SNPitty: An intuitive web-application for interactive B-allele frequency and copy-number visualization of next generation sequencing data.
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下载链接：
https://www.omicsdi.org/dataset/eva/PRJEB21914
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资源简介：
Development of the web-application SNPitty that allows interactive visualization and interrogation of Variant Call Format (VCF) files by utilizing B-allele frequencies (BAF) of single nucleotide polymorphisms (SNPs), coverage metrics and copy-numbers.
创建时间：
2017-12-13
