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Assembly, variant, and cline data for paper

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DataONE2017-05-12 更新2024-06-26 收录
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This package contains four sets of data: - cline_allele_frequencies: inferred allele frequencies at each SNP (filtered & unfiltered) at each contact zone - probes: probes used in exome capture for each contact zone - target_assemblies: annotated assemblies generated from exome capture data and used as pseudo-reference genome - variants: variant call format files (VCFs) generated by aligning read data from the contact zone to the PRG
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2017-05-12
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