Data in BriefGenetic & Genomic MedicinePeer-reviewed journal article
Datasets for a Simulated Family-Based Exome-Sequencing Study
Abstract
We present simulated exome-sequencing data for 150 families from a North American admixed population, ascertained to contain at least four members affected with lymphoid cancer. These data include information on the ascertained families as well as single-nucleotide variants on the exome of affected family members. We provide a brief overview of the simulation steps and links to the associated software scripts. The resulting data are useful to identify genomic patterns and disease inheritance in families with multiple disease-affected members. Specifications Table O_TBL View this table: org.highwire.dtl.DTLVardef@10720b4org.highwire.dtl.DTLVardef@f4381corg.highwire.dtl.DTLVardef@18fcf5forg.highwire.dtl.DTLVardef@77a038org.highwire.dtl.DTLVardef@1b7c914_HPS_FORMAT_FIGEXP M_TBL C_TBL
- organism: human
- assay: whole-exome sequencing
- research focus: benchmarking
- research focus: variant calling
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: simulation
- Citations
- 0
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