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Sample_prot_quan_two_batch_join_qc.params
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Sample_prot_quan_two_batch_join_qc.params
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# SILAC-TMT data processing; parameter file for combining batches
# Author: Surendhar and Abhijit modified:02-07-2024
#Input file
batch1 = /home/adasgupt/Protein_quan_Batch1
batch2 = /home/adasgupt/Protein_quan_Batch2
output_folder = Sample_joined_prot_quan_two_batches #if output_folder already exists, output folder named with suffix "_1" or "_2" or so on will be generated automatically in the same folder where the program excuted;
tmt_reporters_used = sig126; sig127N; sig127C; sig128N; sig128C; sig129N; sig129C; sig130N; sig130C; sig131N; sig131C; sig132N; sig132C; sig133N; sig133C; sig134N
#information of biological replicates and their genotypes
WT1 = b1_sig127N, b1_sig127C, b1_sig128N, b1_sig128C, b1_sig129N
WT2 = b1_sig129C, b1_sig130N, b1_sig130C, b1_sig131N, b1_sig131C
WT3 = b2_sig127N, b2_sig127C, b2_sig128N, b2_sig128C, b2_sig129N
FAD1= b1_sig132N, b1_sig132C, b1_sig133N, b1_sig133C, b1_sig134N
FAD2= b2_sig129C, b2_sig130N, b2_sig130C, b2_sig131N, b2_sig131C
FAD3= b2_sig132N, b2_sig132C, b2_sig133N, b2_sig133C, b2_sig134N
# Outlier removal
free_Lys_ratio = 1, 0.745, 0.637, 0.497, 0.35 # free-Lys measured by independent experiment
free_Lys_outlier = 2 # remove data points faster than free-Lys dynamics;0 = No; 1 = Peptide/Protein level; 2 = change the outlier data points to the same levels of free Lys;
degradation_pattern_outlier = 1 # 0 = No; 1 = at mean Peptide/Protein of three bilogical replicates;remove data points with unusual degradation pattern;
######## END of Parameter file #################