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Table 2 Analysis of the Venturia inaequalis genome sequence contigs anchored to the genetic map.

From: Genome-wide SNP identification by high-throughput sequencing and selective mapping allows sequence assembly positioning using a framework genetic linkage map

Sequence contigs size (kb) Total number of sequence contigs Sequence contigs scored and percentage (%) Sequence contigs anchored and percentage (%)
< 20 2461 440 (17.9) 353 (14.3)
20-30 243 175 (72.0) 156 (64.2)
30-40 139 111 (79.9) 75 (54.0)
40-50 75 68 (90.7) 54 (72.0)
50-60 60 54 (90.0) 41 (68.3)
60-70 27 26 (96.3) 20 (74.1)
70-80 22 22 (100.0) 17 (77.3)
80-90 15 14 (93.3) 9 (60.0)
90-100 14 14 (100.0) 9 (64.3)
100-110 11 11 (100.0) 10 (90.9)
110-120 5 4 (80.0) 3 (60.0)
120-130 8 7 (87.5) 6 (75.0)
130-140 4 4 (100.0) 3 (75.0)
> 140 4 4 (100.0) 3 (75.0)
  1. The sequence contigs anchored comprise the contigs for which the joint genotype matches the joint genotype of the pre-determined bins and the contigs for which the bins could be placed into the map. The number of sequence contigs scored and anchored is followed by their respective percentage relative to the total number of sequence contigs indicated in the second column.