<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(1)</volume><submitter>Raziq MF</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The human gut microbiome has emerged as a potential modulator of treatment efficacy for different cancers, including non-small cell lung cancer (NSCLC) patients undergoing immune checkpoint inhibitor (ICI) therapy. In this study, we investigated the association of gut microbial variations with response against ICIs by analyzing the gut metagenomes of NSCLC patients.&lt;h4>Methods&lt;/h4>Strain identification from the publicly available metagenomes of 87 NSCLC patients, treated with nivolumab and collected at three different timepoints (T0, T1, and T2), was performed using StrainPhlAn3. Variant calling and annotations were performed using Snippy and associations between microbial genes and genomic variations with treatment responses were evaluated using MaAsLin2. Supervised mac</pubmed_abstract><journal>Journal of translational medicine</journal><pagination>343</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11916936</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Prioritizing gut microbial SNPs linked to immunotherapy outcomes in NSCLC patients by integrative bioinformatics analysis.</pubmed_title><pmcid>PMC11916936</pmcid><pubmed_authors>Raziq MF</pubmed_authors><pubmed_authors>Rasool S</pubmed_authors><pubmed_authors>Tariq HMA</pubmed_authors><pubmed_authors>Khan N</pubmed_authors><pubmed_authors>Kayani MUR</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Manzoor H</pubmed_authors><pubmed_authors>Rafiq M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prioritizing gut microbial SNPs linked to immunotherapy outcomes in NSCLC patients by integrative bioinformatics analysis.</name><description>&lt;h4>Background&lt;/h4>The human gut microbiome has emerged as a potential modulator of treatment efficacy for different cancers, including non-small cell lung cancer (NSCLC) patients undergoing immune checkpoint inhibitor (ICI) therapy. In this study, we investigated the association of gut microbial variations with response against ICIs by analyzing the gut metagenomes of NSCLC patients.&lt;h4>Methods&lt;/h4>Strain identification from the publicly available metagenomes of 87 NSCLC patients, treated with nivolumab and collected at three different timepoints (T0, T1, and T2), was performed using StrainPhlAn3. Variant calling and annotations were performed using Snippy and associations between microbial genes and genomic variations with treatment responses were evaluated using MaAsLin2. Supervised mac</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-01T14:40:12.978Z</modification><creation>2025-04-04T00:08:03.916Z</creation></dates><accession>S-EPMC11916936</accession><cross_references><pubmed>40098172</pubmed><doi>10.1186/s12967-025-06370-0</doi></cross_references></HashMap>