No phenotype name specified, defaulting to 'outcome'.Error in[[<-.data.frame(*tmp*, type, value = "outcome") : replacement has 1 row, data has 0 这个报错来自“TwoSampleMR”包。 报错原因是exposure和outcome没有重合的SNP位点。
A machine learning approach for phenotype name recognition . In: Proceedings of Coling . Mumbai; 2012: p.1425-1440.M. Khordad, R. E. Mercer, and P. Rogan, "A machine learning approach for phenotype name recognition," in Proceedings of COLING, 2012, pp. 1425-1440....
Also, you need to generate a custom json (pheweb_import.fix_json.custom_json) with additional information per sumstat (n_cases/n_controls, phenotype name, description). Example how to generate that json from R7 with the help ofcreate_custom_json.py: gsutil cp gs://finngen-production-libr...
but redirect to # servername instead to make sure only one user session # is created (tomcat will create one user session per # domain which may lead to two (or more) usersessions # depending on the number of serveraliases) # see gscf ticket #321 RewriteCond %{HTTP_HOST} ^test.gscf....
(2018) 8:3564 | DOI:10.1038/s41598-018-21992-9 7 www.nature.com/scientificreports/ Gene name Hsd11b3 Fgf20b Gsdf Rarab Cyp11a2 Hdac11 KAT2b Nr3c2 Amhr2 Fgf9 Esr1/Er Pdgfaa1 Srd5a2 Gene description 11β-Hydroxysteroid dehydrogenase type 3 Fibroblast growth factor 20-like/b Gonadal ...
New phenotypes can be defined by assigning the system-default and user-defined key point name in the combo box. Length between two points, angle between three points, and area among three points can be defined as new phenotypes in 3DPheoFish. Figure 6 A: Main point cloud image viewer. B...
Conditions which have been well-defined clinically in the past may be known by an eponymous name such as Noonan syndrome [24]. However, this naming system does not reflect the molecular basis of disease. This is especially true for conditions such as Noonan, where a similar phenotype is now...
What is another name for heterozygous? In this page you can discover 11 synonyms, antonyms, idiomatic expressions, and related words for heterozygous, like:homozygous, genotype, allele, recessive, MTHFR, C282Y, rb1, heterozygote, premutation, wild-type and homozygote. ...
The nomenclature of Human Genome Variation Society guidelines (http://www.hgvs.org) was used to name the identified mutations. Mutations associated with known WS genes were detected and classified as pathogenic or likely pathogenic according to the American College of Medical Genetics and Genomics ...
NAMESPACE PheGen.Rproj README.md Repository files navigation README GPL-3.0 license PheGen Phenotype Simulator Installation You can install the released version of APGD from Github with: devtools::install_github("Julia-lirong/PheGen") library(PheGen) Reference Lirong Zhu, Shuanglin Zhang, Qi...