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. 2020 Mar 25;9:e51243. doi: 10.7554/eLife.51243

Table 1. Summary of the hybrid analysis.

Category ID Description Interpretation # Samples Fraction of samples Sample identities
Initial definition of the 53 (35%) putative hybrids A1 ‘High’ genome-wide heterozygosity (>=0.004) initial indicator for putative hybrids 46 30% BPK157A1, BUMM3, CH32, CH34, CUK10, CUK11, CUK12, CUK2, CUK3, CUK4, CUK5, CUK6, CUK7, CUK8, CUK9, EP, GE, GEBRE1, GILANI, Inf055, Inf152, ISS174, ISS2426, ISS2429, LdonLV9, LEM3472, LRC-L53, LRC-L61, LRC-L740, Malta33, MAM, SUDAN1, SUKKAR2, 1026–8, 1S, 356WTV, 363SKWTI, 364SPWTII, 38-UMK, 383WTI, 45-UMK, 452BM, 597–2, 597LN, 762L, 855–9
A2 ‘Admixed’ between groups (admixture analysis) initial indicator for putative hybrids 15 10% BPK512A1, CH32, CH34, CL-SL, EP, GE, Inf152, L60b, LEM3472, LRC-L1311, LRC-L1312, LRC-L1313, LRC-L740, MAM, OVN3
Detailed investigation of the 53 (35%) putative hybrids B1 Heterozygous sites distributed relatively evenly across the genome and allele frequency profiles match coverage based somy estimates putative patterns of sexual crossing (F1/F2+), however, cannot be verified without identified putative parents; alternative explanation could be new mutations that are dominating the sample population through a recent bottleneck (e.g. cloning) 18 12% Inf055, GEBRE1, LdonLV9, LRC.L61, SUDAN1, 1026–8, 1S, 356WTV, 363SKWTI, 364SPWTII, 38-UMK, 383WTI, 45-UMK, 452BM, 597–2, 597LN, 762L, 855–9
 B2 Evidence for parents between different groups (or between two distinct strains as previously shown for the CUK samples) alternating in the genome in a block like pattern putative patterns of sexual crossing (F2+), that is ‘hybrids’ 16 (+1) 10% (11%) CH32, CH34, CUK10, CUK11, CUK12, CUK2, CUK3, CUK4, CUK5, CUK6, CUK7, CUK8, CUK9, EP, GE, LEM3472, (LRC-L740)
 B3 Extreme allele frequency variants only mixture of two different high versus low frequency clones or low frequency new mutations distributed across haplotypes in the sample 7 5% BPK157A1, Inf152, ISS174, ISS2426, ISS2429, LRC-L53, MAM
 B4 Intermediate peak allele frequency distributions including extreme frequency peaks mixture of scenarios B1 and B3, that is as B3 but high frequency clone has heterozygous sites itself 4 3% BUMM3, LRC-L740, Malta33, SUKKAR2
 B5 no clear peak pattern of allele frequencies (several peaks at atypical frequencies) mixture of several clones 1 0.01% GILANI
 B6 to few heterozygous sites present to draw further conclusions beyond admixture results signatures are shadowed by too little segregating variation 7 5% BPK512A1, CL-SL, L60b, LRC-L1311, LRC-L1312, LRC-L1313, OVN3