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          <dc:title>&lt;p&gt;Estimation of LDA coefficients using the entire dataset.&lt;/p&gt;</dc:title>
          <dc:creator>Tomoaki Ueda (1780057)</dc:creator>
          <dc:creator>Kentaro Fukushima (5227799)</dc:creator>
          <dc:creator>Sunggi Chi (25157827)</dc:creator>
          <dc:creator>Hiroshi Haeno (206672)</dc:creator>
          <dc:creator>Goichi Yoshimoto (25157830)</dc:creator>
          <dc:creator>Hironori Arai (10964553)</dc:creator>
          <dc:creator>Daisuke Ikeda (425740)</dc:creator>
          <dc:creator>Motoshi Ichikawa (25157833)</dc:creator>
          <dc:creator>Naoto Takahashi (385073)</dc:creator>
          <dc:creator>Naoko Hosono (9512304)</dc:creator>
          <dc:creator>Takahiro Yamauchi (534724)</dc:creator>
          <dc:creator>Takeshi Kondo (600866)</dc:creator>
          <dc:creator>Shigeru Kusumoto (785749)</dc:creator>
          <dc:creator>Junya Kuroda (81185)</dc:creator>
          <dc:creator>Yosuke Minami (464487)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Cancer</dc:subject>
          <dc:subject>Hematology</dc:subject>
          <dc:subject>Plant Biology</dc:subject>
          <dc:subject>mutational patterns classified</dc:subject>
          <dc:subject>incomplete hematologic recovery</dc:subject>
          <dc:subject>improved overall survival</dc:subject>
          <dc:subject>aml ); however</dc:subject>
          <dc:subject>acute myeloid leukemia</dc:subject>
          <dc:subject>8 %, 52</dc:subject>
          <dc:subject>cri 33 %).</dc:subject>
          <dc:subject>type 1 –</dc:subject>
          <dc:subject>type 1 (&lt;</dc:subject>
          <dc:subject>type 2 framework</dc:subject>
          <dc:subject>type 2 (&lt;</dc:subject>
          <dc:subject>div &gt;&lt; p</dc:subject>
          <dc:subject>differential response patterns</dc:subject>
          <dc:subject>&gt;) groups based</dc:subject>
          <dc:subject>treatment ngs data</dc:subject>
          <dc:subject>azacitidine plus venetoclax</dc:subject>
          <dc:subject>cri following aza</dc:subject>
          <dc:subject>among 53 first</dc:subject>
          <dc:subject>type 1</dc:subject>
          <dc:subject>1 %,</dc:subject>
          <dc:subject>treatment response</dc:subject>
          <dc:subject>effective treatment</dc:subject>
          <dc:subject>≥ third</dc:subject>
          <dc:subject>world cohort</dc:subject>
          <dc:subject>tet2 &lt;/</dc:subject>
          <dc:subject>response heterogeneity</dc:subject>
          <dc:subject>patients treated</dc:subject>
          <dc:subject>nras &lt;/</dc:subject>
          <dc:subject>line settings</dc:subject>
          <dc:subject>line setting</dc:subject>
          <dc:subject>line patients</dc:subject>
          <dc:subject>generation sequencing</dc:subject>
          <dc:subject>frequently observed</dc:subject>
          <dc:subject>cytogenetic analyses</dc:subject>
          <dc:subject>complete remission</dc:subject>
          <dc:subject>clinical variables</dc:subject>
          <dc:subject>clinical determinants</dc:subject>
          <dc:subject>53 genes</dc:subject>
          <dc:description>&lt;p&gt;The preprocessed data were converted to a design matrix using dummy coding for all factors, with the response  coded as 0 for nonCR and 1 for CR. Let  denote the resulting predictor matrix, and let  and  be the mean vectors of the predictors in the nonCR and CR groups, respectively. The within-class covariance matrices  and  were computed for each group, and a pooled within-class covariance matrix, , was then formed, where and are the numbers of nonCR and CR cases. The discriminant weight vector  was obtained as  and prior class probabilities  and  were set equal to the empirical class proportions. The scalar intercept  for the two-group discriminant function was calculated as For each subject with predictor vector , the linear discriminant score was defined as  and classification was given by  for CR and  for nonCR. The elements of  thus quantify the contribution of each standardized predictor to shifting a patient towards the CR or nonCR side of the discriminant boundary.&lt;/p&gt; &lt;p&gt;(DOCX)&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T18:00:01Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1371/journal.pone.0357898.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/_p_Estimation_of_LDA_coefficients_using_the_entire_dataset_p_/34048807</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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