Hi all,
I am using the GTEx cohort, and based on the published datasets, I would like to choose specific genes that are not included in the GTEx_Analysis_v8_eQTL_expression_matrices.tar (which have been completely processed, filtered, and normalized).
Can someone please provide clarification on the necessary steps for me to follow in order to ensure that if I extract the genes of interest from the TPM matrices GTEx_Analysis_2017-06-05_v8_RNASeQCv1.1.9_gene_tpm.gct.gz my gene filters and normalisation will be directly comparable?
Thanks!
1 answer
It looks like the gtex-pipeline repo has info on how the files in GTEx_Analysis_v8_eQTL_expression_matrices.tar were prepared:
eqtl_prepare_expression.py ${tpm_gct} ${counts_gct} ${annotation_gtf} \
${sample_participant_lookup} ${vcf_chr_list} ${prefix} \
--tpm_threshold 0.1 \
--count_threshold 6 \
--sample_frac_threshold 0.2 \
--normalization_method tmm
https://github.com/broadinstitute/gtex-pipeline/blob/master/qtl/eqtl_prepare_expression.wdl
https://github.com/broadinstitute/gtex-pipeline/tree/master/qtl
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Directly comparable to what? What analysis do you want to perform?
I would like to conduct eQTL analysis on certain genes that are not included in the GTEx_Analysis_v8_eQTL_expression_matrices.tar. Therefore, I need to extract these genes from the GTEx_Analysis_2017-06-05_v8_RNASeQCv1.1.9_gene_tpm.gct.gz. I am not sure about the steps I need to take to process/normalize the TPMs.
I am sorry if this is a very basic question, but I cannot find anything on the GTEx portal.