Willow grouse autosomal heterozygous sites

A vcf file containing the autosomal heterozygous sites of the willow grouse individual. It was generated by the default samtools mpileup and bcftools pipeline. Filtering was performed by vcffilter (from the vcflib suite: https://github.com/ekg/vcflib) to keep only heterozygous sites with read depth between 22 and 136 and mapping quality above 20. Indels were removed by vcftools (v0.1.13), using the '--remove-indels' function.

本数据集为包含柳雷鸟个体常染色体杂合位点的变异检测格式（Variant Call Format，简称VCF）文件。该文件通过默认的samtools mpileup与bcftools分析流程生成。随后使用vcflib工具集（https://github.com/ekg/vcflib）中的vcffilter工具进行过滤，仅保留测序深度介于22至136之间、比对质量值高于20的杂合位点；再通过vcftools（版本v0.1.13）的"--remove-indels"参数移除所有插入缺失变异（Indels）。