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. 2015 Jun 3;5(7):1463–1472. doi: 10.1534/g3.115.017905

Table 1. Summary of GBS libraries.

Library Barcodes F2s Adapters Total Reads Barcoded F2 Reads Barcoded Reads/F2 Mapped Reads/F2 Mapped Read COV SNP Coverage Marker Coverage Genotype Fail %
1a 48 12 Elshire 216 58.8 4.9 3.1 0.5 3.1 371.7 0.04
2a 48 48 Elshire 212.4 168.3 3.5 2.4 1.03 2.4 288.2 0.5
3 48 48 Elshire 418.6 397.7 8.3 5.6 1.18 0.7 85.1 5.4
4 96 96 Y-shaped 559.7 487.6 5.1 3.9 0.61 3.5 424.7 0.3
5 96 96 Y-shaped 428.2 363.1 3.8 3 0.59 2.8 228.5 1.1
6 96 96 Y-shaped 440.5 371.9 3.9 3 0.61 2.8 230.5 0.9
7b,c 384 332 Y-shaped 498 259.1 0.8 0.6 0.81 0.5 49.1 2.6
All 816 719 * 2773.3 2101.1 2.9 2.2 1.26 1.7 168.6 1.9

For each library, the number of barcodes and F2 fish included is listed. Total reads, barcoded F2 reads, barcoded reads/F2, and mapped reads/F2 are reported in units of millions of reads. Genotype fail % indicates percentage of final genotypes that were missing. COV, coefficient of variance (mean/standard deviation).

a

For libraries 1 and 2, the R2 read failed, resulting in half the expected number of reads.

b

ApeKI digestion and adapter ligation reactions were performed at half volume to conserve costs.

c

Library 7 included nine F2 samples that were sequenced in libraries 1–6 but had very low sequencing coverage.