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These 16 markers were initially selected from a sample of Spanish individuals, but they were also useful to predict the inversion in individuals of CEU and ASN origin.
All 13,788 markers were initially grouped into 10 linkage groups using MadMapper.
Furthermore these markers were initially designed from genomic sequence of a human B. dermatitidis isolate [ 13].
Markers were initially analyzed to identify any double markers (same retention pattern).
The markers were initially screened for informative segregation using a small screening panel.
SNP markers were initially tested for segregation distortion using the chisq module of TMAP [ 38].
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Since markers are initially undetectable, 0< m j +< m j −≤1.
Markers are initially grouped through pairwise G-tests of independent segregation.
The possible association of OxS markers with levels of BMD and bone markers was initially checked by univariate analysis.
Testing of sex-associated SNP markers was initially performed in all 42 mature F1 plants in the Siirt × Bağyolu population.
For example, distal progenitor markers are initially robustly expressed whereas SFTPC expression is very low across time in HLOs, FOXJ1+ cells do not appear to form mature multi-ciliated structures until placed onto a decelluarized lung matrix and rare SCGB1A1+ cells do not resemble mature club cells.
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