allele counts
收藏Mendeley Data2024-01-31 更新2024-06-28 收录
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http://datadryad.org/resource/doi:10.5061/dryad.n136c/4
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资源简介：
This zipped file contains the number of reads matching each of two alternative allels for each indvidual and locus. Loci are delineated by a 'contig' line that gives the fragment number, position of the SNP on the pseudo-reference genome, and the estimated average error probability for the SNP. The other lines begin with an individual id, which is follwed by the number of read of each allele.
创建时间：
2024-01-31
