Car_ign_intragenomic_SNP_indel_variation_from_1200bp+_contigs.filtered
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资源简介：
Variant call format (VCF) file containing potential single nucleotide polymorphisms (SNPs) and indels variation extracted from nucleotide contigs >=1,200 bp assembled from 139,329,276 100 bp pair end (PE) reads from an Illumina HiSeq 2000 using Ray v2.0.0 for Caranx ignobilis. The following filters were applied with the program vcf-annotate: –f +/c3,10/Q=20/d=15/D=25. This file contains ONLY SNPs and indels that DID pass filtering.
创建时间：
2014-01-01
