Five candidate gene lists, provided as examples for use with
fisher.iteration and candidate.overlap.
Format
A list of five character vectors of official gene symbols:
AutDBHand-curated list of Autism Spectrum Disorder (ASD) candidate genes derived from human genetics studies, downloaded from AutDB (N = 328).
protein.disrupting.rdnvGenes affected by protein-disrupting rare de novo variants in ASD probands, collected from four exome studies published in 2012 (N = 122).
silent.rdnvNegative control: genes affected by silent rare de novo variants in unaffected siblings, from the same four studies (N = 122).
hcrt.genesGenes differentially regulated in narcoleptic mice with hypocretin (Hcrt) neuron ablation versus controls (N = 63).
retinopathy.genesGenes implicated in human congenital retinopathies, from the curated RetNet database (N = 120).
Source
AutDB: Basu SN, Kollu R, Banerjee-Basu S (2009). AutDB: a gene
reference resource for autism research. Nucleic Acids Research
37:D832-D836. doi:10.1093/nar/gkn835
protein.disrupting.rdnv and silent.rdnv:
Iossifov I, Ronemus M, Levy D, et al. (2012). De novo gene disruptions in
children on the autistic spectrum. Neuron 74:285-299.
doi:10.1016/j.neuron.2012.04.009
.
Neale BM, Kou Y, Liu L, et al. (2012). Patterns and rates of exonic de novo
mutations in autism spectrum disorders. Nature 485:242-245.
doi:10.1038/nature11011
.
Sanders SJ, Murtha MT, Gupta AR, et al. (2012). De novo mutations revealed
by whole-exome sequencing are strongly associated with autism.
Nature 485:237-241. doi:10.1038/nature10945
.
O'Roak BJ, Vives L, Girirajan S, et al. (2012). Sporadic autism exomes
reveal a highly interconnected protein network of de novo mutations.
Nature 485:246-250. doi:10.1038/nature10989
.
hcrt.genes: Honda M, Eriksson KS, Zhang S, et al. (2009). IGFBP3
colocalizes with and regulates hypocretin (orexin). PLoS ONE
4:e4254. doi:10.1371/journal.pone.0004254
retinopathy.genes: Daiger SP. RetNet, the Retinal Information
Network. https://web.sph.uth.edu/RetNet/
Examples
data(candidate.genes)
names(candidate.genes)
#> [1] "AutDB" "protein.disrupting.rdnv"
#> [3] "silent.rdnv" "hcrt.genes"
#> [5] "retinopathy.genes"
lengths(candidate.genes)
#> AutDB protein.disrupting.rdnv silent.rdnv
#> 328 122 122
#> hcrt.genes retinopathy.genes
#> 63 120
head(candidate.genes$AutDB)
#> [1] "ABAT" "ADA" "ADK" "ADORA2A" "ADRB2" "ADSL"