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    <responseDate>2026-10-15T01:02:56Z</responseDate>
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    <identifier>10.57760/sciencedb.0140t</identifier>
    <datestamp>2026-09-29T15:09:26Z</datestamp>
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  <dc:date>2026-09-29</dc:date>
  <dc:title>Analysis code for &amp;quot;Germline causality is not tumour prognosis: dissecting the genetic and prognostic architecture of colorectal cancer in the COADREAD cohort&amp;quot;</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.0140t</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>This dataset contains the complete analysis code underlying the manuscript &amp;quot;Germline causality is&amp;nbsp;not tumour prognosis: dissecting the genetic and prognostic architecture of colorectal cancer in the COADREAD cohort&amp;quot;. The study separates two axes that are routinely fused into a single score: the&amp;nbsp;germline causal axis (whether a gene influences the risk of developing colorectal cancer) and the&amp;nbsp;tumour prognostic axis (whether the expression of that gene in the tumour predicts patient outcome). A 267-gene SNP-related gene set was built by mapping 84 independent risk loci to genes; this set&amp;nbsp;constrained the development of an eight-gene prognostic signature, which was validated across seven&amp;nbsp;external cohorts. A cis-expression quantitative trait locus Mendelian randomisation scan with&amp;nbsp;colocalisation, HEIDI gating, robustness testing (outlier instruments, multivariable Mendelian&amp;nbsp;randomisation, signal-level colocalisation) and druggability assessment was then performed. The&amp;nbsp;archive contains 60 analysis scripts covering preprocessing, genome-wide association study quality&amp;nbsp;control, SNP-to-gene mapping, prognostic modelling, external validation, Mendelian randomisation,&amp;nbsp;colocalisation and figure generation; download helpers for public genome-wide association summary&amp;nbsp;statistics, expression quantitative trait locus resources and Gene Expression Omnibus series; and&amp;nbsp;query scripts for Open Targets, DGIdb, the Human Protein Atlas and the protein quantitative trait&amp;nbsp;locus catalogue. The code is written in R 4.5.3 with a small amount of Python 3.13 for download and&amp;nbsp;query utilities. No third-party dataset is redistributed: all inputs are publicly available and must&amp;nbsp;be obtained from their original sources, as listed in the accompanying README. The analyses used only&amp;nbsp;publicly available summary-level statistics and previously published de-identified data, so ethical&amp;nbsp;approval and informed consent were not required. A single parameter must be edited before running the&amp;nbsp;code: the project root constant BASE at the top of analysis_code/00_core_functions.R. All other&amp;nbsp;paths are derived from it. The random seed is 20260908.</dc:description>
  <dc:subject>colorectal cancer; COADREAD cohort; Mendelian randomisation</dc:subject>
  <dc:creator>Xiao Peng</dc:creator>
  <dc:creator>Tao Angui</dc:creator>
  <dc:creator>Meng Jizeng</dc:creator>
  <dc:creator>Jin Bo</dc:creator>
  <dc:creator>Liu Jianhui</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://api.github.com/licenses/mit</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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