FULA 1 IonXpressRNA_004 run184/R_2015_05_14_12_15_30_user_ION-184-DrStathopoulos_150514_NKRNAseq_GSR1-4.GSR1-FULA1.IonXpressRNA_004.fastq BULA 1 IonXpressRNA_011 run184/R_2015_05_14_12_15_30_user_ION-184-DrStathopoulos_150514_NKRNAseq_GSR1-4.GSR4-BULA1.IonXpressRNA_011.fastq BULA 2 IonXpressRNA_012 run185/R_2015_05_15_12_20_11_user_ION-185-DrStathopoulos_150515_NKRNAseq_GSR5-6.GSR5-BULA2.IonXpressRNA_012.fastq BELA 1 IonXpressRNA_013 run185/R_2015_05_15_12_20_11_user_ION-185-DrStathopoulos_150515_NKRNAseq_GSR5-6.GSR6-BELA1.IonXpressRNA_013.fastq FULA 2 IonXpressRNA_006 run186/R_2015_05_21_11_36_50_user_ION-186-DrStathopoulos_150521_NKRNAseq_GSR2-7.GSR2-FULA1.IonXpressRNA_006.fastq BELA 2 IonXpressRNA_014 run186/R_2015_05_21_11_36_50_user_ION-186-DrStathopoulos_150521_NKRNAseq_GSR2-7.GSR7-BELA2.IonXpressRNA_014.fastq FULA 3 IonXpressRNA_010 run187/R_2015_05_22_13_04_56_user_ION-187-DrStathopoulos_150522_NKRNAseq_GSR3-8.GSR3-FULA3.IonXpressRNA_010.fastq FVB Trachea IonXpressRNA_015 run187/R_2015_05_22_13_04_56_user_ION-187-DrStathopoulos_150522_NKRNAseq_GSR3-8.GSR8-FUBtrachea.IonXpressRNA_015.fastq CULA IonXpress_016 run277/R_2016_03_08_13_22_40_user_IONAS-277-ITlab_DrStath_160308_ChIP-RNA_ITC112-113_GSR10.GSR10-P53FllFl.IonXpress_016.fastq Balb/c IonXpressRNA_014_rawlib.basecaller run268/R_2016_01_29_13_01_36_user_IONAS-268-GSR9_GSkP4-5_GKLex1-4_160129.GSR9-mTECsBalbc.IonXpressRNA_014.fastq The samples pending are FELA1 and FELA2. So in total, we will have data on FULA cells (n=3), BULA cells (n=2), BELA cells (n=2), FELA cells (n =2), CULA cells (n=1), and benign tracheal cells (n=2, one from each FVB and BALB/c strains, samples FVB Trachea IonXpressRNA_015 and Balb/c IonXpressRNA_014_rawlib.basecaller). The names of these cell lines have 4 parts: The first letter indicates the mouse strain of origin (C, C57BL/6; F, FVB; B, Balb/c), the second the carcinogen used (U, urethane; E, DEN), LA denotes lung adenocarcinoma, and the number their series of derivation from different mice. The comparisons of gene expression we want to do are: I) Each of the five different tumor cell categories compared with benign samples by unpaired student's t-test and a cutoff of 2. II) A comparison by strain, ie, FULA and FELA cells (n=5) compared with BULA and BELA cells (n=4) of all genes and of only the genes emerging from I. III) A comparison by carcinogen, ie, FULA and BULA and CULA cells (n=6) compared with FELA and BELA cells (n=4) of all genes and of only the genes emerging from I. reczko@max:/data/images/proton/StathopoulosLab/lung$ ../../rnaSeq-pip6fast-mm10.sh reczko@max:/data/images/proton/StathopoulosLab/lung$ ./pip.sh &> pip.log & #@ 3UTRseq the.contrasts.1 <- c( "Benign_vs_FULA", "Benign_vs_BULA", "Benign_vs_BELA", "Benign_vs_CULA" ) the.path="/data/images/proton/StathopoulosLab/lung/www" metaseqr( sample.list=file.path(the.path,"targets.txt"), contrast=the.contrasts.1, annotation="download", org="mm10", refdb="refseq", normalization="deseq", statistics="deseq", fig.format=c("png","pdf"), export.where=file.path(the.path,"metaseqr_StathopoulosLab_lung"), restrict.cores=0.5, qc.plots=c( "mds","biodetection","countsbio","saturation","readnoise","filtered", "correl","pairwise","boxplot","gcbias","lengthbias","meandiff", "meanvar","biodist","volcano","deheatmap" ), exon.filters=NULL, gene.filters=list( length=list( length=500 ), avg.reads=list( average.per.bp=100, quantile=0.25 ), expression=list( median=TRUE, mean=FALSE, quantile=NA, known=NA, custom=NA ), biotype=get.defaults("biotype.filter","hg19") ), pcut=0.05, export.what=c("annotation","p.value","adj.p.value","fold.change", "counts","flags"), export.scale=c("log2","rpgm"), export.values="normalized", export.counts.table=TRUE, report.top=0.05 ) targets_carcinogen FULAandBULAandCULA_vs_BELA targets_strain BULAandBELA_vs_FULA