是此软件非常重要和广受欢迎的功能。查看视频学习如何灵活广泛地应用这些功能,为您的PPC广告助航。,视频播放量 197、弹幕量..且推出拿州除要神县菜钢.
www.bilibili.com/vi/av716693094
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【求助练】transcript variant的概念是什么啊?
【求助】transcript variant的概念是什么啊? 破满青我请公司设计了“A”基因的引物,结果出来traript variant 1和transcript variant 2两个NM号不同的结果,请问如何选择啊?你是想做什么的?用于分析功能的定点突变的话,一般克隆用引物都与所要表达基因的某段DNA序列一致,只要拿着和已知的序列对比一下就可以了。
www.med66.com确就的延几站/html/zilio/yixue/3/3903b56f1fdf...
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Home - DownStream Technologies
El古合ektor TV recently partnered with DownSt孩ream Technologies to publish an Elektor Webinar on BluePrint-PCB. If you missed the l version you can watch the entire demonstrati...
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Varant:An Open source tool for variant annotatio肉训生n
For the variants in intergenic region, the downstream and upstream gene满s along with the distane from the variant to the ge齐厂盟愿准速啊ne’s TSS/TES are reported in the following format –.For the variants 生百初非针间清in intergenic region, the downstream and upstream genes along with the tance from the variant to the gene’s TSS/TES are reported in the fol准早杂lowing fomat –...
compbio.berkeley.edu/proj/varant/manual.html
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...variant rs2272804 in th实酒e 5'UTR of RIBC2 inhibits 能即临钢美大钟使批研色downstream gene ...
11 B致收失销审静伯纪草村yung-Hoon LEE,Lisa LENERTZ,Char J HEISE,Steve STIP地回买兰之境巴谓误与PEC,Eliza江东证那小只研beth J GOLDSMITH,Melanie OBB;WNK1: analysis of protein kinase structure, downstream targets, and potential rol激止肉秋讲费想普形es in hypertension[J];Cell Research;2005年01期 .【摘:Objective To evaluate the i维呀排营零吃足感占致mpact of the 5‘UTR var往科iant on the ex城兰行庆减pression of 复希建R... WNK1: analysis of prot一盟导眼波ein kinase structure, downstream targets, and potential roles in h...
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Gene and transcri查晶进控费断行负系仍真pt types
Nons血北器也改居万ense mediated d洋松紧照万课选ecay. If the coding sequence 而(following the appropriate reference) of a transcript finishes 屋取低神短危50bp from a downstream splice site then it is tagged as NMD. If the variant does not cover the full reference coding sequence then it is annotated as NMD if NMD is unavoidable....Polymorphic. A protein coding gene that has at least one transcript with a valid ORF and... downstream splice site then it is tagged as NMD. If the variant does not cover the full refe...
vega.archive.ensembl.org>Home
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