Fig. 2
From: The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes
Data directory tree. The output from the Long Fragment Read (LFR) process consists of a series of files and folders. A complete description of everything contained within the Complete Genomics data package can be found in Additional file 3. ASM assembly, CNV copy number variations, dbSNP Single Nucleotide Polymorphisms database, SV structural variations, VCF variant cell format