- A3 windowed correlations[supplements/466946_file02.csv]
- Supplement[supplements/466946_file03.docx]
- A3 windowed partial correlations[supplements/466946_file04.csv]
- A4 windowed correlations[supplements/466946_file05.csv]
- A4 windowed partial correlations[supplements/466946_file06.csv]
- Table_S1_Genome_wide_windowed_correlations[supplements/466946_file07.csv]
- Table_S2_Genotypes_for_all_markers[supplements/466946_file08.csv]
- Table_S3_all_chromosomes_windowed_correlations[supplements/466946_file09.csv]
- Table_S4_Genome_wide_windowed_partial_correlations[supplements/466946_file10.csv]
- Table_S5_all_chromosomes_windowed_partial_correlations[supplements/466946_file11.csv]
- Table_S7_linear_model results[supplements/466946_file12.xlsx]
- XY_windowed_correlations[supplements/466946_file13.csv]
- XY_windowed_partial_correlations[supplements/466946_file14.csv]
- A1_windowed_correlations[supplements/466946_file15.csv]
- A1_windowed_partial_correlations[supplements/466946_file16.csv]
- A2_windowed_correlations[supplements/466946_file17.csv]
- A2_windowed_partial_correlations[supplements/466946_file18.csv]
Posted November 04, 2021.
Recombination landscape dimorphism contributes to sex chromosome evolution in the dioecious plant Rumex hastatulus
