<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Riner AN</submitter><funding>NHGRI NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>e171-e178</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12203564</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>54(3)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Black/African American (B/AA) pancreatic ductal adenocarcinoma (PDAC) patients have worse clinical outcomes than White patients and are underrepresented in genomic databases. We aimed to expand our understanding of the PDAC somatic landscape from a diverse cohort.&lt;h4>Materials and methods&lt;/h4>Formalin-fixed paraffin-embedded specimens from 24 surgically resected PDAC cases were collected, with self-reported race/ethnicity. Whole exome sequencing was performed on malignant and benign tissue. Bioinformatics analysis included deduction of genetic ancestry and somatic mutational analysis, with comparisons to public datasets.&lt;h4>Results&lt;/h4>Out of 24 cases, 17 identified as B/AA race; genetic ancestry analysis confirmed proportions of Sub-Saharan African ancestry greater than</pubmed_abstract><journal>Pancreas</journal><pubmed_title>Somatic Genomic Profiling of Pancreatic Ductal Adenocarcinomas From a Diverse Cohort of Patients.</pubmed_title><pmcid>PMC12203564</pmcid><funding_grant_id>U54 CA233465</funding_grant_id><funding_grant_id>R01 CA242003</funding_grant_id><funding_grant_id>U54 CA233396</funding_grant_id><funding_grant_id>P30 CA014089</funding_grant_id><funding_grant_id>P30 CA247796</funding_grant_id><funding_grant_id>T32 HG008958</funding_grant_id><funding_grant_id>U54 CA233444</funding_grant_id><pubmed_authors>Qian J</pubmed_authors><pubmed_authors>Carpten JD</pubmed_authors><pubmed_authors>Herremans KM</pubmed_authors><pubmed_authors>Reams R</pubmed_authors><pubmed_authors>Akki A</pubmed_authors><pubmed_authors>Velazquez-Villarreal EI</pubmed_authors><pubmed_authors>Loza D</pubmed_authors><pubmed_authors>Jin Y</pubmed_authors><pubmed_authors>Riner AN</pubmed_authors><pubmed_authors>George TJ</pubmed_authors><pubmed_authors>Stern MC</pubmed_authors><pubmed_authors>Redda K</pubmed_authors><pubmed_authors>Chamala S</pubmed_authors><pubmed_authors>Craig DW</pubmed_authors><pubmed_authors>Agyare E</pubmed_authors><pubmed_authors>Rajpara S</pubmed_authors><pubmed_authors>Wilkie DJ</pubmed_authors><pubmed_authors>Han B</pubmed_authors><pubmed_authors>Odedina FT</pubmed_authors><pubmed_authors>Trevino JG</pubmed_authors><pubmed_authors>Williams TM</pubmed_authors><pubmed_authors>Raj R</pubmed_authors><pubmed_authors>Hughes SJ</pubmed_authors><pubmed_authors>Merchant N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Somatic Genomic Profiling of Pancreatic Ductal Adenocarcinomas From a Diverse Cohort of Patients.</name><description>&lt;h4>Objectives&lt;/h4>Black/African American (B/AA) pancreatic ductal adenocarcinoma (PDAC) patients have worse clinical outcomes than White patients and are underrepresented in genomic databases. We aimed to expand our understanding of the PDAC somatic landscape from a diverse cohort.&lt;h4>Materials and methods&lt;/h4>Formalin-fixed paraffin-embedded specimens from 24 surgically resected PDAC cases were collected, with self-reported race/ethnicity. Whole exome sequencing was performed on malignant and benign tissue. Bioinformatics analysis included deduction of genetic ancestry and somatic mutational analysis, with comparisons to public datasets.&lt;h4>Results&lt;/h4>Out of 24 cases, 17 identified as B/AA race; genetic ancestry analysis confirmed proportions of Sub-Saharan African ancestry greater than</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-16T23:36:45.565Z</modification><creation>2026-07-12T03:11:30.528Z</creation></dates><accession>S-EPMC12203564</accession><cross_references><pubmed>39999309</pubmed><doi>10.1097/mpa.0000000000002408</doi><doi>10.1097/MPA.0000000000002408</doi></cross_references></HashMap>