NA12878 WES Benchmark dataset

This dataset makes available the UCSC Genome Browser (genome.ucsc.edu) GRCh37 genome build public session <strong>NA12878 WES Benchmark </strong>files in a single dataset so that these files can be used in other applications or genome browsers such as IGV. The "Procedure and datasets to cross-reference OMIM genes with the genomic regions of interest" Galaxy page on <strong>usegalaxy.org</strong> server's <em><strong>Shared Data Pages</strong></em> describes practical procedure and several possible use cases for this data set. This page can be accessed freely by users logged into their accounts on usegalaxy.org. Please register if you don't have an account on usegalaxy.org Galaxy server. All genomic variant calls in all VCF files of this data set were decomposed and normalized with vt. This dataset contains: Genome in a bottle (GIAB) version 3.3.2 high confidence (HC) variant calls and genomic regions for HapMap individual NA12878 : GIAB_v3.3.2_NA12878-decomposed-normalized.vcf.gz GIAB_v3.3.2_NA12878-decomposed-normalized.vcf.gz.tbi GIAB_v3.3.2_NA12878_HC_regions.bed HapMap individual NA12878 WES variant calls (VCF) and capture regions (BED) from diagnostic laboratories : ARUP whole exome sequencing data (HiSeq 2000) publically available from NCBI GeT-RM Browser converted_ARUP_NA12878_Exome-decomposed-normalized.vcf.gz converted_ARUP_NA12878_Exome-decomposed-normalized.vcf.gz.tbi ARUP_SeqCap_EZ_Exome.bed UCSF whole exome sequencing data (HiSeq 2500) publically available from NCBI GeT-RM Browser converted_UCSF_NA12878_WES_Agilent_V4_Custom-decomposed-normalized.vcf.gz converted_UCSF_NA12878_WES_Agilent_V4_Custom-decomposed-normalized.vcf.gz.tbi UCSF_WES_Agilent_V4_Custom.bed Whole exome data (NextSeq 500) sequenced in CHEO diagnostic laboratory CHEO_NA12878_WES_S1dataset.vcf.gz CHEO_NA12878_WES_S1dataset.vcf.gz.tbi Agilent_CRE_v2.bed Genomic coordinates (BED) of OMIM genes for which a molecular basis of the associated disease is known (as of September 2019) : Omim_Genes.bed