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RAggr finds proxy markers (SNPs and indels) that are in linkage-disequilibrium (LD) with a set of queried markers, using the 1000 Genomes Project and HapMap genotype databases. rAggr uses an expectation maximization algorithm adapted from the Haploview software (Barrett et al., 2005) to calculate pairwise r. And D'. All calculations are done "on the fly" by the web server and are available for one week following job submission. Or database marker IDs. 1000 Genomes, Phase 3, Oct 2014; hg19.

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rAggr | Home | raggr.usc.edu Reviews
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RAggr finds proxy markers (SNPs and indels) that are in linkage-disequilibrium (LD) with a set of queried markers, using the 1000 Genomes Project and HapMap genotype databases. rAggr uses an expectation maximization algorithm adapted from the Haploview software (Barrett et al., 2005) to calculate pairwise r. And D'. All calculations are done on the fly by the web server and are available for one week following job submission. Or database marker IDs. 1000 Genomes, Phase 3, Oct 2014; hg19.
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1 raggr
2 query
3 chromosomal positions
4 options
5 genotypes database
6 populations
7 african
8 americas
9 east asian
10 european
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rAggr | Home | raggr.usc.edu Reviews

https://raggr.usc.edu

RAggr finds proxy markers (SNPs and indels) that are in linkage-disequilibrium (LD) with a set of queried markers, using the 1000 Genomes Project and HapMap genotype databases. rAggr uses an expectation maximization algorithm adapted from the Haploview software (Barrett et al., 2005) to calculate pairwise r. And D'. All calculations are done "on the fly" by the web server and are available for one week following job submission. Or database marker IDs. 1000 Genomes, Phase 3, Oct 2014; hg19.

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rAggr | Help

http://raggr.usc.edu/Help.aspx

Max # Mendel errors. To use rAggr, enter a list of genomic queries into the search box. You may enter rs numbers, marker IDs from the selected genotypes database, or chromosomal positions. A maximum of 500 queries may be entered into the search box at a given time. An rs ID represents one SNP/indel and uses an identifier used by the dbSNP. Position). Positions are based on either hg18 or hg19 depending on the genotypes database selected. Genotypes were downloaded from the IMPUTE2. 3) HapMap Phase II, rel...

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rAggr | About

http://raggr.usc.edu/About.aspx

RAggr is a web-based software program for finding markers (SNPs and indels) that are in linkage-disequilibrium (LD) with a set of queried markers, using the 1000 Genomes Project and HapMap genotype databases. rAggr uses an expectation maximization algorithm adapted from the Haploview software (Barrett et al, Bioinformatics. 2005 Jan 15;21(2):263-5). To calculate pairwise r. And D'. All calculations are done "on the fly" by the web server.

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Linkage disequilibrium - Wikipedia, the free encyclopedia

https://en.wikipedia.org/wiki/Linkage_disequilibrium

From Wikipedia, the free encyclopedia. This article may require cleanup. To meet Wikipedia's quality standards. Has been specified. Please help improve this article. Learn how and when to remove this template message. Is the non-random association of alleles. Loci are said to be in linkage disequilibrium when the frequency of association of their different alleles is higher or lower than what would be expected if the loci were independent and associated randomly. The system of mating. Occurring together ...

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RAggr finds proxy markers (SNPs and indels) that are in linkage-disequilibrium (LD) with a set of queried markers, using the 1000 Genomes Project and HapMap genotype databases. rAggr uses an expectation maximization algorithm adapted from the Haploview software (Barrett et al., 2005) to calculate pairwise r. And D'. All calculations are done "on the fly" by the web server and are available for one week following job submission. Or database marker IDs. 1000 Genomes, Phase 3, Oct 2014; hg19.

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