Primer pair sequences, restriction enzymes, annealing temperature (AT) and amplicon size used for genotyping the mutations CAPN1:c.344G > A and KCNJ10:c.627C > G by PCR-RFLP are given. Primer pair sequences, annealing temperature (AT) and amplicon size of PCR for genotyping the mutation KCNJ10:g.22141027insC validated on a LI-COR 4300 DNA Analyzer as well as primer pair sequences and product-sizes for Sanger sequencing PCR-amplicons of exon 2 and 3 of KCNJ10 are shown. (DOC 57 kb
Time duration required for processing a variable number of cases and controls with the dominant (Dom...
Primer pairs used for Sanger sequencing. Forward and reverse primers for validation of candidate var...
Figure S4. Analysis of the Ikzf2 project. PCR amplification of the genomic region of interest from (...
(A) The genomic sequences of an unaffected and affected Parson Russell Terrier (PRT) are shown. The ...
Variants in the gene KCNJ10 which are private for Parson Russell Terriers (PRT) and Jack Russell Ter...
Sequencing results of nine dogs of different breeds for evaluation of the variants detected in Parso...
Manhattan plot of âlog10 P-values of the genome-wide association study for hereditary ataxia in Pa...
Plot of the first (PCA1) versus the second principal component (PCA2) by hereditary ataxia affected ...
Q-Q-plot of expected âlog10 P-values versus observedâlog10 P-values from the general model analy...
Primer sequences used for validation of the mutation detected by Sanger sequencing. The heterozygous...
Primers (in 5Ⲡto 3Ⲡorientation) and amplification conditions for five gene fragments selected ...
Table S1. Description and accession numbers for canine genomes processed in this study. Indications ...
Primer sequences used for genotyping of candidate SNPs. The two variants located in KRT3 and LEPREL1...
Figure S7. Analysis of the Rapgef5 project. PCR amplification of the genomic region of interest with...
Additional file 1: Figure S1. Landscape of somatic SVs identified in thetumors of 4 dogs. The circle...
Time duration required for processing a variable number of cases and controls with the dominant (Dom...
Primer pairs used for Sanger sequencing. Forward and reverse primers for validation of candidate var...
Figure S4. Analysis of the Ikzf2 project. PCR amplification of the genomic region of interest from (...
(A) The genomic sequences of an unaffected and affected Parson Russell Terrier (PRT) are shown. The ...
Variants in the gene KCNJ10 which are private for Parson Russell Terriers (PRT) and Jack Russell Ter...
Sequencing results of nine dogs of different breeds for evaluation of the variants detected in Parso...
Manhattan plot of âlog10 P-values of the genome-wide association study for hereditary ataxia in Pa...
Plot of the first (PCA1) versus the second principal component (PCA2) by hereditary ataxia affected ...
Q-Q-plot of expected âlog10 P-values versus observedâlog10 P-values from the general model analy...
Primer sequences used for validation of the mutation detected by Sanger sequencing. The heterozygous...
Primers (in 5Ⲡto 3Ⲡorientation) and amplification conditions for five gene fragments selected ...
Table S1. Description and accession numbers for canine genomes processed in this study. Indications ...
Primer sequences used for genotyping of candidate SNPs. The two variants located in KRT3 and LEPREL1...
Figure S7. Analysis of the Rapgef5 project. PCR amplification of the genomic region of interest with...
Additional file 1: Figure S1. Landscape of somatic SVs identified in thetumors of 4 dogs. The circle...
Time duration required for processing a variable number of cases and controls with the dominant (Dom...
Primer pairs used for Sanger sequencing. Forward and reverse primers for validation of candidate var...
Figure S4. Analysis of the Ikzf2 project. PCR amplification of the genomic region of interest from (...