Citation: Moutsianas L, Agarwala V, Fuchsberger C, Flannick J, Rivas MA, Gaulton KJ, et al. (2015) The Power of Gene-Based Rare Variant Methods to Detect Disease-Associated Variation and Test Hypotheses About Complex Disease. PLoS Genet 11(4): e1005165. https://doi.org/10.1371/jo…
Who's On First | Spelunker | Georgia Georgia uuuu to uuuu 856/331/63/85633163.geojson Georgia is a country and its consensus geometry is derived from whosonfirst Properties {"name:got_x_preferred":["\uD800\uDF32\uD800\uDF34\uD800\uDF30\uD800\uDF3F\uD800\uDF42\uD800\uDF32\uD800\uD…
Subject enrollment In total, 273 subjects were recruited as part of the iPSCORE study, of which 215 subjects have been included in previous studies 39 , 40 , 41 . Data for additional 204 subjects were obtained from the HipSci Collection 42 , 43 . We have complied with all relevan…
{"name:got_x_preferred":["\uD800\uDF39\uD800\uDF3D\uD800\uDF33\uD800\uDF39\uD800\uDF30"],"statoids:marc":"ii","name:ell_x_preferred":["Ινδία"],"ne:su_dif":0,"name:smo_x_variant":["India"],"name:avk_x_preferred":["Barata"],"name:pnb_x_preferred":["ھندستان"],"ne:mapcolor13":2,"name…
Who's On First | Spelunker | Argentina Argentina uuuu to uuuu 856/325/05/85632505.geojson Argentina is a country and its consensus geometry is derived from whosonfirst Properties {"name:got_x_preferred":["\uD800\uDF43\uD800\uDF39\uD800\uDF3B\uD800\uDF31\uD800\uDF3F\uD800\uDF42\uD…
[ RFC Home ] [ TEXT | PDF | HTML ] [ Tracker ] [ IPR ] [ Errata ] [ Info page ] BEST CURRENT PRACTICE Errata Exist Network Working Group A. Phillips, Ed. Request for Comments: 5646 Lab126 BCP: 47 M. Davis, Ed. Obsoletes: 4646 Google Category: Best Current Practice September 2009 …
Network Working Group A. Phillips, Ed. Request for Comments: 5646 Lab126 BCP: 47 M. Davis, Ed. Obsoletes: 4646 Google Category: Best Current Practice September 2009 Tags for Identifying Languages Abstract This document describes the structure, content, construction, and semantics…
RFC 5646 - Tags for Identifying Languages Tags for Identifying Languages RFC 5646 part of BCP 47 Status Email expansions History Document Type RFC - Best Current Practice (September 2009) Errata Obsoletes RFC 4646 Was draft-ietf-ltru-4646bis ltru WG Authors Addison Phillips Mark …
RFC 5646 - Tags for Identifying Languages Network Working Group A. Phillips, Ed. Request for Comments: 5646 Lab126 BCP: 47 M. Davis, Ed. Obsoletes: 4646 Google Category: Best Current Practice September 2009 Tags for Identifying Languages Abstract This document describes the struc…
RFC 5646 - Tags for Identifying Languages Network Working Group A. Phillips, Ed. Request for Comments: 5646 Lab126 BCP: 47 M. Davis, Ed. Obsoletes: 4646 Google Category: Best Current Practice September 2009 Tags for Identifying Languages Abstract This document describes the struc…
RFC 5646: Tags for Identifying Languages RFC Home ] [ TEXT PDF HTML ] [ Tracker ] [ IPR ] [ Errata ] [ Info page BEST CURRENT PRACTICE Errata Exist Network Working Group A. Phillips, Ed. Request for Comments: 5646 Lab126 BCP: 47 M. Davis, Ed. Obsoletes: 4646 Google Category: Best…
Entry - #125310 - CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1; CADASIL1 - OMIM - (OMIM.ORG) #125310 Table of Contents External Links Clinical Resources Clinical Trials EuroGentest Gene Reviews Genetic Alliance MedlinePlus G…
Abstract Whole-genome sequencing harbors unprecedented potential for characterization of individual and family genetic variation. Here, we develop a novel synthetic human reference sequence that is ethnically concordant and use it for the analysis of genomes from a nuclear family…
Abstract Whether neurodegenerative diseases linked to misfolding of the same protein share genetic risk drivers or whether different protein-aggregation pathologies in neurodegeneration are mechanistically related remains uncertain. Conventional genetic analyses are underpowered …
Introduction For many decades after the discovery of the structure of DNA and the genetic code, the field of human genetics was largely focused on understanding the structure and function of protein-coding genes and how rare mutations in these genes cause disease. Indeed, the cen…