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Browse files- scripts/parse_mahendrawada.R +58 -41
scripts/parse_mahendrawada.R
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@@ -3,6 +3,12 @@ library(here)
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library(arrow)
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library(readxl)
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# genomic feature harmonization table ----
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# see https://huggingface.co/datasets/BrentLab/yeast_genome_resources
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genomicfeatures = arrow::open_dataset(here("data/genome_files/hf/features")) %>%
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@@ -90,24 +96,6 @@ stopifnot(
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filter(!complete.cases(.) | locus_tag != gene_id) %>%
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nrow() == 0)
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mahedrawada_genomicfeatures %>%
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left_join(genomicfeatures %>%
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select(locus_tag, symbol) %>%
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mutate(gene_id = locus_tag)) %>%
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write_parquet(here("~/code/hf/mahendrawada_2025/features_mahendrawada_2025.parquet"),
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compression = "zstd",
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write_statistics = TRUE,
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use_dictionary = c(
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gene_id = TRUE,
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gene_name = TRUE,
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chr = TRUE,
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locus_tag = TRUE,
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symbol = TRUE,
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coactivator = TRUE
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)
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)
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chec_data_final = chec_data %>%
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left_join(
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genomicfeatures %>%
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@@ -122,18 +110,6 @@ chec_data_final = chec_data %>%
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select(regulator_locus_tag, regulator_symbol, target_locus_tag, target_symbol, peak_score) %>%
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arrange(regulator_locus_tag, target_locus_tag)
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chec_data_final %>%
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write_parquet(here("~/code/hf/mahendrawada_2025/chec_mahendrawada_2025.parquet"),
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compression = "zstd",
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write_statistics = TRUE,
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use_dictionary = c(
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regulator_locus_tag = TRUE,
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regulator_symbol = TRUE,
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target_locus_tag = TRUE,
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target_symbol = TRUE
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)
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)
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rnaseq_data_final = rnaseq_data %>%
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left_join(
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genomicfeatures %>%
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@@ -148,14 +124,55 @@ rnaseq_data_final = rnaseq_data %>%
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select(regulator_locus_tag, regulator_symbol, target_locus_tag, target_symbol, log2fc) %>%
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arrange(regulator_locus_tag, target_locus_tag)
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library(arrow)
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library(readxl)
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# from fetchngs, the multiqc metadata has an easy way to map between
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# accessions and samples
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multqc_chec_config = yaml::read_yaml("~/Downloads/multiqc_config.yml")
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chec_meta <- map_dfr(multqc_chec_config$sample_names_rename,
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~tibble(!!!setNames(., multqc_chec_config$sample_names_rename_buttons)))
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# genomic feature harmonization table ----
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# see https://huggingface.co/datasets/BrentLab/yeast_genome_resources
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genomicfeatures = arrow::open_dataset(here("data/genome_files/hf/features")) %>%
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filter(!complete.cases(.) | locus_tag != gene_id) %>%
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nrow() == 0)
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chec_data_final = chec_data %>%
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left_join(
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genomicfeatures %>%
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select(regulator_locus_tag, regulator_symbol, target_locus_tag, target_symbol, peak_score) %>%
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arrange(regulator_locus_tag, target_locus_tag)
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rnaseq_data_final = rnaseq_data %>%
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left_join(
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genomicfeatures %>%
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select(regulator_locus_tag, regulator_symbol, target_locus_tag, target_symbol, log2fc) %>%
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arrange(regulator_locus_tag, target_locus_tag)
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sample_id_map = tibble(
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regulator_locus_tag = union(rnaseq_data_final$regulator_locus_tag,
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chec_data_final$regulator_locus_tag)) %>%
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mutate(sample_id = row_number())
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# chec_data_final %>%
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# left_join(sample_id_map) %>%
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# select(sample_id, all_of(colnames(chec_data_final))) %>%
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# write_parquet(here("~/code/hf/mahendrawada_2025/chec_mahendrawada_2025.parquet"),
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# compression = "zstd",
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# write_statistics = TRUE,
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# use_dictionary = c(
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# sample_id = TRUE,
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# regulator_locus_tag = TRUE,
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# regulator_symbol = TRUE,
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# target_locus_tag = TRUE,
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# target_symbol = TRUE
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# )
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# )
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#
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# rnaseq_data_final %>%
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# left_join(sample_id_map) %>%
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# select(sample_id, all_of(colnames(rnaseq_data_final))) %>%
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# write_parquet(here("~/code/hf/mahendrawada_2025/rnaseq_mahendrawada_2025.parquet"),
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# compression = "zstd",
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# write_statistics = TRUE,
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# use_dictionary = c(
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# sample_id = TRUE,
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# regulator_locus_tag = TRUE,
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# regulator_symbol = TRUE,
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# target_locus_tag = TRUE,
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# target_symbol = TRUE
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# )
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# )
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#
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# mahedrawada_genomicfeatures %>%
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# left_join(genomicfeatures %>%
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# select(locus_tag, symbol) %>%
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# mutate(gene_id = locus_tag)) %>%
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# write_parquet(here("~/code/hf/mahendrawada_2025/features_mahendrawada_2025.parquet"),
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# compression = "zstd",
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# write_statistics = TRUE,
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# use_dictionary = c(
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# gene_id = TRUE,
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# gene_name = TRUE,
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# chr = TRUE,
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# locus_tag = TRUE,
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# symbol = TRUE,
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# coactivator = TRUE
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# )
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# )
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