Describing sequence variants
NOTE: this website is frozen since May 1, 2016. It has been replaced by a new version at http://www.HGVS.org/varnomen. These pages serve as archival copy only. Contents Recent additions HGVS/HVP/HUGO Sequence Variant Description Working Group (SVD-WG) proposals open for comments:Â SVD-WG004 ISCN<>HGVS (open until Jan.15, 2016) decision on previous proposals follow HGVS on Facebook Current recommen
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The majority of the Libido enhancement products come from China. Usually, China manufactures cheap versions of the original products, and it is almost impossible not to find a product that does not have a Cheap Chinese alternative. So, do be astonished when you come across a bottle of libido enhancement selling under $3 online. No wonder you can even find some wholesalers selling a bottle for less
Sanger Team Analyses Suggest Synthetic Associations Not Behind Most Common Disease GWAS Signals
Sanger Team Analyses Suggest Synthetic Associations Not Behind Most Common Disease GWAS Signals By Andrea Anderson COLD SPRING HARBOR, NY (GenomeWeb News) – Synthetic associations between rare, disease-causing variants and common variants probably explain relatively few of the signals detected in genome-wide association studies of common disease, according to Wellcome Trust Sanger Institute human
Disease hunting with whole genome sequences: the good news, and the bad news : Genetic Future
Lupski, J.R., et al. (2010). Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. New England Journal of Medicine advance online 10.1056/nejmoa0908094 Roach, J.C., & et al. (2010). Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science : 10.1126/science.1186802 Two new papers out today - the first ever studies to employ whole-genome sequencing
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deCODE genetics, Inc. Files Voluntary Chapter 11 Petition to Facilitate Sale of Assets Enters into asset purchase agreement and receives commitment for debtor-in-possesion financing to continue operations during Chapter 11 process Reykjavik, ICELAND, November 17, 2009 – deCODE genetics Inc. (Nasdaq:DCGN) today announced that it has filed a voluntary petition for relief under Chapter 11 of the Unit
マイクãƒã‚¢ãƒ¬ã‚¤è§£æž | Thermo Fisher Scientific - JP
日本人ã«ç‰¹åŒ–ã—ãŸApplied Biosystemsâ„¢ Axiomâ„¢ ジャãƒãƒ‹ã‚«ã‚¢ãƒ¬ã‚¤ðŸ„¬ NEO ã•ã¾ã–ã¾ãªäººç¨®ã«å¯¾å¿œã—ãŸAxiom PMDA Arrayãªã© è–¬ç†ã‚²ãƒŽãƒŸã‚¯ã‚¹ç”¨Axiom PharmacoScan, PharmacoFocus Array SARS-CoV-2用ジェノタイピングアレイ Axiom Propel ワークフãƒãƒ¼ã‚½ãƒªãƒ¥ãƒ¼ã‚·ãƒ§ãƒ³ éºä¼å発ç¾è§£æž ジャãƒãƒ‹ã‚«ã‚¢ãƒ¬ã‚¤Â® ã¯å›½ç«‹å¤§å¦æ³•äººæ±åŒ—大å¦ã®ç™»éŒ²å•†æ¨™ã§ã™ã€‚ ジャãƒãƒ‹ã‚«ã‚¢ãƒ¬ã‚¤Â® NEO ã¯ã€Life Technologies Corporation, part of Thermo Fisher Scientific Inc. ãŒæ±åŒ—大å¦ã‚ˆã‚Šãƒ©ã‚¤ã‚»ãƒ³ã‚¹ã‚’å—ã‘ã¦è£½é€ ・販売ã—ã¦ã„ã¾ã™ã€‚ジャãƒãƒ‹ã‚«ã‚¢ãƒ¬ã‚¤Â® NEO ã«æ載ã•ã‚Œã¦ã„る疾患関連 SNP マーカーã¯ã™ã¹ã¦ç ”究用途ã§ã™ã€‚
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Serious flaws revealed in "longevity genes" study : Genetic Future
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http://www.epistasisblog.org/2010/06/common-variants-rare-variants-or-rare.html
http://genepi_toolbox.i-med.ac.at/?page_id=329
Capture and Subassembly with Jay Shendure
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Human Y Chromosome Base-Substitution Mutation Rate Measured by Direct Sequencing in a Deep-Rooting Pedigree
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The Rotterdam Study: 2010 objectives and design update
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