Download pages: v1v2v3 • v3 unmerged • Study data

Download unmerged data

Some tissues have RNA-seq datasets from multiple studies that were merged for the v3 release. This page contains input files and results for those individual datasets run without merging.

Gene expression

log2(readcount+1) Used to compute allelic fold change

NAcc1NAcc2NAcc3PL1PL2PL3

TPM (transcripts per million) Relative abundance of transcripts

NAcc1NAcc2NAcc3PL1PL2PL3

Inverse-quantile normalized

NAcc1NAcc2NAcc3PL1PL2PL3

Filtered inverse-quantile normalized Used for eQTL mapping

NAcc1NAcc2NAcc3PL1PL2PL3


Other info

Rat IDs The final QC-filtered sample sets used for eQTL mapping

NAcc1NAcc2NAcc3PL1PL2PL3

RNA-Seq FASTQ file lists with corresponding rat IDs
Each line includes one FASTQ path for single-end reads, or two FASTQ paths for paired-end reads, followed by the rat ID. FASTQ maps can include a mix of single-end and paired-end rows. These files may include mappings to samples that were filtered out during QC, so use the rat ID lists above to get the final sample sets.

NAcc1NAcc2NAcc3PL1PL2PL3

Covariates used for eQTL mapping

NAcc1NAcc2NAcc3PL1PL2PL3


eQTLs

Conditionally independent cis-eQTLs
A table of cis-eQTLs from all tissues.

All significant cis-eQTL variant-gene pairs

NAcc1NAcc2NAcc3PL1PL2PL3

trans-eQTLs
All SNP-gene associations genome-wide with TSS distance > 5 Mb and with an arbitrary cutoff of p < 1e-5. No significance testing was performed.

NAcc1NAcc2NAcc3PL1PL2PL3


sQTLs

Splice phenotypes Relative usage of splice junctions within junction clusters

NAcc1NAcc2NAcc3PL1PL2PL3

Covariates used for sQTL mapping

NAcc1NAcc2NAcc3PL1PL2PL3

All significant cis-sQTL variant-phenotype pairs

NAcc1NAcc2NAcc3PL1PL2PL3

trans-sQTLs
All SNP-phenotype associations genome-wide with TSS distance > 5 Mb and with an arbitrary cutoff of p < 1e-5. No significance testing was performed.

NAcc1NAcc2NAcc3PL1PL2PL3