Additional file 7: Table S6. Variants identified by the array-based CGH approach. This table provides details on variants identified using the array-based CGH approach for 17 animals compared to whole-genome sequencing variants
Genomic structural variation is an important and abundant source of genetic and phenotypic variation...
Genomic structural variation is an important and abundant source of genetic and phenotypic variation...
Additional file 2: Table S2. Number of variants included within confidence intervals for each QTL re...
International audienceAbstractBackgroundCopy number variations (CNV) are known to play a major role ...
Additional file 7. Results of GO enrichment. GO enrichment analyses were performed using the MouseMi...
Additional file 4. List of LoF and deleterious missense variants for which no homozygous individual ...
Additional file 7. Accuracy and sensitivity of sequence variant genotyping on bovine chromosome 25 f...
Additional file 6. Frequency of the alternative allele of SNPs in our validation panel. (Sheet 1) Fr...
Additional file 5. GO enrichment analysis using the Cytoscape ClueGO plugin. The results of GO enric...
Background: In recent years, several bovine genome sequencing projects were carried out with the aim...
Additional file 1. Instruction to compile a Graphtyper version modified for the cattle chromosome c...
Additional file 2. Properties of the different metrics used for the evaluation of sequence variant g...
Additional file 6. Comparison of variant filtration using either GATK hard filtering or GATK VQSR
Additional file 3. Concordance of heterozygous and alternate homozygous genotypes in 49 Original B...
The aim of the present study was to identify copy-number variations (CNVs) in Cinisara (CIN) and Mod...
Genomic structural variation is an important and abundant source of genetic and phenotypic variation...
Genomic structural variation is an important and abundant source of genetic and phenotypic variation...
Additional file 2: Table S2. Number of variants included within confidence intervals for each QTL re...
International audienceAbstractBackgroundCopy number variations (CNV) are known to play a major role ...
Additional file 7. Results of GO enrichment. GO enrichment analyses were performed using the MouseMi...
Additional file 4. List of LoF and deleterious missense variants for which no homozygous individual ...
Additional file 7. Accuracy and sensitivity of sequence variant genotyping on bovine chromosome 25 f...
Additional file 6. Frequency of the alternative allele of SNPs in our validation panel. (Sheet 1) Fr...
Additional file 5. GO enrichment analysis using the Cytoscape ClueGO plugin. The results of GO enric...
Background: In recent years, several bovine genome sequencing projects were carried out with the aim...
Additional file 1. Instruction to compile a Graphtyper version modified for the cattle chromosome c...
Additional file 2. Properties of the different metrics used for the evaluation of sequence variant g...
Additional file 6. Comparison of variant filtration using either GATK hard filtering or GATK VQSR
Additional file 3. Concordance of heterozygous and alternate homozygous genotypes in 49 Original B...
The aim of the present study was to identify copy-number variations (CNVs) in Cinisara (CIN) and Mod...
Genomic structural variation is an important and abundant source of genetic and phenotypic variation...
Genomic structural variation is an important and abundant source of genetic and phenotypic variation...
Additional file 2: Table S2. Number of variants included within confidence intervals for each QTL re...