nature.com
A map of human genome variation from population-scale sequencing : Nature : Nature Research
http://www.nature.com/nature/journal/v467/n7319/full/nature09534.html
Jump to main content. International weekly journal of science. Structural biology: A peep through anion channels. Homologue structure of the SLAC1 anion channel for closing stomata in leaves. A map of human genome variation from population-scale sequencing. The 1000 Genomes Project Consortium. View interactive PDF in ReadCube. Data generation, alignment and variant discovery. Power to detect variants. Application to association studies. Mutation, recombination and natural selection. The number of variant...
droog.gs.washington.edu
Nickerson Lab - Tools and Data
http://droog.gs.washington.edu/datatools.html
Genome Variation Server (GVS). Last update December 2015.
snp.gs.washington.edu
SeattleSeq Annotation
http://snp.gs.washington.edu/SeattleSeqAnnotation141/HelpAbout.jsp
Download Example Input Files. SeattleSeq Annot. latest. SeattleSeq Ann. 138 (hg19). The SeattleSeq Annotation server provides annotation of SNVs (single-nucleotide variations) and small indels, both known and novel. This annotation includes dbSNP rs IDs, gene names and accession numbers, variation functions (e.g. missense), protein positions and amino-acid changes, conservation scores, HapMap frequencies, PolyPhen predictions, and clinical association. Please see the terms of service.
diabetes.diabetesjournals.org
Genetic Variation, C-Reactive Protein Levels, and Incidence of Diabetes | Diabetes
http://diabetes.diabetesjournals.org/content/56/3/872
Skip to main content. Standards of Medical Care. BMJ Open Diabetes Research and Care. Follow ada on Twitter. Visit ada on Facebook. Search for this keyword. Online Ahead of Print. Late-Breaking Scientific Sessions Abstracts. Standards of Medical Care. BMJ Open Diabetes Research and Care. Search for this keyword. Online Ahead of Print. Late-Breaking Scientific Sessions Abstracts. Genetic Variation, C-Reactive Protein Levels, and Incidence of Diabetes. Moniek pm de Maat. Andre G. Uitterlinden. CRP is produ...
ldgh.com.br
Links
http://www.ldgh.com.br/index.php/sidemenu-links
Platform for Learning Bioinformatics. The Elements of Bioinformatics. Association tests between sets of SNPs and a phenotype. Tutorial for the linux grep command.
gvs.gs.washington.edu
How to Use GVS
http://gvs.gs.washington.edu/GVS141/HelpHowToUse.jsp
GVS: Genome Variation Server 141. How to Use GVS. How to Use GVS. To use this site, your browser must have cookies and JavaScript enabled. There are 4 steps to access GVS information:. 1 select the search type. 2 select the data source. 3 set query and analysis parameters (optional). 4 choose the results to be displayed. Choose the search type on the home page. There are 3 categories: "search database" (the most common option), "search candidate genes", and "input from file". Database queries give genoty...
egp.gs.washington.edu
NIEHS SNPs Program
http://egp.gs.washington.edu/genotyping_summary_data.html
NIEHS Exome Variant Server. A-Z Finished Genes Directory. Double Strand Break Repair. Summary Data: HTML Table. Summary Data: CSV File. Genotyping Data Bulk Download. WARNING: This is a very large file and may take several minutes to download. The file is a compressed and "tarred" unix file containing the entire directory of text data files. These are the same text data files which appear in the data pages for each candidate gene on our Genes Genotyped. Of all genotyping files.
egp.gs.washington.edu
Personnel
http://egp.gs.washington.edu/personnel.html
NIEHS Exome Variant Server. A-Z Finished Genes Directory. Double Strand Break Repair. Deborah Nickerson, PhD. Mark Rieder, PhD.
egp.gs.washington.edu
Data Download
http://egp.gs.washington.edu/data_download.html
NIEHS Exome Variant Server. A-Z Finished Genes Directory. Double Strand Break Repair. All Phase 1 NIEHS SNPs Variation Data. Of All Variation Data Files. WARNING: This is a very large file and will take several minutes to download. The file is a compressed and "tarred" unix file containing the entire directory of text data files. These are the same text data files which appear in the data pages for each candidate gene in our Finished Genes Table. Please see our Usage Policy. NIEHS SNPs SIFT/PolyPhen Data.
