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Merge pull request #610 from d3b-center/OPC_607_SS
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Manual cancer_group assigned for select sample_id with discordant pathology_diagnosis
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jharenza authored Sep 25, 2024
2 parents 73bf9cd + 6203f91 commit 2179329
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Original file line number Diff line number Diff line change
Expand Up @@ -89,6 +89,7 @@ Myeloid Sarcoma NA NA NA
Neuroblastoma EFO_0000621 MONDO_0005072 NCIT_C3270
Neurofibroma/Plexiform EFO_0000658 MONDO_0003304 NCIT_C3797
Non-Hodgkin Lymphoma EFO_0005952 MONDO_0018908 NCIT_C3211
Not Reported NA NA NA
Oligodendroglioma EFO_0000632 MONDO_0016695 NCIT_C3288
Osteosarcoma EFO_0000637 MONDO_0009807 NCIT_C9145
Other tumor NA NA NA
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Expand Up @@ -544,10 +544,22 @@ to_be_classified <- hgg_meta %>%
mutate(molecular_subtype = "HGG, To be classified") %>%
select(Kids_First_Participant_ID, Kids_First_Biospecimen_ID, sample_id, match_id, molecular_subtype)
molecular_subtype_table_final <- all_subtypes %>%
molecular_subtype_table_w_tbc <- all_subtypes %>%
bind_rows(to_be_classified) %>%
arrange(Kids_First_Biospecimen_ID)
# update non DMG brainstem glioma dx to DIPG based on clinical dx for PNOC and Mioncoseq only.
# HGG, IDH remain as HGG
dipgs <- hgg_meta %>%
filter(sub_cohort %in% c("PNOC", "Mioncoseq") &
grepl("Brainstem glioma", pathology_diagnosis)) %>%
select(Kids_First_Biospecimen_ID, primary_site)
molecular_subtype_table_final <- molecular_subtype_table_w_tbc %>%
dplyr::mutate(molecular_subtype = case_when(Kids_First_Biospecimen_ID %in% dipgs$Kids_First_Biospecimen_ID &
grepl("HGG, H3 wildtype|HGG, To be classified", molecular_subtype) ~ gsub("HGG", "DIPG", molecular_subtype),
TRUE ~ molecular_subtype))
# create final lesion + subtype file
lesions_subtypes <- all_data_df %>%
right_join(molecular_subtype_table_final[,c("match_id", "molecular_subtype")]) %>%
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107 changes: 51 additions & 56 deletions analyses/molecular-subtyping-HGG/09-HGG-with-braf-clustering.nb.html

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32 changes: 16 additions & 16 deletions analyses/molecular-subtyping-HGG/10-HGG-TP53-annotation.nb.html
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Expand Up @@ -1512,7 +1512,7 @@
$(this).detach().appendTo(div);

// add a show code button right above
var showCodeText = $('<span>' + (showThis ? 'Hide' : 'Code') + '</span>');
var showCodeText = $('<span>' + (showThis ? 'Hide' : 'Show') + '</span>');
var showCodeButton = $('<button type="button" class="btn btn-default btn-xs btn-secondary btn-sm code-folding-btn pull-right float-right"></button>');
showCodeButton.append(showCodeText);
showCodeButton
Expand All @@ -1538,7 +1538,7 @@
// * Change text
// * add a class for intermediate states styling
div.on('hide.bs.collapse', function () {
showCodeText.text('Code');
showCodeText.text('Show');
showCodeButton.addClass('btn-collapsing');
});
div.on('hidden.bs.collapse', function () {
Expand Down Expand Up @@ -1766,14 +1766,14 @@ <h2>Set up</h2>
<pre class="r"><code># Load in tidyverse functions
library(tidyverse)</code></pre>
<!-- rnb-source-end -->
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<pre><code>── Attaching core tidyverse packages ─────────────────────────────────────────── tidyverse 2.0.0 ──
✔ dplyr 1.1.1 ✔ readr 2.1.4
✔ forcats 1.0.0 ✔ stringr 1.5.0
✔ ggplot2 3.4.2 ✔ tibble 3.2.1
✔ lubridate 1.9.2 ✔ tidyr 1.3.0
✔ purrr 1.0.1
── Conflicts ───────────────────────────────────────────────────────────── tidyverse_conflicts() ──
<!-- rnb-message-begin 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 -->
<pre><code>── Attaching core tidyverse packages ────────────────────────────────────────────────────────────────────── tidyverse 2.0.0 ──
✔ dplyr 1.1.4 ✔ readr 2.1.5
✔ forcats 1.0.0 ✔ stringr 1.5.1
✔ ggplot2 3.5.1 ✔ tibble 3.2.1
✔ lubridate 1.9.3 ✔ tidyr 1.3.1
✔ purrr 1.0.2
── Conflicts ──────────────────────────────────────────────────────────────────────────────────────── tidyverse_conflicts() ──
✖ dplyr::filter() masks stats::filter()
✖ dplyr::lag() masks stats::lag()
ℹ Use the conflicted package (&lt;http://conflicted.r-lib.org/&gt;) to force all conflicts to become errors</code></pre>
Expand Down Expand Up @@ -1804,9 +1804,9 @@ <h3>Required files</h3>
&quot;tp53_altered_status.tsv&quot;), guess_max = 100000) %&gt;%
dplyr::rename(tp53_status = tp53_altered)</code></pre>
<!-- rnb-source-end -->
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<pre><code>Rows: 14307 Columns: 18
── Column specification ───────────────────────────────────────────────────────────────────────────
── Column specification ──────────────────────────────────────────────────────────────────────────────────────────────────────
Delimiter: &quot;\t&quot;
chr (10): Kids_First_Biospecimen_ID, match_id, sample_id, cancer_predisposit...
dbl (8): tp53_score, SV_counts, Fusion_counts, SNV_indel_counts, CNV_loss_c...
Expand All @@ -1819,9 +1819,9 @@ <h3>Required files</h3>
filter(!is.na(pathology_diagnosis),
!cohort %in% c(&quot;TCGA&quot;, &quot;GTEx&quot;))</code></pre>
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<pre><code>Rows: 47895 Columns: 64
── Column specification ───────────────────────────────────────────────────────────────────────────
── Column specification ──────────────────────────────────────────────────────────────────────────────────────────────────────
Delimiter: &quot;\t&quot;
chr (41): Kids_First_Participant_ID, Kids_First_Biospecimen_ID, sample_id, a...
dbl (21): cell_line_passage, OS_days, EFS_days, age_at_diagnosis_days, age_a...
Expand All @@ -1834,9 +1834,9 @@ <h3>Required files</h3>
<pre class="r"><code>hgg_subtypes &lt;- read_tsv(file.path(results_dir,&quot;HGG_cleaned_all_table.tsv&quot;)) %&gt;%
left_join(bs_match)</code></pre>
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<pre><code>Rows: 2155 Columns: 48
── Column specification ───────────────────────────────────────────────────────────────────────────
── Column specification ──────────────────────────────────────────────────────────────────────────────────────────────────────
Delimiter: &quot;\t&quot;
chr (41): Kids_First_Participant_ID, Kids_First_Biospecimen_ID, sample_id, m...
dbl (7): age_at_diagnosis_yr, FOXG1_expression_zscore, OLIG2_expression_zsc...
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Binary file modified analyses/molecular-subtyping-HGG/plots/HGG_stranded.png
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