<p>This figure exemplifies the HapMap/1000Genomes comparison. Both, frequencies and absolute genotype numbers are reported for each population. A Pearson chi square test checks the concordance with the user’s data. The user can look up the most appropriate HapMap population as well as the super populations from the 1000 Genomes Project and perform an additional plausibility check of the generated genotypes.</p
<p>The data consists in genome-wide SNPs that were obtained from 5 different sources, keeping the SN...
In the current precision medicine era, more and more samples get genotyped and sequenced. Both resea...
A major use of the 1000 Genomes Project (1000GP) data is genotype imputation in genome-wide associat...
Genotypes from the 1000 Genomes reference [1] (v5) were intersected with HapMap3 [2] variants based ...
equilibrium ABSTRACT HapMap samples are currently being genotyped using different high throughput pr...
<p>For the PCL-tumour sample, the variants called by deep sequencing were compared to data from Affy...
One of the goals of the International HapMap Project is the identification of common haplotypes in g...
An increasing number of genome-wide association (GWA) studies are now using the higher resolution 10...
<p>Comparison of genotype and allele frequencies in the control subjects of our study and those from...
An increasing number of genome-wide association (GWA) studies are now using the higher resolution 10...
<p>Concordance rates were based on masking 2% of the genotyped SNPs on chromosome 22 and comparing i...
An increasing number of genome-wide association (GWA) studies are now using the higher resolution 10...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
A hapmap (text) file containing all of the SNPs and their genotypes in each individual that were use...
<p><b>Copyright information:</b></p><p>Taken from "An evaluation of the performance of HapMap SNP da...
<p>The data consists in genome-wide SNPs that were obtained from 5 different sources, keeping the SN...
In the current precision medicine era, more and more samples get genotyped and sequenced. Both resea...
A major use of the 1000 Genomes Project (1000GP) data is genotype imputation in genome-wide associat...
Genotypes from the 1000 Genomes reference [1] (v5) were intersected with HapMap3 [2] variants based ...
equilibrium ABSTRACT HapMap samples are currently being genotyped using different high throughput pr...
<p>For the PCL-tumour sample, the variants called by deep sequencing were compared to data from Affy...
One of the goals of the International HapMap Project is the identification of common haplotypes in g...
An increasing number of genome-wide association (GWA) studies are now using the higher resolution 10...
<p>Comparison of genotype and allele frequencies in the control subjects of our study and those from...
An increasing number of genome-wide association (GWA) studies are now using the higher resolution 10...
<p>Concordance rates were based on masking 2% of the genotyped SNPs on chromosome 22 and comparing i...
An increasing number of genome-wide association (GWA) studies are now using the higher resolution 10...
(SNP) is the most common variation of the human genome with more than 9 million reported in public d...
A hapmap (text) file containing all of the SNPs and their genotypes in each individual that were use...
<p><b>Copyright information:</b></p><p>Taken from "An evaluation of the performance of HapMap SNP da...
<p>The data consists in genome-wide SNPs that were obtained from 5 different sources, keeping the SN...
In the current precision medicine era, more and more samples get genotyped and sequenced. Both resea...
A major use of the 1000 Genomes Project (1000GP) data is genotype imputation in genome-wide associat...