Statistical analysis and classification of taxa associated with lung cancer

KG K. Leigh Greathouse
JW James R. White
AV Ashely J. Vargas
VB Valery V. Bliskovsky
JB Jessica A. Beck
NM Natalia von Muhlinen
EP Eric C. Polley
EB Elise D. Bowman
MK Mohammed A. Khan
AR Ana I. Robles
TC Tomer Cooks
BR Bríd M. Ryan
NP Noah Padgett
AD Amiran H. Dzutsev
GT Giorgio Trinchieri
MP Marbin A. Pineda
SB Sven Bilke
PM Paul S. Meltzer
AH Alexis N. Hokenstad
TS Tricia M. Stickrod
MW Marina R. Walther-Antonio
JE Joshua P. Earl
JM Joshua C. Mell
JK Jaroslaw E. Krol
SB Sergey V. Balashov
AB Archana S. Bhat
GE Garth D. Ehrlich
AV Alex Valm
CD Clayton Deming
SC Sean Conlan
JO Julia Oh
JS Julie A. Segre
CH Curtis C. Harris
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Statistical analysis and visualization, ANOVA and PCoA, was performed on sequencing quality metrics by population sample type (ImA, HB, NT, and T) (Additional file 1: Figure S1). Alpha- and beta-diversity metrics were computed in QIIME with differential abundance analyses performed in R and Stata (v13). Mann–Whitney tests corrected for multiple testing (Benjamini–Hochberg [FDR]) were used to conduct initial comparisons between tissue type and histological subtype (AD or SCC) followed by multivariable logistic regression controlling for multiple confounders (age, gender, race, smoking status, stage, antibiotic exposure, lung location, average Phred score, and sequencing run) (Additional file 1: Table S11). An additional logistic regression model was constructed to estimate the odds of AD versus SCC for each taxa separately (identified from the initial testing) stratified by TP53 mutation status (wild-type versus mutated) with and interaction term between the taxa and mutation added to the model. See Additional file 1: Supplemental Methods for details of statistical modeling.

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