Table 2. Discovery of variants across 52 genotypes in the collection.
Metric | Count |
---|---|
Number of accessions in the Apios collection | 52 |
Total number of reads generated | 1,315,730,442 |
Average number of reads generated per accession | 25,302,509 |
Average % of reads mapped to the assembly per accession | 89.5 |
Average % of reads mapped uniquely to the assembly per accession | 61.4 |
Number of variants (SNP and Indels) identified with base criteria | 1,582,730 |
Number of variants identified (base criteria + read depth ≥ 5) | 299,145 |
Number of SNPs identified (base criteria + read depth ≥ 5) | 271,170 |
Number of SNPs (base criteria + read depth ≥ 5 + MAF ≥ 0.1 + Maximum missing percentage ≤ 10%) | 58,154 |
Average % reproducibility of SNPs (tested using 4 biological replicates) | 90.6 |
Number of components (a.k.a genes) harboring SNPs | 9,338 |
% of components in the assembly harboring SNPs | 19.2 |
Average accessions missing per SNP (%) | 1.5 |
Average heterozygous accessions per SNP (%) | 37.5 |
Number of gene expression markers identified | 39,609 |
Base criteria: At least 2 reads calling variant within at least 1 accession; ≥20% of the reads calling the variant allele in that sample; and average quality of bases calling the variant is ≥10).